Research Article | Open Access
Association between Genetic Instability and Helicobacter pylori Infection in Gastric Epithelial Dysplasia
Background. In gastric carcinogenesis, changes of DNA methylation appear to be an early molecular event, and the genome-wide methylation state is closely correlated with the level of long interspersed nucleotide element-1 (LINE-1) methylation. In this study, we measured LINE-1 methylation level according to genetic instability and evaluated the effect of Helicobacter pylori infection on genetic instability in gastric epithelial dysplasia. Methods. Total 100 tissue samples of gastric epithelial dysplasia were analyzed. Seven loci that linked to tumor suppressor genes were used to identify significant structural chromosomal aberrations. Microsatellite status was investigated for two different microsatellite marker loci (BAT25 and BAT26). Also, we measured LINE-1 methylation level by combined bisulfite restriction analysis (COBRA-LINE-1) method. Results. There were no significant differences of LINE-1 methylation level according to chromosomal/microsatellite instability and H. pylori state. In the dysplastic lesions with H. pylori infection, LINE-1 methylation level of MSI lesion was significantly lower than that of microsatellite stable (MSS) lesion ( versus %, ). Conclusions. In gastric epithelial dysplasia with H. pylori infection, MSI is correlated with reduced LINE-1 methylation level. Coexistence of H. pylori infection and MSI might be a driving force of gastric carcinogenesis.
Epidemiological studies in the last decade have established a strong causal relationship between Helicobacter pylori (H. pylori) infection and gastric cancer, and this bacteria has been classified as a Group I carcinogen by the World Health Organization (WHO) [1–3]. Previously, Correa suggested a human model of gastric carcinogenesis, and he postulated that the development of gastric cancer starts from chronic gastritis to gastric atrophy, intestinal metaplasia, dysplasia, and finally invasive cancer . H. pylori infection stimulates cell proliferation in the gastric epithelium and induces apoptosis. It results in imbalance between apoptosis and proliferation and produces alterations or mutations of genes [5, 6]. Eventually, it increases the risk of developing gastric cancer. In the view of this point, the eradication therapy of H. pylori would be an attractive therapeutic modality, but it does not prevent the development of gastric cancer in all patients [7, 8]. Researchers are needed to further elucidate how H. pylori infection increases the risk of gastric cancer.
In cancer cell, abnormal DNA methylation is characterized by bidirectional changes—regional CpG island hypermethylation and generalized genomic hypomethylation. Both kinds of changes are observed simultaneously, but these two changes are not reciprocal. They might be independent events . Several studies suggest that genome-wide hypomethylation generally arises earlier, whereas hypermethylation occurs in promoters and is usually a later event. Therefore, global DNA hypomethylation is considered as the hallmark of cancer because the genes vulnerable to aberrant hypermethylation usually are overlapped by the genes targeted by hypomethylation [10–12]. In gastric cancer, global DNA hypomethylation is frequently observed at the very early stage of carcinogenesis [13, 14]. LINE (long interspersed nucleotide element)-1, a highly repeated interspersed human retrotransposon, is ubiquitous and constitutes approximately 17% of the human genome. The level of LINE-1 methylation reflects the genome-wide methylation level, and the reduced level is responsible for the overall losses of DNA methylation. Also, it means regional hypermethylation of specific genes. In gastric carcinogenesis, the levels of LINE-1 methylation decrease from the chronic gastritis to gastric cancer stages, regardless of the status of H. pylori infection [15–18].
In this study, we measure LINE-1 methylation level according to chromosomal/microsatellite instability and H. pylori status in gastric premalignant lesion. We aim to elucidate mechanisms on how H. pylori infection triggers the progression of gastric premalignant lesion to true gastric cancer.
2. Materials and Methods
All tissues were excised by therapeutic endoscopic mucosal resection. The diagnosis of tissue sample was confirmed by two different histopathologists according to the revised Vienna classification; when they disagreed, the tissue sample was excluded from the study. All normal tissues had grossly intact mucosa and were at least 1 cm from the mucosal lesion; they were obtained by gastric biopsy just after an endoscopic mucosal resection. The H. pylori status was evaluated according to the histological results (silver stain or CLO test). In the present study, two biopsies were taken both from antrum and corpus after 4 weeks of the endoscopic resection for evaluation of H. pylori infection.
