- Research article
- Open Access
- Open Peer Review
Up-regulation of CLDN1 in gastric cancer is correlated with reduced survival
© Eftang et al.; licensee BioMed Central Ltd. 2013
- Received: 26 May 2013
- Accepted: 21 November 2013
- Published: 10 December 2013
The genetic changes in gastric adenocarcinoma are extremely complex and reliable tumor markers have not yet been identified. There are also remarkable geographical differences in the distribution of this disease. Our aim was to identify the most differentially regulated genes in 20 gastric adenocarcinomas from a Norwegian selection, compared to matched normal mucosa, and we have related our findings to prognosis, survival and chronic Helicobacter pylori infection.
Biopsies from gastric adenocarcinomas and adjacent normal gastric mucosa were obtained from 20 patients immediately following surgical resection of the tumor. Whole genome, cDNA microarray analysis was performed on the RNA isolated from the sample pairs to compare the gene expression profiles between the tumor against matched mucosa. The samples were microscopically examined to classify gastritis. The presence of H. pylori was examined using microscopy and immunohistochemistry.
130 genes showed differential regulation above a predefined cut-off level. Interleukin-8 (IL-8) and Claudin-1 (CLDN1) were the most consistently up-regulated genes in the tumors. Very high CLDN1 expression in the tumor was identified as an independent and significant predictor gene of reduced post-operative survival. There were distinctly different expression profiles between the tumor group and the control mucosa group, and the histological subsets of mixed type, diffuse type and intestinal type cancer demonstrated further sub-clustering. Up-regulated genes were mapped to cell-adhesion, collagen-related processes and angiogenesis, whereas normal intestinal functions such as digestion and excretion were associated with down-regulated genes. We relate the current findings to our previous study on the gene response of gastric epithelial cells to H. pylori infection.
CLDN1 was highly up-regulated in gastric cancer, and CLDN1 expression was independently associated with a poor post-operative prognosis, and may have important prognostic value. IL-8 and CLDN1 may represent central links between the gene response seen in acute H. pylori infection of gastric epithelial cells, and ultimately gastric cancer.
- Gastric cancer
- Interlukin 8
- Helicobacter pylori
- cDNA microarray
Gastric cancer (GC) is only second to lung cancer in world-wide cancer-related deaths, however there are great geographical differences in GC distribution. Data from 2010 demonstrate that the GC incidence in Norway is very low (males 6.9, females 3.0 per 100.000)  compared to less developed areas, particularly in Eastern Asia, where the incidence is approximately 6-fold (males 42.4, females 18.3 per 100.000) .
Gastric adenocarcinoma is remarkably heterogeneous genetically, cytologically and architecturally compared to other gastrointestinal carcinomas. The search for reliable tumor markers and consistent prognostic indicators has proven difficult. Several authors have attempted to predict GC disease and prognosis based on single or multiple genes [3–8], but there are discrepancies between the studies, and currently no gene signature or biomarkers are in routine clinical use. Understanding the mechanisms underlying gastric cancer is one of the major challenges in cancer genomics. The Lauren classification divides adenocarcinomas into three different histological subtypes: intestinal and diffuse types and a mixed variant , which are thought to take different pathways of carcinogenesis. The intestinal type is attributable to a multistep progression from chronic gastritis through gastric atrophy, metaplasia, dysplasia and ultimately malignant disease . Diffuse types may arise from chronic inflammation without a clear manifestation of intermediate premalignant steps [11–13]. The mixed type shows non-homogenous mixtures of both intestinal and diffuse type architecture, and might represent a separate cancer category with exclusive gene mutations and a more aggressive course [14, 15]. In spite of extensive research into the genetic changes of GC, the mechanisms underlying the disease are still far from understood, and the disease cannot easily be explained by an adenoma-carcinoma model like in colorectal cancer. There are three molecular mechanisms that drive gastric carcinogenesis: Chromosome instability, microsatellite instability and epigenetic alterations . The net result is activation of oncogenes, inactivation of tumor suppressor genes and deregulation of signaling pathways [11, 12]. Aberrant cell cycle regulation and changes in the expression of growth factors and cytokines regulate differentiation and survival of tumor cells. Mutations of cell-adhesion and angiogenic genes play important roles in the invasive and metastatic behavior of GC cells.
The aim of the current study was to identify the most differentially regulated genes in surgically resected gastric adenocarcinoma compared to matched normal mucosa, using whole genome cDNA microarray profiling. We also attempt to identify genes which influence GC prognosis and survival. The results are compared to the gastric epithelial cell gene response to H. pylori infection, which was analyzed in a previously published paper . This study adds support to the significance of IL-8 and CLDN1 in gastric carcinogenesis, as well as demonstrates important genetic changes in GC and their possible relevance to H. pylori infection.
Tissue and patient characteristics
Patient characteristics and clinicopathological features of the 20 gastric tumors used in the study
Females n = 5, males n = 15
Caucasian n = 18, Asian n = 2
Age at surgery
Total: 68.7 years (±12.5)
Females: 65.7 years (±21.8)
Males: 69.7 years (±8.6)
Postoperative survival (deceased individuals)
Total: 13.2 months (±8.8)
Females (n = 4): 16.6 months (±6.4)
Males (n = 10): 12.0 months (±9.7)
Postoperative survival (alive individuals at study end)
Total: 45.8 months (±7.9)
Females (n = 1): 48.0 months
Males (n = 5): 44.9 months (±8.8)
49 mm (±27)
Following resection of the tumor, the principal specimen was subjected to histolopathological examination by two senior specialist pathologists to confirm the diagnosis and classify the tumor according to the Lauren classification . Antral and corpal gastric mucosa were examined for gastritis, atrophy and metaplasia, and the presence or absence of H. pylori was microscopically examined and subsequently identified by immunohistochemistry. The Updated Sydney System was used to classify and grade the degree of gastritis [18, 19].
