Onconase responsive genes in human mesothelioma cells: implications for an RNA damaging therapeutic agent
BMC Cancer volume 10, Article number: 34 (2010)
Onconase represents a new class of RNA-damaging drugs. Mechanistically, Onconase is thought to internalize, where it degrades intracellular RNAs such as tRNA and double-stranded RNA, and thereby suppresses protein synthesis. However, there may be additional or alternative mechanism(s) of action.
In this study, microarray analysis was used to compare gene expression profiles in untreated human malignant mesothelioma (MM) cell lines and cells exposed to 5 μg/ml Onconase for 24 h. A total of 155 genes were found to be regulated by Onconase that were common to both epithelial and biphasic MM cell lines. Some of these genes are known to significantly affect apoptosis (IL-24, TNFAIP3), transcription (ATF3, DDIT3, MAFF, HDAC9, SNAPC1) or inflammation and the immune response (IL-6, COX-2). RT-PCR analysis of selected up- or down-regulated genes treated with varying doses and times of Onconase generally confirmed the expression array findings in four MM cell lines.
Onconase treatment consistently resulted in up-regulation of IL-24, previously shown to have tumor suppressive activity, as well as ATF3 and IL-6. Induction of ATF3 and the pro-apoptotic factor IL-24 by Onconase was highest in the two most responsive MM cell lines, as defined by DNA fragmentation analysis. In addition to apoptosis, gene ontology analysis indicated that pathways impacted by Onconase include MAPK signaling, cytokine-cytokine-receptor interactions, and Jak-STAT signaling.
These results provide a broad picture of gene activity after treatment with a drug that targets small non-coding RNAs and contribute to our overall understanding of MM cell response to Onconase as a therapeutic strategy. The findings provide insights regarding mechanisms that may contribute to the efficacy of this novel drug in clinical trials of MM patients who have failed first line chemotherapy or radiation treatment.
Onconase (ranpirnase), an extremely stable endoribonuclease that was originally isolated from the oocytes of Rana pipiens, is part of a paradigm shift in drug development. The intracellular target is RNA, not DNA or protein. Onconase damage to tRNA [1–3] causes activation of the caspase cascade in mammalian cells and results in apoptosis [2, 4]. Although Onconase cleaves tRNA at unique sites compared to other pancreatic type RNases , inhibition of protein synthesis due to tRNA damage cannot explain many activities of Onconase [2, 6]. Therefore, another postulated Onconase mechanism is that it acts as an intracellular catalyst for the generation of interfering RNAs (RNAi) which could also trigger apoptosis depending upon the microenvironment of the cell . Further information on the structure and therapeutic potential of Onconase is found in several recent reviews [7–9].
Therapeutic treatment of malignant mesothelioma (MM) remains a major challenge. Prior studies have shown that Onconase induces apoptosis in MM cells and that this effect is tumor cell specific . A cooperative effect was observed between small molecule inhibitors of phosphatidylinositol 3-kinase (PI3K) and Onconase in the killing of MM cells. In MM cells with increased PI3K activity, Rosiglitazone acted cooperatively with Onconase to inhibit cell proliferation . Additional studies are needed to understand the action of Onconase in MM cells. These studies may lead to new combinatorial strategies that may enhance the responsiveness of MM cells to treatment, given that in other tumor types Onconase was shown to be strongly synergistic when combined with other antitumor agents.
For example, the reduction of NF-κB expression in lymphocytic leukemia cells by Onconase appeared to be associated with growth suppression, suggesting that NF-κB and its turnover are important determinants in the anti-proliferative/apoptotic effects of Onconase in this tumor cell context . Also, a positive drug interaction was shown between Onconase and Cepharanthine cytotoxicity when used in combination on various tumor cell lines, and it was postulated that increased cytotoxicity may be associated with Onconase activity in targeting microRNAs and/or NF-κB .
Preclinical work coupled with a novel mechanism led to Phase I and Phase I/II clinical trials of Onconase as a single therapeutic agent in patients with a variety of solid tumors [14–16]. Currently, investigations have progressed to confirmatory Phase IIIb clinical trials for the treatment of unresectable MM, one as a single agent  and another in combination with doxorubicin. The latter study included subjects with pleural and/or peritoneal MM who had failed one prior systemic therapy, and it was conducted at 27 centers in the U.S. and 31 centers outside the U.S. . Although now closed to enrolment, the FDA approval of premetrexed (Alimta) + cisplatin as front-line treatment had an impact on the type of subjects accrued to this trial and thus included a sizeable population of subjects with previous chemotherapy failure (total, N = 130; Onconase + doxorubicin, N = 65; doxorubicin, N = 65). Hence, the statistical plan provided for an analysis of outcomes based on prior chemotherapy failure, and using this pre-specified comparison, subjects showed a clinically meaningful and statistically significant difference in overall survival favouring the combination of Onconase + Doxorubicin (hazard ratio 1.45; p = 0.033). The survival difference was robust and the statistical significant effect was maintained in a stratified Cox model (hazard ratio 1.548; p = 0.027) .
