Pathway aberrations of murine melanoma cells observed in Paired-End diTag transcriptomes
BMC Cancer volume 7, Article number: 109 (2007)
Melanoma is the major cause of skin cancer deaths and melanoma incidence doubles every 10 to 20 years. However, little is known about melanoma pathway aberrations. Here we applied the robust Gene Identification Signature Paired End diTag (GIS-PET) approach to investigate the melanoma transcriptome and characterize the global pathway aberrations.
GIS-PET technology directly links 5' mRNA signatures with their corresponding 3' signatures to generate, and then concatenate, PETs for efficient sequencing. We annotated PETs to pathways of KEGG database and compared the murine B16F1 melanoma transcriptome with three non-melanoma murine transcriptomes (Melan-a2 melanocytes, E14 embryonic stem cells, and E17.5 embryo). Gene expression levels as represented by PET counts were compared across melanoma and melanocyte libraries to identify the most significantly altered pathways and investigate the expression levels of crucial cancer genes.
Melanin biosynthesis genes were solely expressed in the cells of melanocytic origin, indicating the feasibility of using the PET approach for transcriptome comparison. The most significantly altered pathways were metabolic pathways, including upregulated pathways: purine metabolism, aminophosphonate metabolism, tyrosine metabolism, selenoamino acid metabolism, galactose utilization, nitrobenzene degradation, and bisphenol A degradation; and downregulated pathways: oxidative phosphorylation, ATPase synthesis, TCA cycle, pyruvate metabolism, and glutathione metabolism. The downregulated pathways concurrently indicated a slowdown of mitochondrial activities. Mitochondrial permeability was also significantly altered, as indicated by transcriptional activation of ATP/ADP, citrate/malate, Mg++, fatty acid and amino acid transporters, and transcriptional repression of zinc and metal ion transporters. Upregulation of cell cycle progression, MAPK, and PI3K/Akt pathways were more limited to certain region(s) of the pathway. Expression levels of c-Myc and Trp53 were also higher in melanoma. Moreover, transcriptional variants resulted from alternative transcription start sites or alternative polyadenylation sites were found in Ras and genes encoding adhesion or cytoskeleton proteins such as integrin, β-catenin, α-catenin, and actin.
The highly correlated results unmistakably point to a systematic downregulation of mitochondrial activities, which we hypothesize aims to downgrade the mitochondria-mediated apoptosis and the dependency of cancer cells on angiogenesis. Our results also demonstrate the advantage of using the PET approach in conjunction with KEGG database for systematic pathway analysis.
Cancers are caused by multiple genetic and/or epigenetic alterations [1–4]. These alterations include activation of oncogenes, inactivation of tumor suppressor genes, mutations that cause chromosome instability , and mutations that affect key pathways such as apoptosis, MAPK, cell cycle progression, Wnt/β-catenin, metastasis, and angiogenesis [6–9].
Melanomas are among the most common cancers in human and their incidences continue to rise at a pace faster than any other malignancy . Genetic alterations in melanoma signaling pathways have been reported recently [3, 11]; however, global pathway aberrations remain unclear. We applied the robust Gene Identification Signature Paired-End diTag technology (GIS-PET) to reveal the global pathway aberrations in melanoma by using the murine melanoma cell line B16F1 as a model system. B16F1 is a metastatic clone generated from the spontaneous melanoma cell line B16F0. Some in vitro and in vivo studies of this cell line, including deletion in Ink4a/Arf exons and p53 protein expression level, have been well documented and can serve as controls for data validation [12, 13].
Previous transcriptome studies were mostly performed with high throughput microarray or Serial Analysis of Gene Expression (SAGE) approaches. Microarray is a well commercialized technology . It uses mRNAs from a given cell line or tissue to generate a labeled target sample, which is hybridized to a large number of DNA sequences, each representing a gene. The signal intensity of each hybridized DNA sequence is subtracted by a control and analyzed with software packages not only for data processing, but also for mapping gene-expression clusters to integrated pathways . SAGE is another powerful method for studying transcriptome profiles. It extracts short, positionally defined, tag signatures from expressed mRNAs and subsequently correlates the signatures to genomic coordinates using the UniGene virtual database [16, 17]. The SAGE method is also supported by a number of software and public databases which have been made available for cancer studies [18, 19]. Both of these approaches have been applied to melanoma studies. The focuses of these studies, however, were mainly on genes, gene sets, or pathway annotations. To our best knowledge, application of these technologies (or any other technologies) to the global study of melanoma pathway aberrations is presently not available.
GIS-PET was originally developed to facilitate the study of transcriptome profiles. It covalently links the corresponding 5' and 3' signatures of full-length transcripts into PET sequences of around 36 bp (18 bp from each of the 5' and 3' signatures of the same mRNA transcript) and concatenates multiple PETs to form longer stretches of cDNA fragments for high throughput sequencing [20, 21]. We have shown that GIS-PET is able to precisely locate the transcription start sites (TSSs) and the polyadenylation sites (PASs) of expressed genes. When combined with chromatin immunoprecipitation (ChIP) approach, PET method is able to precisely map the genome-wide transcription factor binding sites (TFBSs), as demonstrated in the studies of human tumor suppressor p53  and murine developmental regulators OCT4 and NANOG .
For this investigation, we generated PET transcriptomes from 4 independent but related murine cell types: B16F1 melanoma cells, Melan-a2 melanocytes, E17.5 embryo, and E14 embryonic stem cells. PETs were mapped against University of California at Santa Cruz (UCSC) genome database mm5 and annotated to known genes. The associated genes were subsequently annotated to various pathways using KEGG murine database. We adopted hypergeometric distribution to assess pathway alterations based on a few reasons. First, hypergeometric distribution is one of the most commonly used analytical methods for microarray transcriptome analysis. Although there are differences between PET and microarray technologies, their analytical tools are mutually applicable to a great extent. Secondly, our transcriptome libraries contain large datasets, and variations resulted from the differences in analytical metrics become insignificant for large datasets. Moreover, our libraries do not contain replicates or serial samples collected from different time points and are thus suitable for analysis with the hypergeometric approach.
Because melanocytic cells (including B16F1 and Melan-a2) have the unique capability to produce melanin, while embryonic cells (including E14 stem cells and E17.5 embryo) do not, we first compared the PET counts of melanin biosynthesis genes between melanocytic cells and embryonic cells to ensure the feasibility of using PET count to represent the expression level. Melanogenesis in mice is a complex process involving more than 150 genes located in about 50 loci, which exert functions in various processes including melanin biosynthesis, aggregation and transportation  We focused on melanin biosynthesis because this process has been well characterized. The results strongly support the idea of using a PET approach for pathway comparisons.
We subsequently evaluate the degree of pathway perturbation library-wide using the hypergeometric approach so as to identify the most significantly altered pathways in melanoma cells. We also looked into the pathways previously shown to be implicated in tumorigenesis and identified the transcriptional variants resulted from alternative TSSs or alternative PASs, which may play important roles in melanoma tumorigenesis and pathway aberrations. Our data revealed a systematic redistribution of workload for multiple metabolic pathways leading to an enhanced detoxification capability and a reduction of electron transport chain (ETC) usage through a global downregulation of mitochondria-harbored pathways. In parallel, the revamping was accompanied by shattered tumor suppressor pathways and apoptotic pathways, and redefined mitochondrial permeability. Thus, functional perturbations in multiple molecules, caused by multiple genetic and/or epigenetic alterations, affect multiple metabolic and signal transduction pathways and the combinatorial effect ultimately determines cancer cell survival. Our discoveries should be able to facilitate drug target discoveries for cancer therapy.