The study was approved by the Norwegian Regional Committee for Medical and Health Research Ethics (REC South East). All samples and patient data was coded and blinded before analysis.
RNA isolation, quality control and cDNA synthesis
Total RNA was isolated using the RNeasy Blood and tissue kit (Qiagen GmBH, Germany) according to the manufacturer’s standard preparation protocol. RNA concentration and quality were determined using a NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, USA) and Agilent 2100 Bioanalyzer (Agilent Technologies, USA). The RNA integrity number was adequate for cDNA synthesis.
The Illumina TotalPrep RNA amplification Kit (Ambion Inc., USA) was used to amplify RNA for hybridization on Illumina BeadChips. To synthesize first strand cDNA by reverse transcription, we used total RNA from each sample collected above. Following the second strand cDNA synthesis and cDNA purification steps, the in vitro transcription to synthesize cRNA was prepared overnight for 12 hours.
cDNA oligonucleotide microarray analysis
The gene expression profiles were measured using Illumina Human HT-12 v3 Expression BeadChip (Illumina, USA), which enables genome-wide expression analysis (48800 transcripts, corresponding to approximately 37800 genes) of 12 samples in parallel on a single microarray. 35967 of the probes were designed using the RefSeq (build 36.2, release 22) library and 12.837 probes were derived from the UniGene (build 199) database [20, 21].
The presence of H. pylori in the surgical specimens was analyzed using a polyclonal anti-Helicobacter-antibody (Dako, Denmark, code B0471, dilution 1:200). 4 μm sections of formalin-fixed, paraffin-embedded tissue from non-tumorous mucosa were applied on coated slides. Deparaffinization, rehydration and epitope retrieval were performed in a Dako PT Link (Dako, Denmark) at 97°C for 20 min. The immunostaining procedure was carried out in a Dako Autostainer Plus applying the Envision™Flex, High pH system (Dako, Denmark).
Bioinformatics and statistics
R/BioConductor [22, 23] with the package Beadarray  were used for preprocessing of the microarray text data from BeadStudio. Spatial artifacts were removed using BASH  before the expression data were log2-transformed and quantile normalized. The log2 fold change (FC) of each probe on the array within each tissue pair (tumor vs matched normal mucosa) was then calculated, and the data were loaded into the J-express software package . Rank product testing  was then performed to test whether the differential expression between tumor tissue and matched normal mucosa was significant. The differential expression was declared significant if the adjusted p-value, i.e. the FDR q-value, was less than 0.05. Hierarchical clustering was performed using average linkage and Euclidean distance measure. The analyses were performed using the J-express software package .
To produce a reasonably sized list of the most differentially expressed genes, lesser expressed genes were filtered out at a cutoff level of FC > 1.5, producing a list of the 130 most differentially expressed genes. This dataset was imported into Onto-Express and Pathway Express [28, 29], part of the Onto-Tools software suite, for functional analysis, and grouped into Gene Ontology (GO) terms and KEGG (Kyoto Encyclopedia of Genes and Genomes) cellular signaling pathways . Pathway Express calculates an Impact Factor (IF) which is used to rank the affected signaling pathways, based on the fold change, the number of the involved genes in the pathway, and the amount of perturbation of downstream genes .
The dataset was entered into PASW Statistics (SPSS version 18.0.2) to perform bivariate correlation analysis to select genes that associated with clinicopathological parameters. Both Pearson and Spearman correlation coefficients were employed to identify correlating genes. Among genes that correlated, we were particularly interested in those that showed a similar expression in our previously published study of H. pylori-exposed gastric epithelial cells . The selected genes were then subjected to a Cox multivariate regression analysis to investigate whether any of the genes were independent predictors of post-operative survival in the GC patients, independent of histological type, tumor stage and size, nodal disease, and age at surgery. In the one predictor gene that was identified, different cut-off levels were applied to construct high and low expression level groups, before statistical significance between the groups was assessed using a log-rank (Mantel-Cox) test. A Kaplan-Meier survival plot was created to demonstrate the difference in survival between the high- and low-expression groups.
The microarray data are available under the accession number E-MTAB-1440 in the ArrayExpress database .
The most differentially regulated genes in gastric tumor vs control mucosa
Up-regulated genes (n=30)
Down-regulated genes (n=100)
Genes from the current dataset were cross-matched against the most differentially regulated genes identified in our previous study, where gastric epithelial cells were exposed to H. pylori for 24 hours in vitro. Both H. pylori-exposed gastric epithelial cells and the tumor biopsies demonstrated significant up-regulation of five common genes (IL-8, CLDN1, KRT17, CLDN7 and MMP7) and down-regulation of four common genes (GPER, KIAA1324, ADA and SLC9A2).