Since Onconase is in advanced clinical development, it is even more important to understand the underlying biological phenomenon connected with its mode of action. Expression profiling is a useful approach to identify pathways altered upon exposure to drugs. Here, a global transcriptional analysis using expression arrays was used to simultaneously search thousands of genes to delineate those that are differentially regulated by Onconase in MM cells. We have identified a subset of genes likely to be generally important in the response of MM cells to Onconase, since they were common to cell lines derived from both epithelial and biphasic tumors. Elucidation of individual genes and their association with signaling pathways should facilitate the development of therapeutic strategies to improve the clinical performance of Onconase.
Cell Lines, Reagents and Treatment
Human MM cell lines M25, M29, M35, M42 and M49 (kindly provided by S.C. Jhanwar ) were from pleural tumors. Established cell lines (>passage 10) were propagated in 10 cm dishes (Falcon) in RPMI medium containing 10% FBS. M25 and M35 exhibited biphasic characteristics, whereas M29, M42 and M49 were epithelial in origin. Lyophilized Onconase, from Alfacell Corporation, was dissolved in sterile distilled, deionized water and prepared in medium (RPMI + 10% FBS).
Cell Viability Assay
An MTS assay (Promega CellTiter 96-AQueous One Solution Assay) was used to analyze the effect of Onconase on cell viability. Cells were cultured overnight in 96-well plates (~1 × 104 cells/well). Cell viability was assessed after the addition of Onconase at the indicated concentrations for 24, 48 or 72 h. The number of viable cells was assessed by determination of the A490 nm of the dissolved formazan product after addition of MTS for 1 h as described by the manufacturer (Promega).
Expression Array Analysis
At ~50 to 80% confluence, all MM cell lines were incubated with Onconase (5 μg/ml) for 24 h in the presence of growth medium containing 10% fetal bovine serum. The concentration and duration of the Onconase treatment for the expression array were selected based on our MTS results (Figure 1), in which there was ≤20% loss of cell viability across most MM cell lines. Cells were harvested, and total RNA was isolated with Trizol, according to the manufacturer's instructions (Invitrogen). Only RNA isolates that had an acceptable concentration and absorbance 260/280 nm ratio from M25, M29 and M49 cells were used.
Expression profiles were generated using Affymetrix Human Genome U133 plus 2.0 Gene Chips (HG U133 plus 2.0) according to the Affymetrix Eukaryote One-Cycle Target Labelling Assay. Briefly, 5 μg of total RNA was used to synthesize double-stranded cDNA, which was in vitro transcribed into biotinylated cRNA. The biotinylated cRNA was fragmented and hybridized to GeneChips for 16 hours at 45°C in an Affymetrix Hybridization Oven 640. Arrays were then washed and stained on an Affymetrix Fluidics Station 450 using Affymetrix fluidics protocol EukGE-WS2v5, and subsequently scanned on an Affymetrix GeneChip Scanner 3000 to obtain fluorescence intensities. Relative expression values were generated for each transcript using the Affymetrix MAS5.0 algorithm in GeneChip® Operating Software (GCOS) Version 1.4 with All Probe Sets Scaling of 500. Data have been deposited in NCBI's Gene Expression Omnibus repository http://www.ncbi.nih.gov/geo/ and are available under the accession number "GSE17009".
Quantitative Real-Time PCR
M49 cells exhibited poor growth characteristics when thawed from multiple frozen isolates and were not used for further analysis. M25, M29, M35 and M42 were used for quantitative real-time PCR. Following treatment with Onconase, both adherent and floating cells were collected and used for RNA isolation. Reverse transcription of RNA to cDNA was performed using a High Capacity cDNA Archive Kit (Applied Biosystems) according to the manufacturer's instructions. Reactions for quantitative real-time PCR were prepared in a 25 μl total volume with TaqMan® Universal PCR MasterMix (Applied Biosystems), TaqMan® Gene Expression Assays (Applied Biosystems) for PTGS2 (COX-2; assay ID: Hs00153133_m1), IL-6 (assay ID: Hs00174131_m1), IL-24 (assay ID: Hs01114274_m1), ATF3 (assay ID: Hs00231069_m1), PTOV1 (assay ID: Hs00363189_g1) or beta-2 microglobulin (assay ID: Hs99999907_m1) and 10-20 ng cDNA per the manufacturer's specifications. Thermal cycling and detection of amplification products were carried out on an ABI PRISM ® 7900 Sequence Detection System (Applied Biosystems).
The average CT (threshold cycle) values for the target genes and for beta-2 microglobulin were calculated from the replicate values generated for each sample. The average CT value for the housekeeping gene, beta-2 microglobulin, was subtracted from the average CT value for each target gene in order to normalize values for the amount of total cDNA added to the reaction. Relative quantitation (i.e., fold-difference in expression levels) between untreated and treated samples was calculated using the Ct method (Applied Biosystems User Bulletin Number 2).
DNA Fragmentation Assay
MM cells were treated with 5 μg/ml Onconase for 24, 48 and 72 h. Adherent and floating cells were collected from untreated or treated cell cultures. Cells were lysed and processed for DNA fragmentation using a Cell Death Detection ELISA Kit (Roche Diagnostics) as per the manufacturer's instructions.