As described previously , B16F1 murine melanoma cells were grown in Dulbecco's modified Eagle's medium (DMEM) supplemented with 10% fetal bovine serum (FBS, Gibco-BRL), plus penicillin (100 u/ml), and streptomycin (100 μg/ml, Invitrogen). Cells were cultured at 37°C with 5% CO2. Melan-a2 murine melanocytes were grown in RPMI 1640 medium supplemented with 10% FBS (Gibco-BRL), plus penicillin (100 u/ml), streptomycin (100 μg/ml), 12-0-tetradecanoyl phorbol acetate (200 nM, Sigma), and cholera toxin (200 pM, Sigma). Cells were cultured at 37°C with 10% CO2. Embryonic day 14 (E14) mouse ES cells were either co-cultured with mouse primary embryonic fibroblast feeders or cultured under feeder-free conditions . Cells were maintained in DMEM (GIBCO), supplemented with 15% heat-inactivated fetal bovine serum (GIBCO), plus β-mercaptoethanol (0.055 mM, GIBCO), L-glutamine (2 mM), MEM (0.1 mM nonessential amino acid), penicillin/streptomycin (5,000 units/ml) and leukemia inhibitory factor (1,000 units/ml, Chemicon).
Library construction and PET extraction
Methods for constructing GIS-PET transcriptome libraries and scripts for PET extraction are available for download , and can also be found from our previous publications [20, 27]. Spacers, which interpose PETs in the raw sequences, are defined by the vectors and restriction enzymes used for library constructions. The 5' most spacer is denoted as 5' spacer; the 3' most spacer as 3' spacer; the major internal spacer as spacer1; and the minor internal spacer, which might be generated from incomplete enzymatic manipulation, as spacer2. Libraries SMT001 (B16F1 melanoma library), SMN001 (Melan-a2 melanocyte library) and SME006 (E17.5 embryo library) had the same 5' spacer (GATCGAC), spacer1 (GTCGGATCCGAC), spacer2 (GTCGCGAC), and 3' spacer (GTCGATC), while library MoEScom (E14 embryonic stem cell library) had all spacers of the same sequence 'GTCGGATCCGAC'. The minimum and maximum ditag lengths were 34 and 40, respectively. PET-Tool first identified the spacers and extracted the PET candidates interspersed between the spacers. PET candidates containing more than 8 bp of consecutive A, T, G, or C in either the 5' or 3' tag region were removed, due to the facts that these PET sequences were very likely to be artifacts or contaminants introduced in the wet-lab. N-containing PETs were also removed. The PET extraction process generated a pool of unique PETs (each with a unique sequence) for each library, and each unique PET might have a single or multiple copy number(s), termed PET count. Prior to library comparison, PET counts were normalized to counts per million (cpm) based on the total PET counts of the original libraries, i.e. Every PET count was scaled up by the factor 1,000,000/(total PET count) before the comparison.
Compressed Suffix Arrays (CSA) constructed from the UCSC mouse genome assembly mm5 were used for mapping. Each PET was split into a 5' tag and a 3' tag. From the 5' tag, a set of 9 subsequences were generated by allowing the tag subsequence to start from position 1, 2, or 3, and end at position 17, 18, or 19. The remaining portions formed the 3' subsequences. These subsequences were subjected to mapping against the CSA chromosome constructs. The mapping process identified the chromosome location(s), if present, for each subsequence. Mismatches, deletions, and insertions were not allowed during mapping and the minimum perfect match lengths for the 5' and 3' subsequences were set to 16 and 14 bp, respectively. The 5' hits were then paired with the 3' hits to identify the genomic target locations of the PETs. The criteria for pairing were: both the 5' and 3' mapping locations had to be on the same chromosome, same strand, in 5' followed by 3' order, and within 1 million bp in distance. PETs were then split into PET1 - PET>10 categories based on the number of genomic targets. PETs that could not be mapped under these parameters were assigned to the PET0 category; PETs that mapped to single locations were assigned to the PET1 category; and so on. This study used only PET1 ditags to avoid complication. PET sequence data will be available to the public through T2G website  when the paper is published.
Individual PET-to-exon designation
To assign PET tags to exons, we compared the 5' and 3' mapping locations of each PET to the known gene exons downloaded from the knownGene, refSeq, and MGC tables of the UCSC annotation database (herein, a known gene refers to a gene that matches any of these sources). The PET-to-exon designation is the basis for the "PET-to-transcription unit" annotation. For a PET generated from an mRNA transcribed from a known gene, the 5' tag is expected to map to the first exon and the 3' tag to the last exon of the same gene. However, there were situations where a PET mapped to a novel exon of a known gene or it might map to a known exon but with an offset. To absorb variations in exon boundaries, we extended the starting and ending positions of each exon outwards by 100 bp (Figure 1). A tag, either the 5' or the 3' tag, with a mapping location within such defined exon boundaries was considered a successful match; otherwise, if either end of a PET mapped to the intronic region, it was considered as an intragenic tag. For the terminal exons, we extended the range by 1 Kb, to include plausible novel TSSs or PASs.
If only one side, either the 5' or the 3' tag, matched an exon of a known gene, more stringent criteria were applied to avoid faulty exon annotation. The criteria were: the span between the 5' and 3' tags had to be less than 300,000 bp, and the minimum perfect match lengths for the 5' tag and the 3' tag had to be at least 17 bp and 15 bp, respectively, instead of 16 bp and 14 bp used in default mapping.
We also used a 'SET' system to represent the qualities and natures of PETs that mapped to a particular "transcription unit" ('S', 'E' and 'T' stands for the starting exon, ending exon, and total number of exons, respectively). As an example of a perfect PET-to-transcription unit annotation, 'S1E5T5' indicates that the 5' tag matches to exon1, and the 3' tag matches to exon5 of the same transcription unit that has a total of 5 exons. As an example of an imperfect PET-to-transcription unit annotation, S1E3-4T5 indicates that the 5' tag matches to exon1, and the 3' tag matches to the third intron of the same transcription unit that has a total of 5 exons. The geneID of the transcription unit that owned the PET-associated exon(s) was annotated to the PET with the expression level shown as the PET count. For UCSC database, each geneID has a corresponding geneSymbol (terminology as in UCSC annotation database) and multiple geneIDs may point to the same geneSymbol (N:1 relation).
PET clustering and cluster-to-gene annotation
Here a GIS-PET cluster is defined as a genomic origin, or a gene, that expresses a group of related transcription units. In practice, PET clustering was conducted for two categories separately: one for known gene annotated PETs (gene-based) and the other for un-annotated PETs (coordinate-based, or chromosome location-based). The gene-based clustering was conducted by the following steps: First, all PETs were separated based on the 'SET' designation. PETs with the same starting and ending exons were grouped into the same "sub-cluster" representing a distinguishable "transcription unit", and their counts were summed to represent the expression level of that transcription unit. Second, all the transcripts belonging to the same geneSymbol were further grouped into the same "cluster" with PET counts summed to represent the overall expression level of the gene. Lastly, for a cluster containing multiple geneSymbols, the geneSymbol associated with the majority of PETs was annotated to that cluster and all PET counts were summed to represent the expression level of that gene cluster. Since only known gene PETs can be correlated to the KEGG pathways, there will be no further discussion of PETs clustered by the coordinate-based clustering approach.
Gene level melanoma-melanocyte comparison
B16F1 melanoma and Melan-a2 melanocyte transcriptomes were compared using known genes present in either or both libraries (Figure 2). Results were partitioned into 3 mutually exclusive sets: genes that are exclusive to the B16F1 melanoma library, genes that are shared by both libraries, and genes that are exclusive to the Melan-a2 library. Genes highly expressed in melanoma, but not in melanocytes (or with low expression levels) were listed.
Pathway level melanoma-melanocyte comparison
To facilitate data analysis, we built a local mirror site of KEGG pathway, containing a total of 141 pathways, with a slight modification to reflect our local data status (Figure 3). PET associated genes were correlated to their corresponding KEGG IDs using the file 'keggPathway.txt' available at UCSC database. If the knownGene ID for a PET cluster was not available (e.g. the PETs mapped to a refGene entity) we either converted refGene ID to knownGene ID using 'kgXref.txt' or used the gene symbol to map it to the corresponding KEGG ID. We modified the original pathway images by adding solid squares, each representing a library, to the upper left corner of the gene box to indicate the status of isoform coverage by the libraries. The solid squares were highlighted red, yellow, or blue to indicate that the isoforms all matched, partially matched, or did not match at all, respectively. Links were also created on the solid boxes to allow easy access to additional information. Multiple PET libraries could be displayed in the same page to facilitate side-by-side comparison. Another feature added to the local KEGG pathway database was the expression graph for making cross library comparison over PET counts of all gene isoforms of a particular pathway to enhance visualization (Figure 4).