Gene ontology associations in up-regulated genes
No of genes involved
% of genes involved
Calcium-independent cell-cell adhesion
Collagen catabolic process
Collagen fibril organization
Blood vessel development
Regulation of retroviral genome replication
Responsen to corticosteroid stimulus
Gene ontology associations in down-regulated genes
No of genes involved
% of genes involved
Creatine metabolic process
Cellular aldehyde metabolic process
Regulation of pH
Cobalt ion transport
Morphogenesis of an epithelium
KEGG cellular signaling pathways
KEGG cellular signaling pathways
Cell adhesion molecules (CAMs)
Leukocyte transendothelial migration
Epithelial cell signaling in Helicobacter
TGF-beta signaling pathway
Calcium signaling pathway
Among the total set of the 130 most differentially regulated genes, the FC expression levels of 20 genes showed significant correlation with post-operative survival, 8 genes correlated with histological type, 5 genes correlated with tumor size, and 1 gene correlated with lymph node stage (Additional file 1). Some genes showed correlation with more than one parameter. Because of the moderate sample size (n = 20), a significance level of p < 0.01 was chosen.
Factors influencing survival following surgery for gastric cancer
Correlation coefficient R
CLDN1 expression (log2 fold change)
Lymph node fraction
Age at surgery
Histological type (intestinal type)
Histopathological features of adjacent non-cancerous mucosa
In this study we identified CLDN1 as one of the most consistently up-regulated genes in GC and a strong correlation between up-regulation of CLDN1 and reduced survival in 20 patients with gastric adenocarcinomas. This correlation is even stronger when adjusted for other parameters such as lymph node stage, tumor size and histological type. Our clinical sample size is small, but the results are consistent.
Claudins are proteins involved in cellular tight junctions and are important for the maintenance of normal epithelium, in particular barrier formation, cell polarity and signal transduction. Dysregulation of these genes have been identified in many different cancers. Based on tumor biology, down-regulation of CLDN1 would result in destruction of tight junctions and loss of cell-to-cell adhesion causing tumor progression , however the clinical significance in gastric carcinogenesis is more complex. There is evidence that several of the claudins, CLDN1 included, show increasing levels as gastric epithelium progresses to intestinal metaplasia and early gastric carcinoma . CLDN1 might influence intracellular signalling, demonstrated by Liu et al. who showed that elevated expression of CLDN1 in breast cancer cells contributed to an anti-apoptotic effect through two mechanisms: inhibition of caspase-8 cleavage, and activation of the Wnt/β-catenin signal pathway . CLDN1 has been identified within the nucleus of gastric cancer AGS cells in vitro, suggesting a regulatory role of CLDN1 on cell proliferation, migration and invasiveness at a nuclear level . Some studies on ovarian and colon cancer report a role of CLDN1 on metastatic processes through activation of metalloproteinases, reducing apoptosis and increasing migration . Although there are several papers to support an oncogenic role of CLDN1 in gastric cancer, two studies nevertheless showed reduced CLDN1 staining in metastatic compared to non-metastatic gastric cancer , and increased tumorgenicity in CLDN1 negative gastric epithelial cells , contrasting our findings.
The expression pattern of CLDN1 differs not only between different stages of carcinogenesis, but also between histological subtypes and between regions of the gastrointestinal tract. Resnick et al. demonstrated increased staining of CLDN1 protein in intestinal compared to diffuse type gastric cancer . In contrast, Jung et al. demonstrated significantly lower CLDN1 expression in intestinal compared to diffuse type . Neither studies found any correlation between CLDN1 and prognosis. Wu et al. demonstrated positive correlation between CLDN1 expression and invasiveness and metastasis in gastric tumors using immunohistochemistry . In two studies on colorectal cancer, low expression of CLDN1 was a predictor of poor prognosis [40, 41], however an association between high CLDN1 expression and depth of tumor invasion was also noted . In summary, the role of CLDN1 in cancer progression and prognosis is far from clear.
Our data demonstrate a marked increase in CLDN1 expression in 19 of 20 tumors compared to normal tissue, with a significant and independent relationship between high CLDN1 expressing tumors and reduced postoperative survival. We found no statistically significant difference between CLDN1 expression and histological subtypes, for that our sample number is insufficient. Nevertheless, tumors with high CLDN1 expression (FC > 2.14) showed an extremely poor prognosis as there were no patients alive at 450 days following curatively intended surgery in this group. In the low-expressing CLDN1 group (FC < 2.14), patients showed significantly longer post-operative survival, and 50% of the patients were still alive at the end of the study. We have reported total mortality and not cancer specific mortality. Our sample number is small, and a much larger study would be required to reveal statistically significant correlation between CLDN1 expression and sample subgroups, such as the histological subtypes, different tumor stages and H. pylori status. The role of CLDN1 in gastrointestinal cancer is controversial, but it seems convincing that the high CLDN1 gene expression conferred a very unfavorable prognosis in our study population. Moreover, CLDN1 was also one of the most significantly up-regulated genes in the previously studied H. pylori-exposed gastric epithelial cells , suggesting a possible causal relationship between chronic H. pylori exposure and CLDN1 up-regulation in gastric mucosa.
Other claudins that were up-regulated in the tumor samples were CLDN2 and CLDN7, and these genes might also be implicated in gastric carcinogenesis [36, 42–48]. CLDN7 was also among the most significantly up-regulated gene in the H. pylori exposed gastric epithelial cells , suggesting a role of this bactierium in the regulation of this gene.