Gene Ontology Analysis
Gene names were entered into the GeneInfoVis program : http://genenet2.utmem.edu/geneinfoviz/search.php. The resulting matching categories were separated according to the Gene Ontology groupings  based on the three broad ontology categories, cellular component [C], molecular function [F] or biological process [P] and then counted. Onto-Express (OE, ) was also used to identify those biological processes that were impacted significantly by the Onconase regulated genes (ORGs). Statistical significance values were calculated for each category using either a hypergeometric or binomial distribution depending on the number of genes on the array, as described elsewhere .
Assignment of Genes to Known Pathways
Two principal databases that assign proteins to pathways, KEGG  and BioCarta http://www.biocarta.com were accessed through the Cancer Genome Anatomy Project http://cgap.nci.nih.gov/Pathways/Pathway_Searcher. The KEGG and BioCarta resources provide a reference knowledge base for linking genomes to biological systems. The network representation of linkages between ORGs and published pathways was constructed and drawn using the program Cytoscape-2.6.0 available online at http://www.cytoscape.org.
Onconase inhibits MM cell viability
Similar to previous studies , cell viability assays showed that some MM cell lines are more responsive to Onconase than others. As expected, response was dose and time dependent, with the greatest effect on cell viability observed after 48 to 72 h (Figure 1). None of the Onconase-treated cells reached an IC50 dose response at the 24 h time point. As an unbiased approach to examine gene expression in MM cells in response to Onconase prior to a significant loss of viability, we choose to analyze the 24 h time point across a panel of cell lines that exhibited variable response to Onconase. Subsequent studies validated that a subset of gene expression changes were up-regulated in response to Onconase in MM cell lines.
Onconase Regulated Genes (ORGs) common to three MM cell lines detected by microarray-based expression analysis
There is precedent for the use of microarrays to identify specific genes that may be important in therapeutic response of MM cells [24, 25]. Here, the underlying molecular mechanisms of Onconase-induced loss of MM cell viability were investigated using expression array technology. To select against individual cell line-specific responses, we analyzed only ORGs common to three different MM cell lines. A comparison of the expression profiles in the Onconase-treated and untreated cells revealed 155 genes that were similarly up- of down-regulated in all three cell lines. Most (66%) of the genes were up-regulated (average increase from untreated cells ranged from 1.2- to 14.6-fold), whereas 34% were down-regulated (average decrease compared to untreated cells ranging from 1.3- to 2.5-fold); this suggests that the primary effect of Onconase is activation of gene expression. Many (52) of the genes were associated with one or more cellular pathways. Potential ORGs common to the three cell lines that increased an average of 3-fold or more after Onconase treatment are shown in Table 1. Some of these genes are known to significantly affect apoptosis (IL-24 and TNFAIP3 p = 0.001), transcription (ATF3, DDIT3, MAFF, HDAC9 and SNAPC1, p = 0.009) and inflammation and the immune response (IL-6, p = 0.01 and COX-2, p = 0.001). Although none of the down-regulated genes averaged a 3-fold decrease, PTOV1 was decreased nearly 2-fold.
Quantitative real-time RT-PCR analysis of gene expression
Messenger RNA expression of four up-regulated genes and one down-regulated gene were examined by quantitative real-time RT-PCR in two of the three MM cell lines used for the microarray analysis (M25 and M29) plus two additional MM cell lines (M35 and M42) (Figure 2). All four cell lines were treated under conditions identical to that used for the microarray analysis. ATF3, IL-24 and IL-6 were among the most highly induced genes detected in the array analysis (Table 1) and were confirmed to be up-regulated by RT-PCR analysis in all MM cell lines tested. COX-2, another up-regulated gene, was validated to be increased in two of four MM cell lines (Figure 2). PTOV1 expression was slightly decreased or unchanged in the four cell lines. Quantitative gene expression changes demonstrated a wide variation among the four individual cell lines but generally were in the same direction as in the array analysis. ATF3 expression increased from 3-fold to more than 400-fold, IL-24 from 2- to nearly 1000-fold, and IL-6 from 2- to nearly 100-fold. In comparison, COX-2 expression increased ~5 -fold in two cell lines and was unchanged or decreased approximately 2-fold in one line (Figure 2).
We also performed an expanded analysis of gene expression in MM cells treated with Onconase at various doses (2.5 to 10 μg/ml), which showed highly reproducible changes (Figure 3). Moreover, RT-PCR performed on MM cell lines treated for varying times (24 to 72 h) with 5 μg/ml Onconase showed remarkably consistent up-regulated expression of IL-24 as well as of ATF3 and IL-6 (Figure 4A). Among the five genes tested, the gene encoding the pro-apoptotic factor IL-24 is noteworthy in that its expression increased with time in three of four cell lines. Interestingly, induction of ATF3 and IL-24 was highest in M35, a highly responsive MM cell line, and lowest in M25, a poorly responsive cell line, as defined by DNA fragmentation analysis (Figure 4B).