Testing the feasibility of using PET count to measure gene expression level
The melanin biosynthesis pathway was not listed in the KEGG database, and the analysis was conducted alternatively with the following steps: First, we used UCSC mouse genome database mm5 and the Gene Ontology database  to identify all the melanin biosynthesis related genes. Second, PETs mapped to these genes were identified from all four libraries and their counts were added up for each gene and each library. Then, the PET counts of each gene were compared across all four libraries.
Identification of most significantly altered pathways with hypergeometric distribution
Global pathway comparison was conducted by comparing all pathways using a hypergeometric distribution method with a minor modification to identify the pathways with most significant aberrations. This was conducted by the following steps: Given a gene, its expression ratio r was defined as:
where s0 is a small positive value representing the pseudocount for stabilizing the ratio when the expression level of the gene is low . The s0 was empirically determined to be 5 in our study. With the criterion of 1.5-fold change as the cutoff, we identified upregulated genes (r ≥ 1.5), and downregulated genes (r ≤ 0.67). For each KEGG pathway, we calculated the hypergeometric p-value which indicates the enrichment of regulated genes in the pathway. Pathways with p-values of 0.005 or less were considered to be significantly altered. Manual curation was applied to ensure the quality of pathway analysis.
We used the 'SET' transcription unit definition described above to differentiate transcriptional variants resulted from alternative TSSs or alternative PASs Transcription units sharing the same values of 'S', 'E' and 'T' were considered as common ones. Otherwise they were considered as library specific. The results were split into seven categories.
Partial pathway analysis and manual curation
In general, KEGG pathways are loosely defined and some are partially overlapped with each other; thus, whole pathway comparison can be overgeneralized and overlooks local transcriptional architectures. To compensate this potential problem, some pathways were partially analyzed or manually curated (see Results and Discussion). For example, the galactose-glucose interconversion pathway was extracted from the galactose metabolism pathway to focus on genes directly involved in the galactose and glucose interconversion process. Similarly, the RAS-ERK sub-pathway was extracted from the MAPK pathway and the expression of cyclins and CDKs was obtained from the cell cycle pathway. Manual curation was conducted for the most significantly altered pathways to ensure accuracy.
Results and discussion
The numbers of transcriptome PETs (including the duplicates) totaled 91,977 (equivalent to 45,465 unique PETs) and 68,880 (equivalent to 51,352 unique PETs) for the B16F1 melanoma library and Melan-a2 melanocyte library, respectively (Table 1). After mapping and further characterization, we identified 32,267 PET1 ditags from the melanoma transcriptome. Among these, 29,439 (91.2%) were associated with known genes, and 11,687 (36.2%) of the known gene-associated PET1 ditags were further annotated to KEGG pathways. The melanocyte transcriptome contained 36,623 PET1 ditags, 33,005 (90.1%) were associated with known genes, of which 13,348 (36.4%) were further annotated to KEGG pathways. Overall, the melanocyte library scored the highest success rate (40.4%) for known gene-to-pathway association, followed by the melanoma library (39.7%), the E17.5 day old embryo library (37.8%), and the E14 stem cell library (32.9%). The distinct difference in annotatable rate between the melanocytic libraries and the embryonic libraries (especially the E14 stem cell) suggests that certain developmental pathways are presently uncharacterized and not available in the KEGG databases.
Melanin de novo biosynthesis genes are highly expressed in the cells of melanocyte origin, but not in the embryonic cells
The melanogenic potential is genetically endowed by two groups of genes encoding enzymes of Tyrosinase family and Pmel/Si family , which work in the up- and down-stream of the melanin biosynthesis pathway respectively. Members of the Tyrosinase family include tyrosinase precursor (encoded by Tyr gene), Dopachrome tautomerase precursor (Dct, or Tyrp2 gene), D-dopachrome tautomerase (Ddt gene), and DHICA oxidase precursor (Tyrp1 gene). The silver locus protein (Si) is the murine homolog of human Pmel 17 protein.
As expected, melanin biosynthesis genes were predominantly expressed in the melanocytic cells including the B16F1 melanoma cells and the Melan-a2 melanocytes, but not, or at extremely low levels, in the embryonic cells including E17.5 embryo cells and E14 embryonic stem cells (Table 2). Moreover, comparisons between melanoma cells and melanocytes revealed a pathway-wide, consistent transcriptional reduction of the major melanin biosynthesis genes in melanoma (p = 0.0018) especially for genes expressed at high level in melanocytic cells, indicating a coordinated transcriptional control for genes of the same metabolic pathway. This result thus suggests the feasibility of using PET counts for the pathway-wide quantification of gene expression levels.
The most significantly upregulated pathways are diversely involved in various cellular activities
A total of 7 pathways were found to be significantly upregulated (p < 0.005) in melanoma cells, and these were either related to purine, amino acid, or lipid biosynthesis, or the degradation of xenobiotic compounds (Table 3). High activation of the purine biosynthesis pathway occurred in most of the enzymes involved in ATP or GTP synthesis, starting from the biosynthesis of ribose 5-phosphate all the way through PRPP, inosinate (IMP), xanthylate, to the formation of ATP and GTP. The aminophosphonate metabolic pathway upregulation might lead to an increase in phospholipid biosynthesis. Upregulation of nitrobenzene degradation and bisphenol A degradation pathways would help melanoma cells detoxify xenobiotic compounds, in which cytochrome P450 plays an important role. Transcription of P450 per se was increased from an undetectable level in melanocytes to 44 cpm in melanoma cells. Biosynthesis of the amino acid tyrosine was activated in melanoma cells as suggested by the transcriptional upregulation of tyrosine biosynthesis genes. However, the utilization of tyrosine residues in melanoma cells is unclear because the transcriptional levels of the enzymes involved in consuming tyrosine for melanin synthesis in melanoma were all lower than in melanocytes (4.4, 1.6, and 2.2 fold differences for Tyr, Tyrp1, and Dct, respectively) and enzymes involved in downstream tyrosine utilization were mostly lower in melanoma cells. Lastly, transcriptional activation was found in most of the enzymes of the galactose pathway, especially those involved in the galactose-glucose interconversion process (Table 4) including galactosekinase 1, UDP-galactose-4-epimerase, and UDP-glucose pyrophosphorylase 2, suggesting that melanoma cells are more active than melanocytes in using galactose not only to use it as the carbon and energy sources, but also for detoxification because galactose is highly toxic if accumulated in the cell.
Glycolysis is the biological process that converts glucose to pyruvate with ATP production. The process can be divided into upstream and downstream processes. The upstream process converts one molecule of glucose into one molecule of dihydroxyacetone phosphate (which is subsequently converted into glyceraldehyde 3-P) and one molecule of glyceraldehyde 3-P. The downstream process converts two glyceraldehyde 3-P molecules into two pyruvate molecules.
In melanoma cells, although the overall glycolysis pathway is not upregulated, most of the enzymes involved in the upstream reaction were upregulated, especially phosphoglucose isomerase (255:450 in cpm), which interconverts glucose 6-P and fructose 6-P, and aldolase (1263:1784 in cpm), which interconverts fructose 1,6-bisphosphate and glyceraldehydes 3-P/dihydroxyacetone phosphate.
The PI3K/Akt lipid kinase signaling pathway, which is involved in diverse cellular activities including glucose metabolism, was activated in melanoma cells. Expression levels of PI3K and Akt were 11 cpm and 176 cpm, respectively, in melanoma cells; compared with 0 cpm and 90 cpm in melanocytes.
Most of the significantly downregulated pathways reside in mitochondria and are related to energy metabolisms through the electron transport chain
Eight pathways were found significantly downregulated (p < 0.005) in melanoma cells (Table 3). Three of them were excluded by manual curation due to the following reasons: 1) The Reductive carboxylate cycle is actually a reverse TCA cycle, and TCA cycle was already included. 2) The C5-branched dibasic acid metabolism pathway comprises only two genes, IlvB and Sucla2; and Sucla2 encodes a succinate-CoA ligase, which is also a component of the TCA cycle. 3) Lastly, the pyrimidine biosynthesis pathway consists of 72 gene isoforms listed in the KEGG database, of which 12 were shown to be downregulated and another 12 were shown to be upregulated (as defined by r ≤ 0.67, see Methods section), making it difficult to draw a conclusion. Thus, a total of 5 pathways were characterized as the most significantly downregulated pathways.