The most consistently increased gene in the study was IL-8, up-regulated in the tumor in 18 of 20 tissue pairs. IL-8 is one of the major mediators of inflammation and a powerful chemokine that targets neutrophils and lymphocytes through the receptors CXCR1 and CXCR2. IL-8 is paramount in the acute inflammatory response to H. pylori infection and is also increased in chronic gastritis . The increased IL-8 expression in the tumor samples may represent intratumoral inflammation as a normal reaction to an abnormal environment. However, the absence of other acute or chronic inflammatory genes suggests that the up-regulated IL-8 in the tumors can not be entirely explained by an inflammatory process alone. Hence, the role of IL-8 in the gastric cancer is not clear. First, persistent and chronic inflammation in the stomach is associated with an enhanced production of several pro-inflammatory cytokines including IL-8 which increases apoptosis, hyperproliferation and production of reactive oxygen and nitrogen species causing DNA damage and mutations. Second, increased vascularization is one of the hallmarks of malignant transformation, and IL-8 may serve an important role in this process. Several authors have demonstrated promotion of angiogenesis in tissue exposed to IL-8 protein [51–53]. A plausible causal role of IL-8 in the growth and vascularization of gastric cancer has also been shown in the work of Kitadai et al., where IL-8 transfected cells that were injected into the gastric wall of mice, rapidly produced growth of highly vascularized tumors . Interestingly, we also found significantly increased and coordinated up-regulation of COL1A1 and COL1A2 in the tumor tissue, both of which are important in blood vessel development. Two authors recently found an association between IL-8 and adhesion, migration, and invasion in gastric cancer cells [55, 56]. Targeting of the IL-8 receptor CXCR2 has been suggested as a novel cancer treatment in several studies [53, 55–57].
In our previous study we identified IL-8 as the single most up-regulated gene in the acute response of gastric epithelial cells exposed to H. pylori in vitro. IL-8 is also up-regulated in the pre-malignant stages of gastric cancer, such as chronic gastritis  and intestinal metaplasia . With IL-8 being currently demonstrated as the single most up-regulated gene in surgically resected GC tumors, the up-regulation of this gene throughout gastric cancer progression may constitute an early and important event in the disease, initiated and maintained by H. pylori infection.
The causal relationship between H. pylori colonization of the stomach and GC has been widely accepted . In this study only 2 of the 20 gastric tumors showed active H. pylori infection at the time of surgery, 1 intestinal and 1 diffuse type cancer. While more than 90% of the GC reported in Asian countries are considered attributable to this bacterium , our findings might indicate a lesser role of H. pylori in gastric cancer in a country like Norway. However, GC tissue is frequently H. pylori negative, due to the mucosal atrophy caused by the bacteria itself. While H. pylori colonization drives forward the progression of mucosal atrophy and intestinal metaplasia, this process paradoxically also slowly eradicates the same bacteria from the gastric mucosa which causes a decrease in active inflammation .
In the current study, we demonstrated up-regulation of several matrix metalloproteinases (MMPs); and KRT17 in the tumor of almost all the tissue pairs. MMPs participate in the degradation of extracellular matrix and the regulation of tumor growth and angiogenesis, and are important in the detachment of malignant cells from adjacent tissue to attain metastatic ability. Keratin 17 has been shown to be over-expressed in several adenocarcinomas including GC, and an association with aggressive tumor behaviour, local invasion, metastasis as well as treatment responsiveness has also been suggested [63–65]. We found no assiciation between MMPS and KRT17 and clinicopathological parameters. However, other studies have demonstrated an association with MMPs and advanced tumor stage, high grade tumors and metastasis, as well as a role for MMP11 as a serum marker in GC disease [66–69]. MMP7 and KRT17 were also among the most up-regulated genes our previous study of gastric epithelial cells exposed to H. pylori, which raises the possibility of a role of H. pylori also in the regulation of these genes.
In hiarchical clustering of the samples, the tumor and the control tissues clustered separately. Normal mucosa tissue bore a closer biological resemblance to normal mucosa from the other individuals, than to the tumor counterpart from its own stomach. In similar fashion, most tumor samples clustered together, demonstrating common genetic features between the tumor specimens. In addition, there was a large horizontal distance between the tumor specimen and the normal specimen within each tissue pair, illustrating that a significant shift in gene expression has occurred during the progression from normal mucosa to cancer within the same stomach. Furthermore, the mixed type and the intestinal type of cancers formed two almost exclusive clusters compared to the diffuse type cancers, indicating that each of the histological types have distinct gene expression profiles. Surprisingly, the mixed type cluster showed the greatest difference in gene expression compared to the normal tissue, indicating that the biology of this type of GC has removed itself the most from the original naive tissue. The results are interesting, but the sample number is too small to draw any conclusions.
We performed GO analyses to cluster the most differentially regulated genes according to biological function. Several terms relating to cell adhesion were enriched by genes up-regulated in the tumor samples. KEGG pathway analysis also showed that a number of pathways regulating cell attachment were significantly affected, in agreement with the GO analysis. Disruption of primary cell attachments, and secondly, cell adhesion to distant sites, are two fundamental steps in the ability of tumor cells to develop metastatic disease. Blood vessel development is essential for the tumor’s ability to survive and metastasize to distant sites. This gain of abilities seems to come at the cost of loss of features of differentiated intestinal tissue, such as digestive and excretive processes, which were associated with down-regulated genes. While several of the highly up-regulated genes were mapped to important pathways, none of the 100 down-regulated genes were involved in any significant pathways, indicating that it is the net gain of oncological function that translates into tumor growth and malignant behavior, rather than the loss of tumor suppression.