2.1. DNA Extraction and Assessment of Loss of Heterozygosity (LOH)
Four-micrometer-thick tissue sections from the dysplasia/cancer and normal tissues were placed on a glass slide and stained with hematoxylin and eosin. The diagnosis of the tissue samples was confirmed by two different histopathologists. Prior to DNA extraction, all the tumor sites were checked for the tumor cell contents ≥70% using a stereomicroscope under a ×40 magnification. To deparaffinize, we utilized a standard series of washes in xylenes and alcohol. Using a 30-gauge needle and a pointed surgical blade, the pathologist performed the microdissection while looking through the microscope. Tissue fragments were deposited into the collection tube.
LOH was analyzed as described previously [19, 20]. After DNA extraction by standard method, seven loci that linked to tumor suppressor genes were used to identify significant structural chromosomal aberrations. The DNA was amplified by PCR at loci linked to the adenomatous polyposis coli (APC) locus at 5q21 (D5S505), possible tumor suppressor/senescence gene locus at 10p15 (D10S501 and D10S602), the p53 locus at 17p13 (TP53), the BRCA1 locus at 17q21 (D17S855), and the DCC locus at 18q21 (D18S58 and D18S61).
In brief, 4 mL 30% acrylamide (29 : 1) solution, 2.4 mL 5 × TBE solution, 5.6 mL ddH2O, 200 μL 10% ammonium persulfate, and 10 μL TEMED were blended adequately and poured into the gel then concreted for 1 hour at room temperature. Ten μL of PCR product and 2 μL of loading buffer (95% formamide, 10 mM NaOH, 0.1% bromophenol blue, 0.1% xylene cyanol) were mixed. The mixture was centrifuged for 15 seconds, denatured at 93°C for 3 minutes, bathed in ice for 10 minutes, placed onto a 10% nondenaturation polyacrylamide gel, and separated with 0.5 × TBE buffer for 2 hours at RT and 100 V.
After electrophoresis, the gel was stained using the Bio-Rad Silver Stain kit (Bio-Rad, Philadelphia, PA, USA). Briefly, the gel was fixed with 40% methanol for 30 minutes, oxidized for 5 minutes, rinsed for 5 minutes three times, silver stained for 20 minutes, rinsed for 30 seconds, developed for 1 minute three times, and stopped with 5% acetic acid for 15 minutes. The staining results were analyzed with Gel DocXR (Bio-Rad). Assessment of loss of heterozygosity (LOH) was assigned when a tumor allele showed at least 50% gain or reduction in the relative intensity (Figure 1).
2.2. Assessment of Microsatellite Instability (MSI)
DNA samples were amplified using two different oligonucleotide pairs specific for the recommended microsatellite loci BAT25 and BAT26. Primer sequences (Integrated DNA Technologies, Iowa, USA) were: BAT25 (forward 59-TCGCCTCCAAGAATGTAA GT-39 and reverse 59-TCTGCATTTTAACTATGGCTC-39), and BAT26 (forward 59-TGACTACTTTTGACTTCAGCC-39 and reverse 59-ACCATTCAACATTTTTAACCC-39). PCR reactions were performed as described previously. PCR products were run on 8% denaturing polyacrylamide gels at 180 V for 18 hours, and visualized by silver staining (Figure 1).
2.3. Assessment of LINE-1 Methylation Status
A modified long interspersed nucleotide elements-combined bisulfite restriction analysis (COBRA LINE-1) method was used to analyze LINE-1 methylation status of the cancers [17, 21, 22]. This method is based on the principle that cytosine in DNA is converted to uracil when DNA is treated with sodium bisulfite, whereas methylated cytosine is protected from the conversion. Thus, the methylated and unmethylated cytosine could be distinguished by digestion with a restriction enzyme that recognizes sequences containing CpG. The extracted DNA was treated with sodium bisulfite and isolated using the EZ DNA methylation kit (Zymo Research, Orange, CA, USA). Bisulfite-treated DNA was amplified by 40 cycles of PCR with two primers, LINE 3 (5V-GYGTAAGGGGTTAGGGAGTTTTT) and LINE 4 (5V-AACRTAAAACCCTCCRAACCAAATATAAA), at an annealing temperature of 50°C. The PCR products were digested with the TaqI restriction enzyme, which recognizes TCGA, for 1 hour at 65°C, and then were separated by electrophoresis on 2% agarose gels. The densities of the digested and undigested bands were obtained by scanning with Gel Doc XR (Bio-Rad, Philadelphia, USA) and scoring with Quantity One Software (Bio-Rad, Philadelphia, USA). The ratio of the digested fragments (80 bp) derived from the methylated DNA divided by the sum of the digested fragments and the undigested fragments (160 bp) derived from the unmethylated DNA represents the fractional methylation (expressed as a percentage) at the LINE TaqI site (Figure 2).