The top 4 of these pathways were oxidative phosphorylation (biosynthesis of ETC components), ATP synthesis (biosynthesis of ATPase subunits), TCA cycle, and pyruvate metabolism (Figure 4), all of which take place in the mitochondria and are directly or indirectly involved in ATP production through ETC. Cytochrome C (a component of oxidative phosphorylation) decreased 2.6 folds. Two of the most striking observations of the pyruvate pathway were: 1) Universal downregulation of all enzymes that convert pyruvate to Acetyl-CoA, including a 5-fold decrease for pyruvate dehydrogenase (Pdhb), a 6.8-fold decrease for dihydrolipoamide dehydrogenase (Dld), and a 2.7-fold decrease for dihydrolipoamide S-acetyltransferase (Dlat). 2) A10.5-fold increase of lactate dehydrogenase 1, A chain (Ldh1), which interconverts pyruvate and D-lactate. Thus, melanoma cells tend to consume pyruvate through anaerobic fermentation. Since Acetyl-CoA is the intermediate metabolite that enters the TCA cycle for ATP production through ETC, downregulation of Acetyl-CoA production well correlates with the downregulation of TCA cycle, oxidative phosphorylation, and ATP synthesis pathways.
Glutathione molecules are the major group of non-protein thiols in the cell. They mainly act as antioxidants (e.g. Glutathione peroxidases), reducing agents (e.g. Glutathione dehydroascobate reductase), and detoxification agents (e.g. Glutathione-dependent S-transferase), and form a redox buffer in the cell through the interconversion between reduced monomers and oxidized dimers mediated by di-sulfide bond breakage or formation, respectively. Downregulation of glutathione metabolism was observed mainly in two routes: 1) the interconversion between the reduced and the oxidized forms of glutathione, and 2) the transition from the reduced glutathione to R-S-glutathione (Figure 5). In these regions, 87.5% (14/16) of the gene isoforms showed reduced expressions. Downregulation of glutathione metabolism might be related to the downregulation of the above-mentioned mitochondrial pathways. Reduced TCA cycle and ETC activities implied lower reactive oxygen species (ROS) production. Thus, the synthesis of glutathione pathway enzymes was reduced accordingly. Using proteomic and SAGE profiling de Souza et al. also observed the same trend in melanoma cell lines Tm1 and Tm5, when compared with the melan-a melanocyte from which the Tm1 and Tm5 were derived .
Upregulation of RAS-MAPK pathway genes, and c-Myc in B16F1 melanoma cells
Activation of the mitogen activated protein kinase (MAPK) pathway occurs in most tumors and is a common event in uveal melanomas, although it rarely occurs through mutation of RAS or BRAF [1, 33, 34]. The RAS-MAPK cascade activates c-fos, c-Myc and stress-activated protein kinases (MSKs), which in turn phosphorylate histone H3, leading to chromatin remodeling and activation of specific genes .
We found transcriptional upregulation in melanoma cells across major RAS-MAPK (ERK1) pathway genes including Ras, Raf, Mek, and Erk, together with a significant isoform switch in Ras transcripts (Table 5). Within Ras isoforms, there was a 4-fold decrease for H-ras1, a 3-fold increase for R-ras, and a plausible induction of K-ras in melanoma cells (0 cpm in melanocytes, compared with 11 cpm in melanoma cells). Recent reports indicate that expression of the K-ras oncogene accelerates tumorigenesis in the context of APC deficiency . In this study, PTEN, APC, and BRAF (B-type RAF kinase) transcripts were not detected in both cell types.
The expression level of c-Myc was 33 cpm (with two isoforms) in melanoma cells, as compared with an undetectable level in melanocytes. c-MYC protein was shown to play a crucial role in human carcinogenesis, and β-catenin (the effector protein of the Wnt signaling) was able to activate c-Myc expression  in the presence of TCF/LEF. The enhanced expression of c-Myc contributes to most aspects of tumor cell biology, including cell cycle progression, cell differentiation, apoptosis, metastasis and angiogenesis [7, 38]. Activated c-Myc  or Ras  can induce chromosome breakage and increase the frequency of gene amplification. Crosstalk between c-MYC and other pathways, including p53 and Wnt/β-catenin pathways has been shown to exert profound effects on many cellular aspects.
Upregulation of Trp53, and cell cycle progression gene expressions
p53 plays an important role in suppressing tumor development and p53 mutations have been found in 50% of human cancer patients . The mouse p53-encoding gene Trp53 of B16F1 was previously characterized as a wild-type by genetic studies  and the p53 protein, although expressed at low level, was localized to the nucleus and thus expected to be functionally normal. However, we detected a level of 262 cpm for Trp53 mRNA in B16F1 melanoma cells, in contrast to an undetectable level in Melan-a2 melanocytes (Figure 6). The upward transcriptional regulation of p53 did not seem to be compatible with its (low) protein level and might imply a translational control or protein degradation of p53 in melanoma cells. Genetic studies also identified a deletion spanning across the overlapping loci encoding p16INK4a and p19ARF proteins (mouse Cdkn2a of Ink4a-d, shown on the left-hand side of Figure 6) [13, 41]. The deletion is supposed to derepress the cell cycle arrest by INK4a protein, which would otherwise binds to CDK4,6 and causes cell cycle arrest at G1 phase. In line with the report, the Cdkn2a (and Arf) transcript was not detected in melanoma cells. ARF protein counteracts the degradation of p53 by MDM2; thus, deletion in the Arf gene would reduce the protein level of p53. It is likely that the transcription activation of p53 in melanoma cells was due to activation by c-MYC. The presence of the E-box in the p53 promoter directly places p53 under the transcriptional control by c-MYC, and it is not surprising to see co-activation of p53 and c-MYC [42, 43]. Elevation of p53 pathway expression was also shown in cMYC induced DNA damage and RAS activation .
Besides p53, the tumor suppressor genes Atm and Cdkn1a (p21 gene) were expressed higher in melanoma cells than melanocytes (65:0 and 22:0 in cpm, respectively). It was reported that the expression levels of c-MYC, proliferating cell nuclear antigen (PCNA), and p53 were all higher in metastasizing colorectal cancer than non-metastasizing tumors as detected by immunohistochemistry .
Cell cycle progression is tightly regulated by two types of controls: a rhythmic expression of cyclins in conjunction with their interactions with their kinase partners, and a supervisory control through diversified checkpoint monitoring mechanisms . PCNA, a nuclear protein used as an indicator of cell proliferation, increased from 104 cpm in melanocyte to 1311 cpm in melanoma (12.6 fold), implying aggressive growth of melanoma cells. In general, compared to melanocytes, the transcriptional levels of cyclins and cyclin-dependent kinases are all elevated in melanoma cells (Figure 6).
Perturbations in apoptosis pathway: elevation of caspase 8 transcription and E2f1-to-E2f4 switch
Two alterations were apparent in melanoma apoptosis pathway: elevation of caspase 8 transcription and an E2f1-to-E2f4 gene isoform switch.
Expression of caspase 8 was significantly increased (0:154 cpm) in melanoma cells. Both Bad and Bax expression levels were increased slightly and Bad showed isoform induction, suggesting that there might be apoptotic pressures, causing the pathway to be upregulated at some points. However, like the p53 pathway, the apoptosis pathway seemed to be disoriented and deregulated.