In our study, CLDN1 was not only highly up-regulated in the gastric cancer samples, but CLDN1 expression was also independently associated with a very poor post-operative prognosis. IL-8 was the single most up-regulated gene in the study, and we have shed new light on the role of both genes in gastric carcinogenesis. IL-8 and CLDN1 may represent important links between GC and the gene response seen in acute H. pylori infection of gastric epithelial cells. Intestinal, diffuse and mixed type of gastric cancer formed separate gene expression clusters, but also showed many genetic similarities. Functional analysis demonstrated that several cellular pathways regulating cell attachment were affected in the tumor tissue.
The Illumina service was provided by the Norwegian Microarray Consortium (NMC) at the national technology platform, and supported by the functional genomics program (FUGE) in the Research Council of Norway. The University of Oslo financed the project. Thanks to Armand Borovik at the Prince of Wales Hospital, Sydney, Australia, for valuable comments.
- Cancer registery of Norway: Cancer in Norway 2010, Cancer incidence, mortality, survival and prevalence in Norway. 2013, Oslo, Norway: Cancer Registry of NorwayGoogle Scholar
- Ferlay J, Shin HR, Bray F, Forman D, Mathers C, Parkin DM: GLOBOCAN 2008 v2.0, Cancer Incidence and Mortality Worldwide: IARC CancerBase No. 10. Lyon. 2010, France: International Agency for Research on Cancer, http://globocan.iarc.fr,Google Scholar
- Takeno A, Takemasa I, Seno S, Yamasaki M, Motoori M, Miyata H, et al: Gene expression profile prospectively predicts peritoneal relapse after curative surgery of gastric cancer. Ann Surg Oncol. 2010, 17: 1033-1042. 10.1245/s10434-009-0854-1.View ArticlePubMedGoogle Scholar
- Teramoto K, Tada M, Tamoto E, Abe M, Kawakami A, Komuro K, et al: Prediction of lymphatic invasion/lymph node metastasis, recurrence, and survival in patients with gastric cancer by cDNA array-based expression profiling. J Surg Res. 2005, 124: 225-236. 10.1016/j.jss.2004.10.003.View ArticlePubMedGoogle Scholar
- Chen CN, Lin JJ, Chen JJ, Lee PH, Yang CY, Kuo ML, et al: Gene expression profile predicts patient survival of gastric cancer after surgical resection. J Clin Oncol. 2005, 23: 7286-7295. 10.1200/JCO.2004.00.2253.View ArticlePubMedGoogle Scholar
- Motoori M, Takemasa I, Doki Y, Saito S, Miyata H, Takiguchi S, et al: Prediction of peritoneal metastasis in advanced gastric cancer by gene expression profiling of the primary site. Eur J Cancer. 2006, 42: 1897-1903. 10.1016/j.ejca.2006.04.007.View ArticlePubMedGoogle Scholar
- Motoori M, Takemasa I, Yano M, Saito S, Miyata H, Takiguchi S, et al: Prediction of recurrence in advanced gastric cancer patients after curative resection by gene expression profiling. Int J Cancer. 2005, 114: 963-968. 10.1002/ijc.20808.View ArticlePubMedGoogle Scholar
- Cho JY, Lim JY, Cheong JH, Park YY, Yoon SL, Kim SM, et al: Gene expression signature-based prognostic risk score in gastric cancer. Clin Cancer Res. 2011, 17: 1850-1857. 10.1158/1078-0432.CCR-10-2180.View ArticlePubMedPubMed CentralGoogle Scholar
- Lauren P: The two histological main types of gastric carcinoma: Diffuse and so-called intestinal-type carcinoma. An attempt at a histo-clinical classification. Acta Pathol Microbiol Scand. 1965, 64: 31-49.PubMedGoogle Scholar
- Correa P, Piazuelo MB: The gastric precancerous cascade. J Dig Dis. 2012, 13: 2-9. 10.1111/j.1751-2980.2011.00550.x.View ArticlePubMedPubMed CentralGoogle Scholar
- Zabaleta J: Multifactorial etiology of gastric cancer. Methods Mol Biol. 2012, 863: 411-435. 10.1007/978-1-61779-612-8_26.View ArticlePubMedPubMed CentralGoogle Scholar
- Hudler P: Genetic aspects of gastric cancer instability. Sci World J. 2012, 2012: 761909-View ArticleGoogle Scholar
- Nagini S: Carcinoma of the stomach: a review of epidemiology, pathogenesis, molecular genetics and chemoprevention. World J Gastrointest Oncol. 2012, 4: 156-169. 10.4251/wjgo.v4.i7.156.View ArticlePubMedPubMed CentralGoogle Scholar
- Zheng HC, Li XH, Hara T, Masuda S, Yang XH, Guan YF, et al: Mixed-type gastric carcinomas exhibit more aggressive features and indicate the histogenesis of carcinomas. Virchows Arch. 2008, 452: 525-534. 10.1007/s00428-007-0572-7.View ArticlePubMedPubMed CentralGoogle Scholar