2.4. Statistical Analysis
For the quantitative variables, the mean and its standard deviation were calculated. For the qualitative variables, the percent and its 95% confidence interval (95% CI) were calculated. We used the χ2 test to analyze the association between the H. pylori status and other baseline characteristics. For comparison of age and the level of LINE-1 methylation we used the unpaired t test. We used the SPSS statistical package (version 12.0.1) for all analyses.
Total 100 tissue samples (from 61 men, mean age years; 39 women, mean age years) were examined and analyzed. When the gastric epithelial dysplasia (GED) was divided according to the revised Vienna classification, 50 tissues were low-grade (category 3) and 50 were high-grade dysplasia or intramucosal cancer (category 4). Total 54 tissue samples of GED had associated H. pylori infection.
3.1. LOH in Gastric Epithelial Dysplasia
The incidence of LOH was 83% (83/100) in GED, and the frequencies of LOH were 34% on APC (D5S505), 40% on 10p (D10S501), 48% on 10p (D10S602), 14% on p53 (TP 53), 40% on BRCA1 (D17S855), 51% on DCC (D18S58), and 45% on DCC (D18S61), respectively. According to the classification of chromosomal loss described previously, GED was divided into negative (LOH-negative), low-level (LOH-L; 3 or fewer losses), and high level (LOH-H; 4 or more losses). The incidence of LOH-L was 47% (47/100), whereas LOH-H was 36% (36/100). The frequencies of LOH with H. pylori infection were 76.5% (13/17), 48.9% (23/47), and 50.0% (18/36) in LOH-negative, LOH-L, and LOH-H lesion, respectively. There was no significant difference between H. pylori infection and LOH state (). LINE-1 methylation level of lesions with LOH-negative was not significantly different from that of LOH-positive. Also, LINE-1 methylation level of lesions with LOH-L was not significantly different from that of LOH-H (Table 1). Among the lesions with H. pylori infection, LINE-1 methylation level of LOH-L was not different from that of LOH-H (Figure 2).
|LOH: loss of heterozygosity; LOH-L: LOH (+) <3 loci; LOH-H: LOH (+) >4 loci; MSS: microsatellite stable; MSI: microsatellite instable, *statistically significant.|
3.2. MSI in Gastric Epithelial Dysplasia
The frequency of microsatellite instability (MSI) was 36% (36/100), and instability rates for the BAT25 and BAT26 were 19% and 29%, respectively. The frequency of BAT25 (+) with H. pylori infection was 11%, and BAT26 (+) with H. pylori infection was 22%.
LINE-1 methylation level of MSI was not significantly different from that of microsatellite stable (MSS) lesions (Table 1). The frequency of MSI with H. pylori infection was 61.1% (22/36), and it was not different from that of MSS lesion (50.0%, 32/64) (). In the GED with H. pylori infection, LINE-1 methylation level of MSI lesion was significantly lower than that of microsatellite stable (MSS) lesion (, , ) (Figure 3).
3.3. Gastric Epithelial Dysplasia Subgrouped by the Revised Vienna Classification
The tissue samples were divided into two groups according to the revised Vienna classification: low-grade dysplasia (category 3) and high-grade dysplasia/intramucosal cancer (category 4). Twenty six patients with category 3 GED and 28 patients with category 4 GED had associated H. pylori infection (). The category 4 lesion had lower level of LINE-1 methylation than the category 3 lesion ( versus %, respectively, ). For categories 3 and 4, the difference in the frequency of LOH-H was not significant (30.0%, 15/50 versus 42.0%, 21/50; ). The frequencies of MSI positive were 30% and 42.0% (22/51) in categories 3 and 4 (Table 2). In category 3 lesion, LINE-1 methylation level of MSI was significantly lower than that of MSS ( versus %, respectively, ) (Figure 4).