We found an E2f1-to-E2f4 switch in melanoma cells, wherein p73 transcript was not present. E2Fs are known to be crucial regulators of a variety of cellular events including cell cycle progression, DNA replication, checkpoint control, apoptosis, and DNA repair , and E2F1 is crucial for E2F-dependent apoptosis [47, 48]. In general, E2Fs can be divided into activators (E2F1-3) and repressors (E2F4 and E2F5). However, it is technically possible for the repressors to activate certain genes. E2F1 induces the transcription of p73 which in turn activates the apoptosis pathway [40, 49]. The capability of p73 to induce apoptosis in TP53 -/- cells is a p53-independent tumor control mechanism that runs in parallel with p53-dependent apoptosis. There were six E2f gene isoforms (E2f1-E2f6) listed in KEGG database, among which melanocytes expressed E2f1 (60 cpm) and E2f5 (15 cpm), while melanoma cells expressed E2f4 (11 cpm) and E2f5 (11 cpm). It seems likely that melanoma cells adopt the E2f1-to-E2f4 switch as a strategy to avoid E2F1-p73-dependent apoptosis. As E2Fs regulate a broad spectrum of cellular activities, it remains to be learned how such a switch in E2f isoforms affects overall cancer cell physiology. It is possible that melanoma cells may still express E2f1 at a redefined basal level below our detection limit to sustain the transcription of certain genes.
Cell adhesion and metastasis related genes were expressed as diverse isoforms in melanoma cells
Recently β-catenin has drawn a great attention due to its dual role in signal transduction and cell adhesion. It is not only a transcription factor that activates genes such as c-Myc, but also a structural adaptor protein that bridges extracellular cadherins through α-catenin to the intracellular actin cytoskeleton network, which is crucial for cell-cell adhesion and migration .
Metastases are responsible for most cancer deaths and the involvement of adhesion proteins in metastasis has been well documented [1, 8]. Since B16F1 is a metastatic melanoma cell line, it is of particular interest to find out what adhesion proteins are expressed in melanoma cells. In both normal melanocytes and melanoma cells, transcripts of extracellular adhesion proteins such as nectin (weak cell-cell glue protein) and cadherin (strong cell-cell glue protein) were low or not detected (Table 6), suggesting that minimal cell-cell contact through cadherin was a common scheme for both cell lines. However, it could be an artifact resulted from the process of cell culture. Like that of β-catenin, integrin expression was very diverse in melanoma cells. The two expressed integrin genes included: full-length (exon 1–16) Itgb1 (expressed in both cell types, but melanoma cells had one extra isoform with the PAS located in exon 10); and Itgb5 (specifically expressed 3 different types of isoforms – with different TSSs – in melanocytes). An 8-fold increase for CD44 isoforms (S1E14T14, accompanied with S1E12T14 and S1E4T14 that were expressed at lower level) was found in melanoma cells. Since CD44 is able to induce integrin-mediated adhesion of colon cancer cell lines to endothelial cells , the process by which CD44 interacts with such diversified integrin isoforms is an interesting issue to be addressed. Moreover, CD44 was identified as a marker of cancer progression and its variants play a role in metastasis . There were 4.6× and 5.8× increases for Actb and Actg1 isoforms of the cytoskeleton protein actin, respectively, in melanoma cells as compared with melanocytes. The increase in actin expression may not be relevant to metastasis; it may contribute to the identity of melanoma skin cancers as solid tumors instead.
Besides the transcript variants resulted from alternative splicing, transcriptions using alternative TSSs or PASs generate different types of transcripts with variations in the 5'UTRs or 3'UTRs, which are more likely to be involved in regulation of gene expression compared with other (internal) exons. One of the unique advantages of PET approach is its capability to precisely map the 5' and 3' boundaries specified by alternative TSSs and alternative PASs, respectively. It was reported that a total of 5,401 genes were found to be alternatively spliced in Melan-c and B16-F10Y melanoma cell lines . Melan-a2 melanocytes and B16F1 melanoma cells are similar to Melan-c melanocyte and B16-F10Y melanoma cells, respectively. Among the total of 5,606 genes identified from melanoma and melanocyte cells, 1,289 genes (23.0%) exhibited alternative TSSs/PASs, 2,714 genes (48.4%) showed library-specific expressions, and 1,603 genes (28.6%) expressed only common transcripts (Table 7). In theory, the percentage of genes using alternative TSSs/PASs is more likely to increase as the library size increases. Transcriptional control with alternative TSSs or PASs seems to be a common mechanism for melanocytic cells.
Transcription of solute carriers (SLCs)
To gain insight into perturbations in mitochondria, we analyzed the expression of a group of membrane transporter proteins called solute carriers (SLCs) . A total of 67 SLCs were detected in melanoma and/or melanocyte transcriptomes. To increase the accuracy of the data, we excluded the PETs of less than 20 cpm because these were single count PETs before normalization, resulting in 44 SLCs of reasonable confidence (Table 8). Four discoveries were made from this dataset: i) SLCs heavily expressed in melanocytes remained heavily expressed in melanoma, especially Slc25a5, Slc3a2, and Slc25a3. ii) Among these highly expressed SLCs, Slc25a5 (an ATP/ADP transporter) increased by 3.2 folds and was the most noticeable perturbation in SLC expression. iii) SLCs specific to melanoma cells or melanocytes were expressed at a much lower level, normally less than 100 cpm, except Slc6a15 (amino acid and osmolyte transporter) which had a cpm of 109. iv) As shown by the cell type specific SLCs, melanoma cells seemed to be more active in the transportation of amino acids (e.g. Slc6a15, Slc25a13, and Slc7a7), fatty acids (e.g. Slc27a4), UDP-galactose (e.g. Slc35a2, Slc35a4), Mg++ ion (e.g. Slc41a3), and citrate/malate (e.g. Slc25a10 ). The melanoma-specific SLC expression levels and Slc25a5 activation level correlated well with the activations of the purine, galactose, and amino acid related metabolic pathways. When these pathways were activated, production of the proteins involved in the transportation of their substrate and/or products was also increased accordingly.
This study aimed to reveal global pathway aberrations in melanoma cells using the robust GIS-PET technology in conjunction with KEGG pathway database and hypergeometric distribution analysis. Surprisingly, all the most significantly altered pathways, including 7 upregulated and 5 downregulated pathways, are metabolic pathways. The most significantly upregulated melanoma pathways are very diverse as they are involved in a broad spectrum of cellular activities including purine and amino acid biosyntheses, galactose utilization, and detoxification of various harmful compounds. On the other hand, the most significantly downregulated pathways are tightly correlated, making the conclusion highly reliable and trustworthy. Here, for the first time in melanoma, we provide compelling evidence to show that cancer cells tend to avoid using the most efficient route of ATP production through electron transport chain, which is located in mitochondrial inner membrane and which uses oxygen as the electron receptor.
This notion is mainly based on the observation that mitochondria-harbored metabolic pathways are severely downregulated. In eukaryotic cells, the top 4 of the most significantly downregulated melanoma pathways constitute an important catabolic flow for intermediate metabolite and energy productions (from pyruvate metabolism, through TCA cycle and oxidative phosphorylation, to ATP synthesis). To further avoid using this route, melanoma cells tend to consume pyruvate molecules to produce D-lactate instead of Acetyl-CoA (a substrate for TCA cycle). Moreover, in parallel with the metabolic alterations, mitochondrial permeability and transportation system are also redefined. Among the SLCs, we detected upregulation of citrate/malate exchanger Slc25a10. In exchange for malate from cytosol, the citrate/malate exchanger exports citrate from mitochondria into cytosol for lipid biosynthesis . Since citrate is an intermediate metabolite of TCA cycle for the generations of NADH and FADH2, which in turn are passed on to the respiratory chain for ATP production, elevation of the citrate/malate exchanger is an additional step to reduce the capacity for ATP production through the ETC.
Our data also indicated that melanoma cells increased the consumption of glucose and galactose for ATP synthesis and intermediate metabolite production. In melanoma cells, galactose pathway and the galactose-glucose conversion pathway were both transcriptionally upregulated. We suspect that these upregulations aimed not only to support cancer cell proliferation, but also to reduce the intracellular concentration of galactose, which is a potent toxin for the cell. Running side by side with the upregulated detoxification pathways, transcriptional upregulation of the galactose-glucose interconversion pathway would neutralize the galactose toxicity, which can be critical in the solid tumor environment where circulation is much more limited than normal cells. Notice that the expression of Slc35a2, an UDP-galactose transporter, was also upregulated by 3.8 folds in melanoma cells. The increased consumption of carbohydrates, intermediate metabolites and other nutrients from the circulation system for tumor growth eventually leads to cancer cachexia .