- Yang X, Takano Y, Zheng HC: The pathobiological features of gastrointestinal cancers (Review). Oncol Lett. 2012, 3: 961-969.PubMedPubMed CentralGoogle Scholar
- Tan IB, Ng I, Tai WM, Tan P: Understanding the genetic basis of gastric cancer: Recent advances. Expert Rev Gastroenterol Hepatol. 2012, 6: 335-341. 10.1586/egh.12.7.View ArticlePubMedGoogle Scholar
- Eftang LL, Esbensen Y, Tannaes TM, Bukholm IR, Bukholm G: Interleukin-8 is the single most up-regulated gene in whole genome profiling of H. pylori exposed gastric epithelial cells. BMC Microbiol. 2012, 12: 9-10.1186/1471-2180-12-9.View ArticlePubMedPubMed CentralGoogle Scholar
- Sipponen P, Price AB: The Sydney System for classification of gastritis 20 years ago. J Gastroenterol Hepatol. 2011, 26 (Suppl 1): 31-34.View ArticlePubMedGoogle Scholar
- Dixon MF, Genta RM, Yardley JH, Correa P: Classification and grading of gastritis. The updated Sydney System. International Workshop on the Histopathology of Gastritis, Houston 1994. Am J Surg Pathol. 1996, 20: 1161-1181.View ArticlePubMedGoogle Scholar
- Illumina I: HumanHT-12 v3 Expression BeadChip data sheet. http://www.illumina.com/Documents/products/datasheets/datasheet_humanht_12.pdf,
- Illumina I: Illumina Annotation Files. http://support.illumina.com/downloads/humanht-12_v3_product_files.ilmn,
- R: Development core team: A language and environment for statistical computing. 2008, Vienna, Austria: R Foundation for Statistical ComputingGoogle Scholar
- Gentleman RC, Carey VJ, Bates DM, Bolstad B, Dettling M, Dudoit S, et al: Bioconductor: open software development for computational biology and bioinformatics. Genome Biol. 2004, 5: R80-10.1186/gb-2004-5-10-r80.View ArticlePubMedPubMed CentralGoogle Scholar
- Dunning MJ, Barbosa-Morais NL, Lynch AG, Tavare S, Ritchie ME: Statistical issues in the analysis of Illumina data. BMC Bioinformatics. 2008, 9: 85-10.1186/1471-2105-9-85.View ArticlePubMedPubMed CentralGoogle Scholar
- Cairns JM, Dunning MJ, Ritchie ME, Russell R, Lynch AG: BASH: a tool for managing BeadArray spatial artefacts. Bioinformatics. 2008, 24: 2921-2922. 10.1093/bioinformatics/btn557.View ArticlePubMedPubMed CentralGoogle Scholar
- Stavrum AK, Petersen K, Jonassen I, Dysvik B: Analysis of gene-expression data using J-Express. Curr Protoc Bioinformatics. 2008, Chapter 7: Unit 7.3Google Scholar
- Breitling R, Armengaud P, Amtmann A, Herzyk P: Rank products: a simple, yet powerful, new method to detect differentially regulated genes in replicated microarray experiments. FEBS Lett. 2004, 573: 83-92. 10.1016/j.febslet.2004.07.055.View ArticlePubMedGoogle Scholar
- 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: 3775-3781. 10.1093/nar/gkg624.View ArticlePubMedPubMed CentralGoogle Scholar
- Draghici S, Khatri P, Tarca AL, Amin K, Done A, Voichita C, et al: A systems biology approach for pathway level analysis. Genome Res. 2007, 17: 1537-1545. 10.1101/gr.6202607.View ArticlePubMedPubMed CentralGoogle Scholar
- Kanehisa M, Goto S: KEGG: kyoto encyclopedia of genes and genomes. Nucleic Acids Res. 2000, 28: 27-30. 10.1093/nar/28.1.27.View ArticlePubMedPubMed CentralGoogle Scholar
- Khatri P, Sellamuthu S, Malhotra P, Amin K, Done A, Draghici S: Recent additions and improvements to the Onto-Tools. Nucleic Acids Res. 2005, 33: W762-W765. 10.1093/nar/gki472.View ArticlePubMedPubMed CentralGoogle Scholar
- ArrayExpress EMBL-EBI - functional genomics data. http://www.ebi.ac.uk/arrayexpress/,
- Jung H, Jun KH, Jung JH, Chin HM, Park WB: The expression of claudin-1, claudin-2, claudin-3, and claudin-4 in gastric cancer tissue. J Surg Res. 2011, 167: e185-e191. 10.1016/j.jss.2010.02.010.View ArticlePubMedGoogle Scholar
- Iravani O, Tay BW, Chua PJ, Yip GW, Bay BH: Claudins and gastric carcinogenesis. Exp Biol Med (Maywood). 2013, 238: 344-349. 10.1177/1535370213477981.View ArticleGoogle Scholar
- Liu Y, Wang L, Lin XY, Wang J, Yu JH, Miao Y, et al: Anti-apoptotic effect of claudin-1 on TNF-alpha-induced apoptosis in human breast cancer MCF-7 cells. Tumour Biol. 2012, 33: 2307-2315. 10.1007/s13277-012-0493-1.View ArticlePubMedGoogle Scholar