|LOH: loss of heterozygosity; LOH-L: LOH (+) <3 loci; LOH-H: LOH (+) >4 loci; MSS: microsatellite stable; MSI: microsatellite instable, *statistically significant.|
It is widely accepted that gastric cancer develops through the accumulation of genetic or epigenetic alterations affecting oncogenes and tumor suppressor genes. These alterations involve the mechanisms that control genetic instability. Genetic instability is divided into two categories, chromosomal instability (CIN) and microsatellite instability (MSI) and whether the instability is at the chromosomal or nucleotide level in a lesion [23, 24]. CIN has been recognized as the most common feature of sporadic gastric cancers and CIN phenotype has been reported in up to 84% of gastrointestinal tumors , which is compatible with our result. The consequence of CIN is an imbalance in the chromosome number and an increased rate of loss of heterozygosity (LOH). An increased rate of LOH is an important property of CIN, because it accelerates the inactivation of the tumor suppressor genes . In colon cancer model, CIN is an important event in the tumor initiation and progression, and LOH and MSI are inversely correlated . However, in gastric cancer, these are not mutual. In present study, CIN and MSI coincided in 24% of gastric epithelial dysplasia, whereas evidence of both CIN and MSI was lacking in 4%. In the latter cases, it may be associated with the transcriptional silencing of genes by epigenetic alterations.
It is postulated that persistent infection with H. pylori initiates chronic inflammation, which induces increased tissue turnover, increased rate of mutagenesis, and genetic instability. However, several researchers suggested that H. pylori did not exert direct effects in inducing structural chromosomal aberrations and triggering gastric carcinogenesis [28, 29]. In present study, there were no differences of LINE-1 methylation level, irrespective of H. pylori infection and the degree of chromosomal instability (LOH-negative, LOH-L, and LOH-H). It seemed unlikely that H. pylori served as a direct inducer of chromosomal instability. However, we cannot rule out the possibility that some cases were negative for H. pylori at the time of diagnosis of gastric dysplasia but had suffered H. pylori infection previously. The underestimation of the effect of H. pylori on chromosomal instability could exist in this study.
MSI is a molecular phenotype for human cancers with defects in the postreplicative DNA mismatch repair system. H. pylori might promote development of gastric carcinoma at least in part through its ability to affect the DNA mismatch repair system and its deficiency resulted in MSI phenotype [30, 31]. It is known that the frequency of MSI in gastric cancer is between 25% and 50% . MSI-positive gastric cancers have been reported to be located in the distal stomach and associated with intestinal-type histology and favorable clinical features . Despite of association with H. pylori and MSI, there was no difference of LINE-1 methylation level according to microsatellite state or H. pylori infection state in our results. However, in gastric epithelial dysplasia with H. pylori infection, MSI had a tendency of the reduced level of LINE-1 methylation. It suggested that H. pylori might appear as a cofactor for inducing gastric carcinogenesis.
To identify MSI, the five suitable markers including BAT25, BAT26, D2S123, D17S250, and D5S346 have been proposed . Nevertheless, we use only two monomorphic mononucleotides (BAT25 and BAT26) in this study. Although the frequency for MSI-positive was considerably similar with the previous study , the potential pitfall to define MSI existed because of a huge number and diversity of microsatellite regions in the human genome. However, previous studies show that BAT25 and BAT26 are more sensitive and better markers for microsatellite instability detection than their dinucleotide counterparts [34, 35]. These markers are considered to be sensitive in detecting MSI of tumors and can be testable even in the absence of normal tissue.
Gastric low-grade dysplasia can progress into an invasive form, but all cases of it do not transform to advanced carcinoma. It has been reported that approximately 15%–30% of low-grade dysplasia progress to high-grade dysplasia or adenocarcinoma [36–38]. To date, there is no doubt that H. pylori infection is a major risk factor in the pathogenesis of gastric cancer. The curious problem is which factor determines progression of gastric epithelial lesions. Whether H. pylori infection can contribute to the progression of low-grade dysplasia is debatable, and whether the eradication of H. pylori infection would reduce the risk of gastric cancer is also controversial. In this point of view, our results are very hopeful. It supports that progression of gastric epithelial dysplasia to true gastric cancer could be blocked after H. pylori eradication in the selected cases—MSI positive state.
In conclusion, MSI-positive gastric epithelial dysplasia with H. pylori infection is correlated with reduced LINE-1 methylation level. Coexistence of H. pylori infection and MSI might be a driving force of gastric carcinogenesis. To clarify these results, the investigators will conduct a prospective, randomized, and population-based study to determine whether H pylori eradication can reduce the incidence of gastric cancer.
- N. Uemura, S. Okamoto, S. Yamamoto et al., “Helicobacter pylori infection and the development of gastric cancer,” The New England Journal of Medicine, vol. 345, no. 11, pp. 784–789, 2001.
- R. M. Peek Jr. and J. E. Crabtree, “Helicobacter pylori and gastric neoplasia,” The Journal of Pathology, vol. 208, no. 2, pp. 233–248, 2006.