It is interesting to compare our results with that of Vahsen et al . AIF (apoptosis inducing factor) is a protein that, in response to apoptosis induction, translocates from mitochondria to the nucleus to exert its chromatinolytic activity. They described that human or mouse cells lacking AIF would exhibit high lactate production and enhanced dependency on glycolytic ATP production due to severe reduction of ETC complex I activity. Moreover, mice with reduced AIF expression demonstrated a reduced oxidative phosphorylation. Their results suggested a role of AIF in the biogenesis and/or maintenance of complex I of the electron transport chain. In our investigation, AIF transcript was not detected in both melanoma and melanocyte cells and thus did not contribute to the physiological differences between melanoma cells and melanocytes. However, the expression levels of the ETC pathway as well as the above-mentioned metabolic pathways were all lower in melanoma cells. Thus, the same phenomena were observed with different approaches.
Then, how is the slowdown of mitochondrial activities related to cancer cell survival? Due to the critical role of mitochondria in apoptosis  and the importance of angiogenesis in cancer neoplasia, we argue that downregulation of mitochondrial pathways leading to the reduction of ETC usage by melanoma cells is actually a "one stone for two birds" strategy, aiming to downgrade the role of mitochondria in apoptosis and to reduce the dependency of the cell on angiogenesis for oxygen supply (and toxic material removal), which is very limited during the early stage of angiogenesis. Thus, these issues are tightly correlated and melanoma cells sacrifice the most efficient way of ATP production in exchange, at least, for a reduced threat from apoptosis and a reduced dependency on angiogenesis. This notion further emphasizes the importance of mitochondria for normal cellular functions and deregulated mitochondria would favor the survival of tumor cells. Notice that enhanced detoxification capability would also reduce the dependency on angiogenesis for the removal of toxic compounds.
It is interesting to learn how melanoma cells can still manage to grow vigorously (as indicated by the 12.6-fold increase of PCNA expression level) despite the surveillance of cell cycle progression checkpoints and apoptotic pathways in the context of such drastic alterations in multiple pathways. Based on the coexistence of the transcriptional upregulation of Trp53 and Ink4a/Arf deletion in the p53 pathway, the deregulated cell cycle progression, and the scattered pattern of alterations in the apoptosis pathways, etc., both tumor suppressor mechanism and apoptosis pathway seemed to be shattered into discrete pieces in which the coordination between the components no longer existed. How these pathways are deregulated and how changes at the p53 transcription level are translated to changes in the protein and protein phosphorylation, which is required for p53 activation, remains to be understood.
Based on the notion that cancers generally develop from multiple mutations in diverse genes, we would expect multiple pathways to be altered, as has been shown in our data. Due to the extensiveness of the renovation of melanoma pathways, the selectivity for certain anabolic, catabolic, or signal transduction pathways to be upregulated or downregulated for melanoma cell survival seem to be taking place through a series of micro-evolution process involving numerous testing of mutations and selections in the context of carcinogenesis environment inside the tumor mass.
Although pathway studies reflect the combinatorial outcomes of functionally related genes and are supposed to be more reliable than studies of individual genes or gene sets, the results, however, were generated only from B16F1 melanoma cell line. The generality need to be confirmed with other cancer cell lines or cancer tissue samples. By such additional works, we should also be able to further clarify how many of these changes were resulted from adaptation of the cells to in vitro culture conditions.
Moreover, the hypergeometric distribution approach can be made even more powerful through improving the resolution by looking into the sub-pathways for each pathway. As described in the study of the pyruvate metabolic pathway, a sub-pathway may be favored against the others. Under this situation, the resolution of hypergeometric distribution would be compromised. To address this issue, one would have to dissect each pathway into distinct sub-pathways, which requires laborious functional studies on each pathway and is a component of our future work.
In summary, by using the GIS-PET technology in combination with KEGG database and hypergeometric distribution analysis, we demonstrate the most significantly upregulated and downregulated melanoma pathways and reemphasize the importance of mitochondrial deregulation for cancer survival. Enzymes of the altered pathways, such as the galactose-glucose interconversion pathway, signaling pathway components that have been altered, and the upregulated transporter proteins in melanoma cells can be tested as drug targets for cancer therapy. We believe this approach, which can be readily correlated with other PET approaches such as ChIP-PET, will significantly facilitate our understanding of gene expression and regulation at the pathway level.
Compressed suffix array
Electron transport chain, or respiratory chain
Kyoto Encyclopedia of Genes and Genome
Polymerase chain reaction
Paired-End diTag, indicating either the technology or the PET sequence generated from the technology
PET technology or PET ditag (sequence)
Reactive oxygen species
cycle Tricarboxylic acid cycle, or citric acid cycle, or Krebs cycle
Transcription factor binding site
Transcription start site
Hanahan D, Weinberg RA: The hallmarks of cancer. Cell. 2000, 100: 57-70. 10.1016/S0092-8674(00)81683-9.
Hahn WC, Weinberg RA: Modelling the molecular circuitry of cancer. Nat Rev Cancer. 2002, 2: 331-341. 10.1038/nrc795.
Hussein MR: Genetic pathways to melanoma tumorigenesis. J Clin Pathol. 2004, 57: 797-801. 10.1136/jcp.2003.015800.
Feinberg AP, Ohlsson R, Henikoff S: The epigenetic progenitor origin of human cancer. Nat Rev Genet. 2006, 7: 21-33. 10.1038/nrg1748.
Felsher DW, Bishop JM: Transient excess of MYC activity can elicit genomic instability and tumorigenesis. Proc Natl Acad Sci U S A. 1999, 96: 3940-3944. 10.1073/pnas.96.7.3940.
Yang JL, Ow KT, Russell PJ, Ham JM, Crowe PJ: Higher expression of oncoproteins c-myc, c-erb B-2/neu, PCNA, and p53 in metastasizing colorectal cancer than in nonmetastasizing tumors. Ann Surg Oncol. 1996, 3: 574-579. 10.1007/BF02306092.
Dang CV: c-Myc target genes involved in cell growth, apoptosis, and metabolism. Mol Cell Biol. 1999, 19: 1-11.
Chambers AF, Groom AC, MacDonald IC: Dissemination and growth of cancer cells in metastatic sites. Nat Rev Cancer. 2002, 2: 563-572. 10.1038/nrc865.
Nelson WJ, Nusse R: Convergence of Wnt, beta-catenin, and cadherin pathways. Science. 2004, 303: 1483-1487. 10.1126/science.1094291.
La Porta CA: Perspectives in melanoma treatment with signal transduction. Curr Med Chem Anticancer Agents. 2002, 2: 371-385. 10.2174/1568011024606398.
Haluska FG, Tsao H, Wu H, Haluska FS, Lazar A, Goel V: Genetic alterations in signaling pathways in melanoma. Clin Cancer Res. 2006, 12: 2301s-2307s. 10.1158/1078-0432.CCR-05-2518.
Kaul R, Mukherjee S, Ahmed F, Bhat MK, Chhipa R, Galande S, Chattopadhyay S: Direct interaction with and activation of p53 by SMAR1 retards cell-cycle progression at G2/M phase and delays tumor growth in mice. Int J Cancer. 2003, 103: 606-615. 10.1002/ijc.10881.
Melnikova VO, Bolshakov SV, Walker C, Ananthaswamy HN: Genomic alterations in spontaneous and carcinogen-induced murine melanoma cell lines. Oncogene. 2004, 23: 2347-2356. 10.1038/sj.onc.1207405.
Schulze A, Downward J: Navigating gene expression using microarrays--a technology review. Nat Cell Biol. 2001, 3: E190-5. 10.1038/35087138.
Chung HJ, Kim M, Park CH, Kim J, Kim JH: ArrayXPath: mapping and visualizing microarray gene-expression data with integrated biological pathway resources using Scalable Vector Graphics. Nucleic Acids Res. 2004, 32: W460-4. 10.1093/nar/gkh476.