Although investigating individual gene expression can provide insights about important aspects of Onconase action, the overall mechanism is a heterogeneous phenomenon that should also be defined by means of biological processes and pathways. The entire group of ORGs common to three MM cell lines was searched to identify genes that could be characterized for a known ontology. The resulting 155 gene name matches (hits) were used to extract the associated ontologies based on three broad ontology categories: the particular part of the cell (cellular component); the activities of individual gene products (molecular function); and their integration with other genes to form a defined function (biological process). Since each ORG could be associated with one or more of these categories, the number of hits is listed and not the number of genes (Additional file 1). The major biological process ontologies (30 or more hits) were related to cell signaling and signal transduction (34 hits), molecular events involving DNA (34 hits), and transcription (60 hits). The individual function of the ORGs favored metal ion binding and transcription and were mainly associated with membranes and the nucleus (Additional file 1). Other significant biological processes (15 or more hits) involved apoptosis, cell cycle, differentiation/development, cell proliferation/growth, processes involving RNA, metabolism/catabolism, transport and protein molecular events such as phosphorylation, assembly, binding and folding. Taken together, these results (Additional file 1) show that ORGs participate in important cellular events, mostly at the level of transcription.
Signaling pathways affected by ORGs in MM cell lines
ORG expression was mapped to known metabolic and regulatory pathways using two principal databases, KEGG and BioCarta. To assign genes from the over- or under-expressed gene probes, 155 usable names were generated after removing duplicates and probes that did not correspond to any known genes. Among the 155 ORGs, there were 52 hits mapped to KEGG and/or BioCarta Pathways. The data clearly show clusters of genes in various pathways. Cell cycle and MAPK-associated genes are two examples. Some of the genes (DUSP6, FAS, HDAC9, IL-6, JAK1, JUN, PLCB4) are linked to 10 or more known pathways while others such as (CRY1, DIC1, GTF2H1, JAG1, MAFF, NPPB, PBEF1, PCLO, QPRT, RB1CC1, SAT, SIC2A3, SULT1A3, SUOX, TALDO1) are only mapped to one. Overall, the data show that after 24 h of treatment, Onconase affects many of the genes involved in classical pathways that control cell growth and death. Some genes, for example CRY1, mapped to unusual pathways such as circadian rhythm. While the importance of this pathway to Onconase mechanism of action is unknown, further research may link CRY1 to other more obviously relevant pathways.
Genes involved in MAPK signaling (p = 0.00006) and cytokine-cytokine-receptor interaction (p = 0.006) were very significantly impacted by Onconase. The ORGs involved are listed in Table 2 and depicted in Figure 5. Jak-STAT (p = 0.06) signaling ORGs are also shown in Table 2 and Figure 5. The p values of the other possible pathway gene clusters ranged from p = 0.2 (Wnt signaling) to p = 0.4 (cell cycle) to p = 0.9 (regulation of actin cytoskeleton).
Interaction of ORGs in MM cell lines
In addition to Figure 5, Table 3 further illustrates the interconnected relationship of ORGs and known pathways. More than half of the 35 shared pathways involve signaling. One cluster (data not shown) contained CYP1A1 and COX-2, two of the more highly up-regulated ORGs (Table 1). CYP1A1 (tryptophan, linoleic and fatty acid metabolism pathways) is connected via the arachidonic acid metabolism pathway to COX-2 (eicosanoid metabolism pathway). The ORGs in the cytokine-cytokine receptor and Jak-STAT pathways are directly linked through shared genes, e.g. IL-6, IL-6st and IL-24. Other relevant linkages are through second or third order shared genes and pathways. For example, MAPK to DUSP6 is linked further to the cytokine-cytokine receptor pathways via TGFβ signaling (Figure 5) and INHBA. Numerous other linkages can also be seen. Thus, Onconase-induced signals are propagated through the cellular membrane and intracellular milieu. This implies that Onconase initiates a cascade of ORG-mediated responses leading to growth inhibition and apoptosis in human MM cell lines.
Microarray technology is a powerful tool for investigating cellular responses to drugs because it monitors thousands of genes simultaneously. The present study is the first to use microarray-derived transcriptional profiling to identify ORGs common to multiple human MM cell lines. Many ORGs are associated with cellular signal transduction, proliferation and differentiation. Transcription and DNA processes connected mainly with membranes and the nucleus were the most affected ontologies. All of this is consistent with the reprogramming of cellular regulatory systems by Onconase. Important new insights into Onconase mechanism include the convergence of cellular responses to RNA damaging and standard DNA-damaging drugs, and ORG interaction with genes involved in MAPK signaling.
IL-24 was originally identified as mda-7, a gene selectively up-regulated during terminal differentiation of melanoma cells  and later classified as a member of the IL-10 family . Recently, an adenovirus encoding the IL-24 gene has been shown to have selective anticancer effects in cell culture and in animal models (reviewed in ). IL-24 also sensitizes cells to radiation and other conventional therapies, inhibits angiogenesis and exhibits bystander effects in animal models. A replication-incompetent adenovirus encoding IL-24 (Ad. mda-7) has undergone evaluation in a Phase I clinical trial and showed rapid clinical advancement . However, gene therapy protocols exhibit limitations associated with local delivery and adverse immune reactions. The specific high level induction of IL-24 by NSAIDs has generated enthusiasm for increasing systemic levels of IL-24 that might be effective without the limitations of adenoviral delivery . The present work shows that Onconase also induces IL-24 mRNA in MM cells. This finding has implications for understanding the basis for the selective antitumor effects of Onconase in cell culture experiments  and its well tolerated activity in patients . Up-regulation of IL-24 might also be related to the enhanced radiation sensitivity of non-small cell lung cancer (NSCLC) cells treated with Onconase , because IL-24 has been shown to sensitize NSCLC xenograft tumors to radiation .