- H. Moller, E. Heseltine, and H. Vainio, “Working group report on schistosomes, liver flukes and Helicobacter pylori,” International Journal of Cancer, vol. 60, no. 5, pp. 587–589, 1995.
- P. Correa and J. Houghton, “Carcinogenesis of Helicobacter pylori,” Gastroenterology, vol. 133, no. 2, pp. 659–672, 2007.
- J. F. R. Kerr, C. M. Winterford, and B. V. Harmon, “Apoptosis: its significance in cancer and cancer therapy,” Cancer, vol. 73, no. 8, pp. 2013–2026, 1994.
- P. Hofman, B. Waidner, V. Hofman, S. Bereswill, P. Brest, and M. Kist, “Pathogenesis of Helicobacter pylori infection,” Helicobacter, vol. 9, supplement 1, no. 1, pp. 15–22, 2004.
- B. C. Wong, S. K. Lam, W. M. Wong et al., “Helicobacter pylori eradication to prevent gastric cancer in a high-risk region of China: a randomized controlled trial,” The Journal of the American Medical Association, vol. 291, no. 2, pp. 187–194, 2004.
- K. Mabe, M. Takahashi, H. Oizumi et al., “Does Helicobacter pylori eradication therapy for peptic ulcer prevent gastric cancer?” World Journal of Gastroenterology, vol. 15, no. 34, pp. 4290–4297, 2009.
- M. Ehrlich, “Cancer-linked DNA hypomethylation and its relationship to hypermethylation,” Current Topics in Microbiology and Immunology, vol. 310, pp. 251–254, 2006.
- N. Gilbert, A. J. Doucet, and A. Bucheton, “Instability associated with human LINE-1 rétrotransposition,” Journal de la Societe de Biologie, vol. 198, no. 4, pp. 419–424, 2004.
- N. Y. Cho, B. H. Kim, M. Choi et al., “Hypermethylation of CpG island loci and hypomethylation of LINE-1 and Alu repeats in prostate adenocarcinoma and their relationship to clinicopathological features,” Journal of Pathology, vol. 211, no. 3, pp. 269–277, 2007.
- A. P. Feinberg, R. Ohlsson, and S. Henikoff, “The epigenetic progenitor origin of human cancer,” Nature Reviews Genetics, vol. 7, no. 1, pp. 21–33, 2006.
- J. Y. Fang and S. D. Xiao, “Alteration of DNA methylation in gastrointestinal carcinogenesis,” Journal of Gastroenterology and Hepatology, vol. 16, no. 9, pp. 960–968, 2001.
- G. H. Kang, Y. H. Shim, H. Y. Jung, W. H. Kim, J. Y. Ro, and M. G. Rhyu, “CpG island methylation in premalignant stages of gastric carcinoma,” Cancer Research, vol. 61, no. 7, pp. 2847–2851, 2001.
- A. C. Ferrasi, N. A. Pinheiro, S. H. B. Rabenhorst et al., “Helicobacter pylori and EBV in gastric carcinomas: methylation status and microsatellite instability,” World Journal of Gastroenterology, vol. 16, no. 3, pp. 312–319, 2010.
- E. Yamamoto, M. Toyota, H. Suzuki et al., “LINE-1 hypomethylation is associated with increased CpG island methylation in Helicobacter pylori-related enlarged-fold gastritis,” Cancer Epidemiology Biomarkers and Prevention, vol. 17, no. 10, pp. 2555–2564, 2008.
- K. Chalitchagorn, S. Shuangshoti, N. Hourpai et al., “Distinctive pattern of LINE-1 methylation level in normal tissues and the association with carcinogenesis,” Oncogene, vol. 23, no. 54, pp. 8841–8846, 2004.
- S. Y. Park, E. J. Yoo, N. Y. Cho, N. Kim, and G. H. Kang, “Comparison of CpG island hypermethylation and repetitive DNA hypomethylation in premalignant stages of gastric cancer, stratified for Helicobacter pylori infection,” Journal of Pathology, vol. 219, no. 4, pp. 410–416, 2009.
- T. Hiyama, S. Tanaka, M. Yoshihara et al., “Chromosomal and microsatellite instability in sporadic gastric cancer,” Journal of Gastroenterology and Hepatology, vol. 19, no. 7, pp. 756–760, 2004.
- S. Yamaoka, H. Yamamoto, K. Nosho et al., “Genetic and epigenetic characteristics of gastric cancers with JC virus T-antigen,” World Journal of Gastroenterology, vol. 15, no. 44, pp. 5579–5585, 2009.