- Zavala-Zendejas VE, Torres-Martinez AC, Salas-Morales B, Fortoul TI, Montano LF, Rendon-Huerta EP: Claudin-6, 7, or 9 overexpression in the human gastric adenocarcinoma cell line AGS increases its invasiveness, migration, and proliferation rate. Cancer Invest. 2011, 29: 1-11. 10.3109/07357907.2010.512594.View ArticlePubMedGoogle Scholar
- Chang TL, Ito K, Ko TK, Liu Q, Salto-Tellez M, Yeoh KG, et al: Claudin-1 has tumor suppressive activity and is a direct target of RUNX3 in gastric epithelial cells. Gastroenterology. 2010, 138: 255-265. 10.1053/j.gastro.2009.08.044.View ArticlePubMedGoogle Scholar
- Resnick MB, Gavilanez M, Newton E, Konkin T, Bhattacharya B, Britt DE, et al: Claudin expression in gastric adenocarcinomas: a tissue microarray study with prognostic correlation. Hum Pathol. 2005, 36: 886-892. 10.1016/j.humpath.2005.05.019.View ArticlePubMedGoogle Scholar
- Wu YL, Zhang S, Wang GR, Chen YP: Expression transformation of claudin-1 in the process of gastric adenocarcinoma invasion. World J Gastroenterol. 2008, 14: 4943-4948. 10.3748/wjg.14.4943.View ArticlePubMedPubMed CentralGoogle Scholar
- Shibutani M, Noda E, Maeda K, Nagahara H, Ohtani H, Hirakawa K: Low expression of claudin-1 and presence of poorly-differentiated tumor clusters correlate with poor prognosis in colorectal cancer. Anticancer Res. 2013, 33: 3301-3306.PubMedGoogle Scholar
- Nakagawa S, Miyoshi N, Ishii H, Mimori K, Tanaka F, Sekimoto M, et al: Expression of CLDN1 in colorectal cancer: a novel marker for prognosis. Int J Oncol. 2011, 39: 791-796.PubMedGoogle Scholar
- Song X, Li X, Tang Y, Chen H, Wong B, Wang J, et al: Expression of claudin-2 in the multistage process of gastric carcinogenesis. Histol Histopathol. 2008, 23: 673-682.PubMedGoogle Scholar
- Amasheh S, Meiri N, Gitter AH, Schoneberg T, Mankertz J, Schulzke JD, et al: Claudin-2 expression induces cation-selective channels in tight junctions of epithelial cells. J Cell Sci. 2002, 115: 4969-4976. 10.1242/jcs.00165.View ArticlePubMedGoogle Scholar
- Furuse M, Furuse K, Sasaki H, Tsukita S: Conversion of zonulae occludentes from tight to leaky strand type by introducing claudin-2 into Madin-Darby canine kidney I cells. J Cell Biol. 2001, 153: 263-272. 10.1083/jcb.153.2.263.View ArticlePubMedPubMed CentralGoogle Scholar
- Mima S, Takehara M, Takada H, Nishimura T, Hoshino T, Mizushima T: NSAIDs suppress the expression of claudin-2 to promote invasion activity of cancer cells. Carcinogenesis. 2008, 29: 1994-2000. 10.1093/carcin/bgn134.View ArticlePubMedGoogle Scholar
- Rendon-Huerta E, Teresa F, Teresa GM, Xochitl GS, Georgina AF, Veronica ZZ, et al: Distribution and expression pattern of claudins 6, 7, and 9 in diffuse- and intestinal-type gastric adenocarcinomas. J Gastrointest Cancer. 2010, 41: 52-59. 10.1007/s12029-009-9110-y.View ArticlePubMedGoogle Scholar
- Park JY, Park KH, Oh TY, Hong SP, Jeon TJ, Kim CH, et al: Up-regulated claudin 7 expression in intestinal-type gastric carcinoma. Oncol Rep. 2007, 18: 377-382.PubMedGoogle Scholar
- Johnson AH, Frierson HF, Zaika A, Powell SM, Roche J, Crowe S, et al: Expression of tight-junction protein claudin-7 is an early event in gastric tumorigenesis. Am J Pathol. 2005, 167: 577-584. 10.1016/S0002-9440(10)62999-9.View ArticlePubMedPubMed CentralGoogle Scholar
- Xuan J, Deguchi R, Yanagi H, Ozawa H, Urano T, Ogawa Y, et al: Relationship between gastric mucosal IL-8 levels and histological gastritis in patients with Helicobacter pylori infection. Tokai J Exp Clin Med. 2005, 30: 83-88.PubMedGoogle Scholar
- Chiba T, Marusawa H, Seno H, Watanabe N: Mechanism for gastric cancer development by Helicobacter pylori infection. J Gastroenterol Hepatol. 2008, 23: 1175-1181. 10.1111/j.1440-1746.2008.05472.x.View ArticlePubMedGoogle Scholar
- Koch AE, Polverini PJ, Kunkel SL, Harlow LA, DiPietro LA, Elner VM, et al: Interleukin-8 as a macrophage-derived mediator of angiogenesis. Science. 1992, 258: 1798-1801. 10.1126/science.1281554.View ArticlePubMedGoogle Scholar
- Hu DE, Hori Y, Fan TP: Interleukin-8 stimulates angiogenesis in rats. Inflammation. 1993, 17: 135-143. 10.1007/BF00916100.View ArticlePubMedGoogle Scholar
- Heidemann J, Ogawa H, Dwinell MB, Rafiee P, Maaser C, Gockel HR, et al: Angiogenic effects of interleukin 8 (CXCL8) in human intestinal microvascular endothelial cells are mediated by CXCR2. J Biol Chem. 2003, 278: 8508-8515. 10.1074/jbc.M208231200.View ArticlePubMedGoogle Scholar