In view of these findings, combination therapy with Onconase and NSAIDs should be considered in treating MM patients if preclinical efficacy and safety studies warrant it. NSAIDs decrease the expression of COX-2 and genes involved in the formation of inflammatory prostaglandins from polyunsaturated fatty acids such as arachidonic acid  in MM cells . Thus, the use of NSAIDS could moderate any potential effects of Onconase on COX-2 expression, while the combined effect of both agents might induce more IL-24 than either agent alone. Indeed, an NSAID has been shown to increase ectopic expression of IL-24 that augmented adenovirus delivery leading to the proposed use of more than one inducer of IL-24 to achieve superphysiological levels of this pro-apoptotic factor in tumors .
ATF3 has not previously been associated with Onconase activity. ATF3 (activating transcription factor 3), a member of the ATF/CREB family of transcription factors, participates in cellular processes to adapt to extra/intracellular changes . It is expressed at low levels in normal and quiescent cells but can be induced by a variety of extracellular agents, including radiation  and other genotoxic stress signals . The consequences of ATF3 induction result in tumor growth inhibition and suppression of Ras-stimulated tumorigenesis [37, 38]. ATF3 mRNA was up-regulated in MM cell lines used in the microarray expression analysis as well as in two additional human MM cell lines examined, indicating that the Onconase up-regulation of ATF3 is not cell line specific.
Chemotherapeutic agents that damage DNA also induce ATF3. Camptothecin and etoposide, DNA topoisomerase inhibitors , as well as the anthracycline antibiotic doxorubicin  have all been shown to induce ATF3 in tumor cells. Stably or transiently transfected ATF3 accelerated drug-induced apoptosis . 5-Fluorouracil (5-FU) is used in the treatment of gastrointestinal, breast, and head and neck cancers . Treatment of colon cancer cell lines with 5-FU induced ATF3 along with other DNA damage response genes (GADD34, GADD45α, PCNA) .
Overexpression of more than one GADD gene causes synergistic growth inhibition and/or apoptosis . Therefore the combined induction of GADD45α, GADD45β and GADD153 by Onconase seen in our microarray analysis suggests these genes may act synergistically to inhibit MM cell viability.
ORGs very significantly affect MAPK signaling in MM cells. This is consistent with MAPK regulation of ATF3  as well as the GADD genes [44, 45]. Sequential activation of protein kinases within the MAPK pathways is a common mechanism of signal transduction in many cellular processes including the stress response, and apoptosis . In fact, MAPK signaling is common to the action of many divergent chemotherapeutic agents (reviewed in ). In addition to MAPK, AKT signaling has been shown to influence tumor cell responsiveness to chemotherapeutics. Although not addressed in this study, a previous report noted that Onconase induces apoptosis in MM cells, and that MM cells with the highest AKT activation were more resistant to the drug .
Recently, genotoxic stress and apoptosis were also associated with RNA genes . MicroRNAs (miRNAs), products of non-coding RNA genes, that are transcribed by RNA polymerase II, are processed and exported to the cytoplasm where they bind to the 3' UTRs of target mRNAs to inhibit translation . Numerous miRNAs are deregulated in human cancers, consequently affecting their target mRNAs and subsequent protein products . Onconase is known to damage non-coding RNA (i.e., tRNA) to inhibit protein synthesis, but its effect on apoptosis has been attributed, at least partly, to other unknown cellular targets , possibly miRNAs . Interestingly, nine ORGs affect transcription from the RNA polymerase II promoter, and one of these, CEBPB, is a target of miRNA-155 . Moreover, miRNA-155 is up-regulated in some cancers , and its levels are decreased by Onconase in MM cells (K. Shogen, unpublished data).
Collectively, the results presented here show that a RNA-damaging drug can impact many of the same important genes and pathways as standard chemotherapeutics. Future studies are needed to address whether ATF3 and IL-24 act as key pro-apoptotic genes to mediate the chemotherapeutic response of MM cells to Onconase. Moreover, it remains to be determined whether up-regulation of IL-6 and COX-2 expression could impact the responsiveness of MM patients to Onconase. Targeting these pro-inflammatory proteins may lead to improvements in Onconase treatment protocols. Current findings implicate several new genes in the response of MM cells to Onconase, and further studies are expected to elucidate whether up-regulation of these genes may serve as new biomarkers of response to Onconase.
- CT :
nonsteroidal anti-inflammatory drugs
Onconase regulated genes
Lin JJ, Newton DL, Mikulski SM, Kung HF, Youle RJ, Rybak SM: Characterization of the mechanism of cellular and cell free protein synthesis inhibition by an anti-tumor ribonuclease. Biochem Biophys Res Commun. 1994, 204 (1): 156-162. 10.1006/bbrc.1994.2439.