Velculescu VE, Zhang L, Vogelstein B, Kinzler KW: Serial analysis of gene expression. Science. 1995, 270: 484-487. 10.1126/science.270.5235.484.
Saha S, Sparks AB, Rago C, Akmaev V, Wang CJ, Vogelstein B, Kinzler KW, Velculescu VE: Using the transcriptome to annotate the genome. Nat Biotechnol. 2002, 20: 508-512. 10.1038/nbt0502-508.
Boon K, Osorio EC, Greenhut SF, Schaefer CF, Shoemaker J, Polyak K, Morin PJ, Buetow KH, Strausberg RL, De Souza SJ, Riggins GJ: An anatomy of normal and malignant gene expression. Proc Natl Acad Sci U S A. 2002, 99: 11287-11292. 10.1073/pnas.152324199.
Tuteja R, Tuteja N: Serial Analysis of Gene Expression: Applications in Human Studies. J Biomed Biotechnol. 2004, 2004: 113-120. 10.1155/S1110724304308119.
Ng P, Wei CL, Sung WK, Chiu KP, Lipovich L, Ang CC, Gupta S, Shahab A, Ridwan A, Wong CH, Liu ET, Ruan Y: Gene identification signature (GIS) analysis for transcriptome characterization and genome annotation. Nat Methods. 2005, 2: 105-111. 10.1038/nmeth733.
Carninci P, Kasukawa T, Katayama S, Gough J, Frith MC, Maeda N, Oyama R, Ravasi T, Lenhard B, Wells C, Kodzius R, Shimokawa K, Bajic VB, Brenner SE, Batalov S, Forrest AR, Zavolan M, Davis MJ, Wilming LG, Aidinis V, Allen JE, Ambesi-Impiombato A, Apweiler R, Aturaliya RN, Bailey TL, Bansal M, Baxter L, Beisel KW, Bersano T, Bono H, Chalk AM, Chiu KP, Choudhary V, Christoffels A, Clutterbuck DR, Crowe ML, Dalla E, Dalrymple BP, de Bono B, Della Gatta G, di Bernardo D, Down T, Engstrom P, Fagiolini M, Faulkner G, Fletcher CF, Fukushima T, Furuno M, Futaki S, Gariboldi M, Georgii-Hemming P, Gingeras TR, Gojobori T, Green RE, Gustincich S, Harbers M, Hayashi Y, Hensch TK, Hirokawa N, Hill D, Huminiecki L, Iacono M, Ikeo K, Iwama A, Ishikawa T, Jakt M, Kanapin A, Katoh M, Kawasawa Y, Kelso J, Kitamura H, Kitano H, Kollias G, Krishnan SP, Kruger A, Kummerfeld SK, Kurochkin IV, Lareau LF, Lazarevic D, Lipovich L, Liu J, Liuni S, McWilliam S, Madan Babu M, Madera M, Marchionni L, Matsuda H, Matsuzawa S, Miki H, Mignone F, Miyake S, Morris K, Mottagui-Tabar S, Mulder N, Nakano N, Nakauchi H, Ng P, Nilsson R, Nishiguchi S, Nishikawa S, Nori F, Ohara O, Okazaki Y, Orlando V, Pang KC, Pavan WJ, Pavesi G, Pesole G, Petrovsky N, Piazza S, Reed J, Reid JF, Ring BZ, Ringwald M, Rost B, Ruan Y, Salzberg SL, Sandelin A, Schneider C, Schonbach C, Sekiguchi K, Semple CA, Seno S, Sessa L, Sheng Y, Shibata Y, Shimada H, Shimada K, Silva D, Sinclair B, Sperling S, Stupka E, Sugiura K, Sultana R, Takenaka Y, Taki K, Tammoja K, Tan SL, Tang S, Taylor MS, Tegner J, Teichmann SA, Ueda HR, van Nimwegen E, Verardo R, Wei CL, Yagi K, Yamanishi H, Zabarovsky E, Zhu S, Zimmer A, Hide W, Bult C, Grimmond SM, Teasdale RD, Liu ET, Brusic V, Quackenbush J, Wahlestedt C, Mattick JS, Hume DA, Kai C, Sasaki D, Tomaru Y, Fukuda S, Kanamori-Katayama M, Suzuki M, Aoki J, Arakawa T, Iida J, Imamura K, Itoh M, Kato T, Kawaji H, Kawagashira N, Kawashima T, Kojima M, Kondo S, Konno H, Nakano K, Ninomiya N, Nishio T, Okada M, Plessy C, Shibata K, Shiraki T, Suzuki S, Tagami M, Waki K, Watahiki A, Okamura-Oho Y, Suzuki H, Kawai J, Hayashizaki Y: The transcriptional landscape of the mammalian genome. Science. 2005, 309: 1559-1563. 10.1126/science.1112014.
Wei CL, Wu Q, Vega VB, Chiu KP, Ng P, Zhang T, Shahab A, Yong HC, Fu Y, Weng Z, Liu J, Zhao XD, Chew JL, Lee YL, Kuznetsov VA, Sung WK, Miller LD, Lim B, Liu ET, Yu Q, Ng HH, Ruan Y: A global map of p53 transcription-factor binding sites in the human genome. Cell. 2006, 124: 207-219. 10.1016/j.cell.2005.10.043.
Loh YH, Wu Q, Chew JL, Vega VB, Zhang W, Chen X, Bourque G, George J, Leong B, Liu J, Wong KY, Sung KW, Lee CW, Zhao XD, Chiu KP, Lipovich L, Kuznetsov VA, Robson P, Stanton LW, Wei CL, Ruan Y, Lim B, Ng HH: The Oct4 and Nanog transcription network regulates pluripotency in mouse embryonic stem cells. Nat Genet. 2006, 38: 431-440. 10.1038/ng1760.
Matesic LE, Yip R, Reuss AE, Swing DA, O'Sullivan TN, Fletcher CF, Copeland NG, Jenkins NA: Mutations in Mlph, encoding a member of the Rab effector family, cause the melanosome transport defects observed in leaden mice. Proc Natl Acad Sci U S A. 2001, 98: 10238-10243. 10.1073/pnas.181336698.
Watahiki A, Waki K, Hayatsu N, Shiraki T, Kondo S, Nakamura M, Sasaki D, Arakawa T, Kawai J, Harbers M, Hayashizaki Y, Carninci P: Libraries enriched for alternatively spliced exons reveal splicing patterns in melanocytes and melanomas. Nat Methods. 2004, 1: 233-239. 10.1038/nmeth719.
PET-TOOL Website. [http://www.gis.a-star.edu.sg/PET_Tool]
Chiu KP, Wong CH, Chen Q, Ariyaratne P, Ooi HS, Wei CL, Sung WK, Ruan Y: PET-Tool: a software suite for comprehensive processing and managing of Paired-End diTag (PET) sequence data. BMC Bioinformatics. 2006, 7: 390-10.1186/1471-2105-7-390.
T2G Website. [http://t2g.bii.a-star.edu.sg]
Ashburner M, Ball CA, Blake JA, Botstein D, Butler H, Cherry JM, Davis AP, Dolinski K, Dwight SS, Eppig JT, Harris MA, Hill DP, Issel-Tarver L, Kasarskis A, Lewis S, Matese JC, Richardson JE, Ringwald M, Rubin GM, Sherlock G: Gene ontology: tool for the unification of biology. The Gene Ontology Consortium. Nat Genet. 2000, 25: 25-29. 10.1038/75556.
Boer JM, Huber WK, Sultmann H, Wilmer F, von Heydebreck A, Haas S, Korn B, Gunawan B, Vente A, Fuzesi L, Vingron M, Poustka A: Identification and classification of differentially expressed genes in renal cell carcinoma by expression profiling on a global human 31,500-element cDNA array. Genome Res. 2001, 11: 1861-1870.