- Kitadai Y, Takahashi Y, Haruma K, Naka K, Sumii K, Yokozaki H, et al: Transfection of interleukin-8 increases angiogenesis and tumorigenesis of human gastric carcinoma cells in nude mice. Br J Cancer. 1999, 81: 647-653. 10.1038/sj.bjc.6690742.View ArticlePubMedPubMed CentralGoogle Scholar
- Kuai WX, Wang Q, Yang XZ, Zhao Y, Yu R, Tang XJ: Interleukin-8 associates with adhesion, migration, invasion and chemosensitivity of human gastric cancer cells. World J Gastroenterol. 2012, 18: 979-985. 10.3748/wjg.v18.i9.979.View ArticlePubMedPubMed CentralGoogle Scholar
- Ju D, Sun D, Xiu L, Meng X, Zhang C, Wei P: Interleukin-8 is associated with adhesion, migration and invasion in human gastric cancer SCG-7901 cells. Med Oncol. 2012, 29: 91-99. 10.1007/s12032-010-9780-0.View ArticlePubMedGoogle Scholar
- Schraufstatter IU, Chung J, Burger M: IL-8 activates endothelial cell CXCR1 and CXCR2 through Rho and Rac signaling pathways. Am J Physiol Lung Cell Mol Physiol. 2001, 280: L1094-L1103.PubMedGoogle Scholar
- Bartchewsky W, Martini MR, Masiero M, Squassoni AC, Alvarez MC, Ladeira MS, et al: Effect of Helicobacter pylori infection on IL-8, IL-1beta and COX-2 expression in patients with chronic gastritis and gastric cancer. Scand J Gastroenterol. 2009, 44: 153-161. 10.1080/00365520802530853.View ArticlePubMedGoogle Scholar
- Noshiro M, Kusugami K, Sakai T, Imada A, Ando T, Ina K, et al: Gastric metaplasia in the duodenal bulb shows increased mucosal interleukin-8 activity in Helicobacter pylori-positive duodenal ulcer patients. Scand J Gastroenterol. 2000, 35: 482-489. 10.1080/003655200750023732.View ArticlePubMedGoogle Scholar
- IARC Working Group on the Evaluation of Carcinogenic Risks to Humans. Lyon: Schistosomes, liver flukes and Helicobacter pylori. IARC Monogr Eval Carcinog Risks Hum. 1994, 61: 1-241.Google Scholar
- Kato S, Matsukura N, Tsukada K, Matsuda N, Mizoshita T, Tsukamoto T, et al: Helicobacter pylori infection-negative gastric cancer in Japanese hospital patients: incidence and pathological characteristics. Cancer Sci. 2007, 98: 790-794. 10.1111/j.1349-7006.2007.00478.x.View ArticlePubMedGoogle Scholar
- Kang HY, Kim N, Park YS, Hwang JH, Kim JW, Jeong SH, et al: Progression of atrophic gastritis and intestinal metaplasia drives Helicobacter pylori out of the gastric mucosa. Dig Dis Sci. 2006, 51: 2310-2315. 10.1007/s10620-006-9276-0.View ArticlePubMedGoogle Scholar
- Economescu MC, Necula LG, Dragu D, Badea L, Dima SO, Tudor S, et al: Identification of potential biomarkers for early and advanced gastric adenocarcinoma detection. Hepatogastroenterology. 2010, 57: 1453-1464.Google Scholar
- Su CQ, Qiu H, Zhang Y: Localization of keratin mRNA and collagen I mRNA in gastric cancer by in situ hybridization and hybridization electron microscopy. World J Gastroenterol. 1999, 5: 527-530.View ArticlePubMedPubMed CentralGoogle Scholar
- Pluciennik E, Krol M, Nowakowska M, Kusinska R, Potemski P, Kordek R, et al: Breast cancer relapse prediction based on multi-gene RT-PCR algorithm. Med Sci Monit. 2010, 16: CR132-CR136.PubMedGoogle Scholar
- Miyata Y, Iwata T, Maruta S, Kanda S, Nishikido M, Koga S, et al: Expression of matrix metalloproteinase-10 in renal cell carcinoma and its prognostic role. Eur Urol. 2007, 52: 791-797. 10.1016/j.eururo.2006.12.028.View ArticlePubMedGoogle Scholar
- Zhao ZS, Chu YQ, Ye ZY, Wang YY, Tao HQ: Overexpression of matrix metalloproteinase 11 in human gastric carcinoma and its clinicopathologic significance. Hum Pathol. 2010, 41: 686-696. 10.1016/j.humpath.2009.10.010.View ArticlePubMedGoogle Scholar
- Yang YH, Deng H, Li WM, Zhang QY, Hu XT, Xiao B, et al: Identification of matrix metalloproteinase 11 as a predictive tumor marker in serum based on gene expression profiling. Clin Cancer Res. 2008, 14: 74-81. 10.1158/1078-0432.CCR-07-1179.View ArticlePubMedGoogle Scholar
- Yamashita K, Azumano I, Mai M, Okada Y: Expression and tissue localization of matrix metalloproteinase 7 (matrilysin) in human gastric carcinomas. Implications for vessel invasion and metastasis. Int J Cancer. 1998, 79: 187-194. 10.1002/(SICI)1097-0215(19980417)79:2<187::AID-IJC15>3.0.CO;2-7.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/13/586/prepub
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