Iordanov MS, Ryabinina OP, Wong J, Dinh TH, Newton DL, Rybak SM, Magun BE: Molecular determinants of apoptosis induced by the cytotoxic ribonuclease onconase: evidence for cytotoxic mechanisms different from inhibition of protein synthesis. Cancer Res. 2000, 60 (7): 1983-1994.
Saxena SK, Sirdeshmukh R, Ardelt W, Mikulski SM, Shogen K, Youle RJ: Entry into cells and selective degradation of tRNAs by a cytotoxic member of the RNase A family. J Biol Chem. 2002, 277 (17): 15142-15146. 10.1074/jbc.M108115200.
Grabarek J, Ardelt B, Du L, Darzynkiewicz Z: Activation of caspases and serine proteases during apoptosis induced by onconase (Ranpirnase). Exp Cell Res. 2002, 278 (1): 61-71. 10.1006/excr.2002.5568.
Suhasini AN, Sirdeshmukh R: Transfer RNA cleavages by onconase reveal unusual cleavage sites. J Biol Chem. 2006, 281 (18): 12201-12209. 10.1074/jbc.M504488200.
Ardelt B, Ardelt W, Darzynkiewicz Z: Cytotoxic ribonucleases and RNA interference (RNAi). Cell Cycle. 2003, 2 (1): 22-24.
Saxena SK, Shogen K, Ardelt W: Onconase and its therapeutic potential. Lab Med. 2003, 34: 380-387. 10.1309/3TD26GXN65GEC1BG.
Costanzi J, Sidransky D, Navon A, Goldsweig H: Ribonucleases as a novel pro-apoptotic anticancer strategy: review of the preclinical and clinical data for ranpirnase. Cancer Invest. 2005, 23 (7): 643-650. 10.1080/07357900500283143.
Lee JE, Raines RT: Ribonucleases as novel chemotherapeutics: the ranpirnase example. BioDrugs. 2008, 22 (1): 53-58. 10.2165/00063030-200822010-00006.
Ramos-Nino ME, Vianale G, Sabo-Attwood T, Mutti L, Porta C, Heintz N, Mossman BT: Human mesothelioma cells exhibit tumor cell-specific differences in phosphatidylinositol 3-kinase/AKT activity that predict the efficacy of Onconase. Mol Cancer Ther. 2005, 4 (5): 835-842. 10.1158/1535-7163.MCT-04-0243.
Ramos-Nino ME, Littenberg B: A novel combination: ranpirnase and rosiglitazone induce a synergistic apoptotic effect by down-regulating Fra-1 and Survivin in cancer cells. Mol Cancer Ther. 2008, 7 (7): 1871-1879. 10.1158/1535-7163.MCT-08-0308.
Tsai SY, Ardelt B, Hsieh TC, Darzynkiewicz Z, Shogen K, Wu JM: Treatment of Jurkat acute T-lymphocytic leukemia cells by onconase (Ranpirnase) is accompanied by an altered nucleocytoplasmic distribution and reduced expression of transcription factor NF-kappaB. Int J Oncol. 2004, 25 (6): 1745-1752.
Ita M, Halicka HD, Tanaka T, Kurose A, Ardelt B, Shogen K, Darzynkiewicz Z: Remarkable enhancement of cytotoxicity of onconase and cepharanthine when used in combination on various tumor cell lines. Cancer Biol Ther. 2008, 7 (7): 1104-1108.
Mikulski SM, Grossman AM, Carter PW, Shogen K, Costanzi JJ: Phase 1 human clinical trial of ONCONASE (P-30 protein) administered intravenously on a weekly schedule in cancer patients with solid tumors. Int J Cancer. 1993, 3: 57-64. 10.1046/j.1525-1438.1993.03010057.x.
Vogelzang NJ, Aklilu M, Stadler WM, Dumas MC, Mikulski SM: A phase II trial of weekly intravenous ranpirnase (Onconase), a novel ribonuclease in patients with metastatic kidney cancer. Invest New Drugs. 2001, 19 (3): 255-260. 10.1023/A:1010633004157.
Mikulski SM, Costanzi JJ, Vogelzang NJ, McCachren S, Taub RN, Chun H, Mittelman A, Panella T, Puccio C, Fine R, et al: Phase II trial of a single weekly intravenous dose of ranpirnase in patients with unresectable malignant mesothelioma. J Clin Oncol. 2002, 20 (1): 274-281. 10.1200/JCO.20.1.274.
Vogelzang N, Taub R, Shin D, Costanzi J, Pass H, Gutheil J, Georgiadis M, McAndrew P, Kelly K, Chun H, et al: Phase III randomized trial of Ranpirnase (Onc) vs doxorubicin (DOX) in patients with unresectable malignant mesothelioma: analysis of survival [abstract]. Proc Am Spc Clin Oncol. 2000, 19: 577a-
Reck M, Krzakowski M, Jassem J, Eschbach C, Kozielski J, Costanzi JJ, Gatzemeier U, Shogen K, von Pawel J: Randomized, multicenter phase III study of ranpirnase plus doxorubicin (DOX) versus DOX in patients with unresectable malignant mesothelioma (MM) [abstract]. J Clin Oncol. 2009, 27: 15s-10.1200/JCO.2007.14.5466.