Lee ZH, Hou L, Moellmann G, Kuklinska E, Antol K, Fraser M, Halaban R, Kwon BS: Characterization and subcellular localization of human Pmel 17/silver, a 110-kDa (pre)melanosomal membrane protein associated with 5,6,-dihydroxyindole-2-carboxylic acid (DHICA) converting activity. J Invest Dermatol. 1996, 106: 605-610. 10.1111/1523-1747.ep12345163.
de Souza GA, Godoy LM, Teixeira VR, Otake AH, Sabino A, Rosa JC, Dinarte AR, Pinheiro DG, Silva WA, Eberlin MN, Chammas R, Greene LJ: Proteomic and SAGE profiling of murine melanoma progression indicates the reduction of proteins responsible for ROS degradation. Proteomics. 2006, 6: 1460-1470. 10.1002/pmic.200500243.
Zuidervaart W, van Nieuwpoort F, Stark M, Dijkman R, Packer L, Borgstein AM, Pavey S, van der Velden P, Out C, Jager MJ, Hayward NK, Gruis NA: Activation of the MAPK pathway is a common event in uveal melanomas although it rarely occurs through mutation of BRAF or RAS. Br J Cancer. 2005, 92: 2032-2038. 10.1038/sj.bjc.6602598.
Xing M: BRAF mutation in thyroid cancer. Endocr Relat Cancer. 2005, 12: 245-262. 10.1677/erc.1.0978.
Dunn KL, Espino PS, Drobic B, He S, Davie JR: The Ras-MAPK signal transduction pathway, cancer and chromatin remodeling. Biochem Cell Biol. 2005, 83: 1-14. 10.1139/o04-121.
Sansom OJ, Meniel V, Wilkins JA, Cole AM, Oien KA, Marsh V, Jamieson TJ, Guerra C, Ashton GH, Barbacid M, Clarke AR: Loss of Apc allows phenotypic manifestation of the transforming properties of an endogenous K-ras oncogene in vivo. Proc Natl Acad Sci U S A. 2006, 103: 14122-14127. 10.1073/pnas.0604130103.
He TC, Sparks AB, Rago C, Hermeking H, Zawel L, da Costa LT, Morin PJ, Vogelstein B, Kinzler KW: Identification of c-MYC as a target of the APC pathway. Science. 1998, 281: 1509-1512. 10.1126/science.281.5382.1509.
Adhikary S, Eilers M: Transcriptional regulation and transformation by Myc proteins. Nat Rev Mol Cell Biol. 2005, 6: 635-645. 10.1038/nrm1703.
Denko NC, Giaccia AJ, Stringer JR, Stambrook PJ: The human Ha-ras oncogene induces genomic instability in murine fibroblasts within one cell cycle. Proc Natl Acad Sci U S A. 1994, 91: 5124-5128. 10.1073/pnas.91.11.5124.
Soengas MS, Lowe SW: p53 and p73: seeing double?. Nat Genet. 2000, 26: 391-392. 10.1038/82497.
Quelle DE, Zindy F, Ashmun RA, Sherr CJ: Alternative reading frames of the INK4a tumor suppressor gene encode two unrelated proteins capable of inducing cell cycle arrest. Cell. 1995, 83: 993-1000. 10.1016/0092-8674(95)90214-7.
Reisman D, Elkind NB, Roy B, Beamon J, Rotter V: c-Myc trans-activates the p53 promoter through a required downstream CACGTG motif. Cell Growth Differ. 1993, 4: 57-65.
Roy B, Beamon J, Balint E, Reisman D: Transactivation of the human p53 tumor suppressor gene by c-Myc/Max contributes to elevated mutant p53 expression in some tumors. Mol Cell Biol. 1994, 14: 7805-7815.
Vafa O, Wade M, Kern S, Beeche M, Pandita TK, Hampton GM, Wahl GM: c-Myc can induce DNA damage, increase reactive oxygen species, and mitigate p53 function: a mechanism for oncogene-induced genetic instability. Mol Cell. 2002, 9: 1031-1044. 10.1016/S1097-2765(02)00520-8.
Collins K, Jacks T, Pavletich NP: The cell cycle and cancer. Proc Natl Acad Sci U S A. 1997, 94: 2776-2778. 10.1073/pnas.94.7.2776.
Ren B, Cam H, Takahashi Y, Volkert T, Terragni J, Young RA, Dynlacht BD: E2F integrates cell cycle progression with DNA repair, replication, and G(2)/M checkpoints. Genes Dev. 2002, 16: 245-256. 10.1101/gad.949802.
Mundle SD, Saberwal G: Evolving intricacies and implications of E2F1 regulation. Faseb J. 2003, 17: 569-574. 10.1096/fj.02-0431rev.
Lazzerini Denchi E, Helin K: E2F1 is crucial for E2F-dependent apoptosis. EMBO Rep. 2005, 6: 661-668. 10.1038/sj.embor.7400452.
Stiewe T, Putzer BM: Role of the p53-homologue p73 in E2F1-induced apoptosis. Nat Genet. 2000, 26: 464-469. 10.1038/82617.
Fujisaki T, Tanaka Y, Fujii K, Mine S, Saito K, Yamada S, Yamashita U, Irimura T, Eto S: CD44 stimulation induces integrin-mediated adhesion of colon cancer cell lines to endothelial cells by up-regulation of integrins and c-Met and activation of integrins. Cancer Res. 1999, 59: 4427-4434.
Matusan K, Dordevic G, Mozetic V, Lucin K: Expression of osteopontin and CD44 molecule in papillary renal cell tumors. Pathol Oncol Res. 2005, 11: 108-113.
Hediger MA, Romero MF, Peng JB, Rolfs A, Takanaga H, Bruford EA: The ABCs of solute carriers: physiological, pathological and therapeutic implications of human membrane transport proteinsIntroduction. Pflugers Arch. 2004, 447: 465-468. 10.1007/s00424-003-1192-y.
Mizuarai S, Miki S, Araki H, Takahashi K, Kotani H: Identification of dicarboxylate carrier Slc25a10 as malate transporter in de novo fatty acid synthesis. J Biol Chem. 2005, 280: 32434-32441. 10.1074/jbc.M503152200.
Tisdale MJ: Metabolic abnormalities in cachexia and anorexia. Nutrition. 2000, 16: 1013-1014. 10.1016/S0899-9007(00)00409-3.
Vahsen N, Cande C, Briere JJ, Benit P, Joza N, Larochette N, Mastroberardino PG, Pequignot MO, Casares N, Lazar V, Feraud O, Debili N, Wissing S, Engelhardt S, Madeo F, Piacentini M, Penninger JM, Schagger H, Rustin P, Kroemer G: AIF deficiency compromises oxidative phosphorylation. Embo J. 2004, 23: 4679-4689. 10.1038/sj.emboj.7600461.
Kroemer G: Mitochondria in cancer. Oncogene. 2006, 25: 4630-4632. 10.1038/sj.onc.1209589.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/7/109/prepub
This work was supported by funding from the Agency for Science, Technology and Research (A*STAR) of Singapore and the NIH/NHGRI (1R01HG003521-01) to YR. Data was produced through the collaboration between the Genome Institute of Singapore (GIS) and Riken. The authors want to thank Riken Genome Exploration Research Group and Genome Science Group for the courtesy of providing material and the Genome Technology and Biology Group at GIS for library construction and sequencing, especially Melissa Jane Fullwood for critical reading of the manuscript. We also thank Mr. K.R. Govindarajan for processing sequence data.
The author(s) declare that they have no competing interests.
KPC conceptualized the approach of using PET transcriptome data in conjunction with KEGG database for pathway and library comparisons, and analyzed data. PA setup the local KEGG pathway database, and coded programs for pathway analysis. HX conducted statistical analyses. AT coded programs for data analysis and visualization. PN constructed libraries. RY and CLW contributed to the PET method development. ETBL provided some ideas for data analysis. CLW also involved in manuscript preparation. WKKS developed the CSA approach for PET mapping. KPC wrote the paper. All authors have read and approved the final manuscript.
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Chiu, K.P., Ariyaratne, P., Xu, H. et al. Pathway aberrations of murine melanoma cells observed in Paired-End diTag transcriptomes. BMC Cancer 7, 109 (2007). https://doi.org/10.1186/1471-2407-7-109
- Melanoma Cell
- Proliferate Cell Nuclear Antigen
- B16F1 Melanoma
- B16F1 Melanoma Cell