- Z. Xiong and P. W. Laird, “COBRA: a sensitive and quantitative DNA methylation assay,” Nucleic Acids Research, vol. 25, no. 12, pp. 2532–2534, 1997.
- A. S. Yang, M. R. Estécio, K. Doshi, Y. Kondo, E. H. Tajara, and J. P. Issa, “A simple method for estimating global DNA methylation using bisulfite PCR of repetitive DNA elements,” Nucleic Acids Research, vol. 32, no. 3, p. e38, 2004.
- E. Tahara, “Molecular mechanism of stomach carcinogenesis,” Journal of Cancer Research and Clinical Oncology, vol. 119, no. 5, pp. 265–272, 1993.
- L. A. Loeb, “Microsatellite instability: marker of a mutator phenotype in cancer,” Cancer Research, vol. 54, no. 19, pp. 5059–5063, 1994.
- L. Ottini, M. Falchetti, R. Lupi et al., “Patterns of genomic instability in gastric cancer: clinical implications and perspectives,” Annals of Oncology, vol. 17, supplement 7, pp. vii97–vii102, 2006.
- T. Sugai, W. Habano, Y. F. Jiao, M. Suzuki, A. Takagane, and S. I. Nakamura, “Analysis of genetic alterations associated with DNA diploidy, aneuploidy and multiploidy in gastric cancers,” Oncology, vol. 68, no. 4–6, pp. 548–557, 2005.
- C. Lengauer, K. W. Kinzler, and B. Vogelstein, “Genetic instability in colorectal cancers,” Nature, vol. 386, no. 6625, pp. 623–627, 1997.
- E. Tahara, “Genetic pathways of two types of gastric cancer,” IARC Scientific Publications, no. 157, pp. 327–349, 2004.
- T. Ohara, J. Kasanuki, H. Ohara et al., “Analysis of the differences in structural chromosomal aberrations of the gastric mucosa between H. pylori positive and negative gastric cancer patients: involvement of H. pylori in the onset of gastric cancer and examination of the mechanism in gastric carcinogenesis following H. pylori eradication,” Oncology Reports, vol. 16, no. 6, pp. 1333–1342, 2006.
- J. Jiricny, “The multifaceted mismatch-repair system,” Nature Reviews Molecular Cell Biology, vol. 7, no. 5, pp. 335–346, 2006.
- J. J. Kim, H. Tao, E. Carloni, W. K. Leung, D. Y. Graham, and A. R. Sepulveda, “Helicobacter pylori impairs DNA mismatch repair in gastric epithelial cells,” Gastroenterology, vol. 123, no. 2, pp. 542–553, 2002.
- H. Kim, J. Y. An, S. H. Noh, S. K. Shin, Y. C. Lee, and H. Kim, “High microsatellite instability predicts good prognosis in intestinal-type gastric cancers,” Journal of Gastroenterology and Hepatology, vol. 26, no. 3, pp. 585–592, 2011.
- C. R. Boland, S. N. Thibodeau, S. R. Hamilton et al., “A National Cancer Institute workshop on microsatellite instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer,” Cancer Research, vol. 58, no. 22, pp. 5248–5257, 1998.
- T. Watanabe, T. Kobunai, E. Toda et al., “Distal colorectal cancers with microsatellite instability (MSI) display distinct gene expression profiles that are different from proximal MSI cancers,” Cancer Research, vol. 66, no. 20, pp. 9804–9808, 2006.
- R. M. Xicola, X. Llor, E. Pons et al., “Performance of different microsatellite marker panels for detection of mismatch repair-deficient colorectal tumors,” Journal of the National Cancer Institute, vol. 99, no. 3, pp. 244–252, 2007.
- G. Y. Lauwers and R. H. Riddell, “Gastric epithelial dysplasia,” Gut, vol. 45, no. 5, pp. 784–790, 1999.
- H. Takenawa, M. Kurosaki, N. Enomoto et al., “Differential gene-expression profiles associated with gastric adenoma,” British Journal of Cancer, vol. 90, no. 1, pp. 216–223, 2004.
- S. Y. Park, S. W. Jeon, M. K. Jung et al., “Long-term follow-up study of gastric intraepithelial neoplasias: progression from low-grade dysplasia to invasive carcinoma,” European Journal of Gastroenterology and Hepatology, vol. 20, no. 10, pp. 966–970, 2008.
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