Cheng JQ, Jhanwar SC, Klein WM, Bell DW, Lee W-C, Altomare DA, Nobori T, Olopade OI, Buckler AJ, Testa JR: p16 alterations and deletion mapping of 9p21-p22 in malignant mesothelioma. Cancer Res. 1994, 15: 5547-5551.
Zhou M, Cui Y: GeneInfoViz: constructing and visualizing gene relation networks. In Silico Biol. 2004, 4 (3): 323-333.
Ashburner M, Ball CA, Blake JA, Botstein D, Butler H, Cherry JM, Davis AP, Dolinski K, Dwight SS, Eppig JT, et al: Gene ontology: tool for the unification of biology. The Gene Ontology Consortium. Nat Genet. 2000, 25 (1): 25-29. 10.1038/75556.
Draghici S, Khatri P, Bhavsar P, Shah A, Krawetz SA, Tainsky MA: Onto-Tools, the toolkit of the modern biologist: Onto-Express, Onto-Compare, Onto-Design and Onto-Translate. Nucleic Acids Res. 2003, 31 (13): 3775-3781. 10.1093/nar/gkg624.
Kanehisa M, Goto S, Hattori M, Aoki-Kinoshita KF, Itoh M, Kawashima S, Katayama T, Araki M, Hirakawa M: From genomics to chemical genomics: new developments in KEGG. Nucleic Acids Res. 2006, D354-357. 10.1093/nar/gkj102. 34 Database
Ramos-Nino ME, Scapoli L, Martinelli M, Land S, Mossman BT: Microarray analysis and RNA silencing link fra-1 to cd44 and c-met expression in mesothelioma. Cancer Res. 2003, 63 (13): 3539-3545.
Gordon GJ, Jensen RV, Hsiao LL, Gullans SR, Blumenstock JE, Richards WG, Jaklitsch MT, Sugarbaker DJ, Bueno R: Using gene expression ratios to predict outcome among patients with mesothelioma. J Natl Cancer Inst. 2003, 95 (8): 598-605.
Jiang H, Lin J, Su ZZ, Herlyn M, Kerbel RS, Weissman BE, Welch DR, Fisher PB: The melanoma differentiation-associated gene mda-6, which encodes the cyclin-dependent kinase inhibitor p21, is differentially expressed during growth, differentiation and progression in human melanoma cells. Oncogene. 1995, 10 (9): 1855-1864.
Wang M, Liang P: Interleukin-24 and its receptors. Immunology. 2005, 114 (2): 166-170. 10.1111/j.1365-2567.2005.02094.x.
Sarkar D, Lebedeva IV, Gupta P, Emdad L, Sauane M, Dent P, Curiel DT, Fisher PB: Melanoma differentiation associated gene-7 (mda-7)/IL-24: a 'magic bullet' for cancer therapy?. Expert Opin Biol Ther. 2007, 7 (5): 577-586. 10.1517/147125188.8.131.527.
Zerbini LF, Czibere A, Wang Y, Correa RG, Otu H, Joseph M, Takayasu Y, Silver M, Gu X, Ruchusatsawat K, et al: A novel pathway involving melanoma differentiation associated gene-7/interleukin-24 mediates nonsteroidal anti-inflammatory drug-induced apoptosis and growth arrest of cancer cells. Cancer Res. 2006, 66 (24): 11922-11931. 10.1158/0008-5472.CAN-06-2068.
Smith MR, Newton DL, Mikulski SM, Rybak SM: Cell cycle-related differences in susceptibility of NIH/3T3 cells to ribonucleases. Exp Cell Res. 1999, 247 (1): 220-232. 10.1006/excr.1998.4317.
Lee I, Kim DH, Sunar U, Magnitsky S, Shogen K: The therapeutic mechanisms of ranpirnase-induced enhancement of radiation response on A549 human lung cancer. In Vivo. 2007, 21 (5): 721-728.
Nishikawa T, Ramesh R, Munshi A, Chada S, Meyn RE: Adenovirus-mediated mda-7 (IL24) gene therapy suppresses angiogenesis and sensitizes NSCLC xenograft tumors to radiation. Mol Ther. 2004, 9 (6): 818-828. 10.1016/j.ymthe.2004.03.014.
Reddy RN, Mutyala R, Aparoy P, Reddanna P, Reddy MR: Computer aided drug design approaches to develop cyclooxygenase based novel anti-inflammatory and anti-cancer drugs. Curr Pharm Des. 2007, 13 (34): 3505-3517. 10.2174/138161207782794275.
Baer AN, Green FA: Cyclooxygenase activity of cultured human mesothelial cells. Prostaglandins. 1993, 46 (1): 37-49. 10.1016/0090-6980(93)90061-B.
Oida Y, Gopalan B, Miyahara R, Inoue S, Branch CD, Mhashilkar AM, Lin E, Bekele BN, Roth JA, Chada S, et al: Sulindac enhances adenoviral vector expressing mda-7/IL-24-mediated apoptosis in human lung cancer. Mol Cancer Ther. 2005, 4 (2): 291-304.
Lu D, Chen J, Hai T: The regulation of ATF3 gene expression by mitogen-activated protein kinases. Biochem J. 2007, 401 (2): 559-567. 10.1042/BJ20061081.
Fan F, Jin S, Amundson SA, Tong T, Fan W, Zhao H, Zhu X, Mazzacurati L, Li X, Petrik KL, et al: ATF3 induction following DNA damage is regulated by distinct signaling pathways and over-expression of ATF3 protein suppresses cells growth. Oncogene. 2002, 21 (49): 7488-7496. 10.1038/sj.onc.1205896.
Lu D, Wolfgang CD, Hai T: Activating transcription factor 3, a stress-inducible gene, suppresses Ras-stimulated tumorigenesis. J Biol Chem. 2006, 281 (15): 10473-10481. 10.1074/jbc.M509278200.
Mashima T, Udagawa S, Tsuruo T: Involvement of transcriptional repressor ATF3 in acceleration of caspase protease activation during DNA damaging agent-induced apoptosis. J Cell Physiol. 2001, 188 (3): 352-358. 10.1002/jcp.1130.
Mallory JC, Crudden G, Oliva A, Saunders C, Stromberg A, Craven RJ: A novel group of genes regulates susceptibility to antineoplastic drugs in highly tumorigenic breast cancer cells. Mol Pharmacol. 2005, 68 (6): 1747-1756.
Longley DB, Harkin DP, Johnston PG: 5-fluorouracil: mechanisms of action and clinical strategies. Nat Rev Cancer. 2003, 3 (5): 330-338. 10.1038/nrc1074.
De Angelis PM, Svendsrud DH, Kravik KL, Stokke T: Cellular response to 5-fluorouracil (5-FU) in 5-FU-resistant colon cancer cell lines during treatment and recovery. Mol Cancer. 2006, 5: 20-10.1186/1476-4598-5-20.
Zhan Q, Lord KA, Alamo I, Hollander MC, Carrier F, Ron D, Kohn KW, Hoffman B, Liebermann DA, Fornace AJ: The gadd and MyD genes define a novel set of mammalian genes encoding acidic proteins that synergistically suppress cell growth. Mol Cell Biol. 1994, 14 (4): 2361-2371.
Oh-Hashi K, Maruyama W, Isobe K: Peroxynitrite induces GADD34, 45, and 153 VIA p38 MAPK in human neuroblastoma SH-SY5Y cells. Free Radic Biol Med. 2001, 30 (2): 213-221. 10.1016/S0891-5849(00)00461-5.
Huether A, Hopfner M, Sutter AP, Baradari V, Schuppan D, Scherubl H: Signaling pathways involved in the inhibition of epidermal growth factor receptor by erlotinib in hepatocellular cancer. World J Gastroenterol. 2006, 12 (32): 5160-5167.
Rubinfeld H, Seger R: The ERK cascade: a prototype of MAPK signaling. Mol Biotechnol. 2005, 31 (2): 151-174. 10.1385/MB:31:2:151.
Olson JM, Hallahan AR: p38 MAP kinase: a convergence point in cancer therapy. Trends Mol Med. 2004, 10 (3): 125-129. 10.1016/j.molmed.2004.01.007.
Chang TC, Wentzel EA, Kent OA, Ramachandran K, Mullendore M, Lee KH, Feldmann G, Yamakuchi M, Ferlito M, Lowenstein CJ, et al: Transactivation of miR-34a by p53 broadly influences gene expression and promotes apoptosis. Mol Cell. 2007, 26 (5): 745-752. 10.1016/j.molcel.2007.05.010.
Negrini M, Ferracin M, Sabbioni S, Croce CM: MicroRNAs in human cancer: from research to therapy. J Cell Sci. 2007, 120 (Pt 11): 1833-1840. 10.1242/jcs.03450.
Ying SY, Chang DC, Lin SL: The microRNA (miRNA): overview of the RNA genes that modulate gene function. Mol Biotechnol. 2008, 38 (3): 257-268. 10.1007/s12033-007-9013-8.
Calin GA, Croce CM: MicroRNA signatures in human cancers. Nat Rev Cancer. 2006, 6 (11): 857-866. 10.1038/nrc1997.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/10/34/prepub
This study was performed with the help of the Genomics Facility at Fox Chase Cancer Center and as such was supported in part by NIH Grants CA06927 and an appropriation from the Commonwealth of Pennsylvania. In addition, JRT and DAA were supported by NIH Grant CA114047 and by a gift from Local No. 14 Mesothelioma Fund of the International Association of Heat and Frost Insulators & Allied Workers in memory of Hank Vaughan and Alice Haas.
The authors declare that they have no competing interests.
DAA, SMR, JRT and KS designed experiments. DAA, JP and MC performed experiments. DAA, SMR, JP, JVM and MC analyzed the data. DAA, SMR, JP and JVM were responsible for data management and preparation of tables and figures. DAA, SMR, JRT and KS wrote the manuscript. All authors read and approved the final manuscript.
Deborah A Altomare, Susanna M Rybak contributed equally to this work.
Electronic supplementary material
About this article
Cite this article
Altomare, D.A., Rybak, S.M., Pei, J. et al. Onconase responsive genes in human mesothelioma cells: implications for an RNA damaging therapeutic agent. BMC Cancer 10, 34 (2010). https://doi.org/10.1186/1471-2407-10-34