- Open Access
Absence of germline mono-allelic promoter hypermethylation of the CDH1 gene in gastric cancer patients
© Yamada et al; licensee BioMed Central Ltd. 2009
- Received: 12 March 2009
- Accepted: 12 August 2009
- Published: 12 August 2009
Germline mono-allelic promoter hypermethylation of the MLH1 or MSH2 gene in families with hereditary nonpolyposis colorectal cancer has recently been reported. The purpose of this study was to evaluate if germline promoter hypermethylation of the tumor suppressor gene CDH1 (E-cadherin) might cause predisposition to gastric cancer.
We prepared two groups of samples, a group of blood samples from 22 patients with familial gastric cancer or early-onset gastric cancer selected from among 39 patients, and a group of non-cancerous gastric tissue samples from 18 patients with sporadic gastric cancer showing loss of CDH1 expression selected from among 159 patients. We then investigated the allele-specific methylation status of the CDH1 promoter by bisulfite sequencing of multiple clones.
Although there was a difference between the methylation level of the two alleles in some samples, there was no mono-allelic promoter hypermethylation in any of the samples.
These results suggest that germline mono-allelic hypermethylation of the CDH1 promoter is not a major predisposing factor for gastric cancer.
- Gastric Cancer
- Gastric Cancer Patient
- CDH1 Gene
- Hereditary Diffuse Gastric Cancer
- CDH1 Expression
Gastric cancer is one of the most common cancers worldwide, including in Japan, and gastric carcinogenesis is a multistep process in which environmental and genetic factors interact [1–6]. Among the genetic factors, the CDH1 gene, alternatively referred to as the E-cadherin gene, is one of the most important tumor suppressor genes in gastric cancer , and mutations, chromosomal deletions, and epigenetic modifications have been reported as mechanisms that cause CDH1 inactivation [6–17]. Somatic CDH1 mutations have been found in about 50% of diffuse-type gastric cancers , and germline CDH1 mutations have been reported in familial gastric cancers in several ethnic groups [6, 8–13]. Promoter region hypermethylation, histone deacetylation, and chromatin condensation have been reported as epigenetic events in the CDH1 gene [14–17]. Among these mechanisms that cause CDH1 inactivation, inactivating germline mutations are the only genetic mechanism which is inherited in gastric cancer. Furthermore, since the germline CDH1 mutations have been found in only a certain percentage of familial gastric cancers, it is reasonable to hypothesize that CDH1 inactivation due to a previously unknown mechanism or inactivation of another gene plays a role in predisposing to gastric cancer. Interestingly, a germline mono-allelic hypermethylation of the MLH1 or MSH2 promoter has recently been reported in a subset of families with hereditary nonpolyposis colorectal cancer (HNPCC) [18–21]. Although mutations or chromosomal deletions in MLH1 and MSH2 have long been known to be hereditary genetic factors in HNPCC patients , such a germline epigenetic modification is a novel mechanism for the disease. Based on all of the above, we hypothesized that germline mono-allelic hypermethylation of the CDH1 promoter is responsible for gastric cancer, and in the present study we tested this hypothesis by examining the lesions of 39 patients with familial gastric cancer or early-onset gastric cancer. Furthermore, since germline CDH1 mutations are rarely found in gastric cancer patients with no family history of gastric cancer [23, 24], we considered it worth examining patients with sporadic gastric cancer, even though the possibility of detecting germline mono-allelic hypermethylation of the CDH1 promoter may be small in that group.
Tissue samples, cell lines, and nucleic acid extraction
Although the diagnostic criteria for hereditary diffuse gastric cancer have been defined by the International Gastric Cancer Linkage Consortium , the Consortium also noted that the criteria should not be applied in Japan and Korea, where the background incidence of gastric cancer is high. In the present study we tentatively used the criterion "a proband and one or more cases of gastric cancer in the first-degree relatives" and called the cases collected familial gastric cancer. In this study "early-onset gastric cancer" is defined as gastric cancer diagnosed before 50 years of age. Blood samples were collected from 39 patients with familial gastric cancer or early-onset gastric cancer [12, 25], and all of whom had been shown to be negative for germline CDH1 mutations [12, 25]. Non-cancerous gastric tissue was collected from 159 gastric cancer patients treated at the Hamamatsu University Hospital. HeLa, HL-60, H358, and HT-29 cell lines were purchased from the American Type Culture Collection (Manassas, VA), and Lu-135 and MKN74 cell lines were purchased from Human Science Research Resource Bank (Osaka, Japan). Genomic DNA was extracted with a QIAamp DNA Blood Maxi Kit (QIAGEN, Valencia, CA) or with a DNeasy Tissue Kit (QIAGEN). Total RNA was extracted with an RNeasy Mini Kit (QIAGEN). The research protocol was approved by the Institutional Review Board of Hamamatsu University School of Medicine.
Reverse transcription (RT)-polymerase chain reaction (PCR) analysis
Total RNA was converted to cDNA by using the SuperScript First-Strand Synthesis System for RT-PCR (Invitrogen, Carlsbad, CA) according to the manufacturer's instructions. PCR amplification was performed using the following sets of primers: 5'-AGA ACG CAT TGC CAC ATA CAC-3' and 5'-GAG GAT GGT GTA AGC GAT GG-3' for the CDH1 transcripts and 5'-CCA AGG TCA TCC ATG ACA AC-3' and 5'-CAC CCT GTT GCT GTA GCC A-3' for the GAPDH transcripts. PCR products were fractionated by electrophoresis on a 2.0% agarose gel and stained with ethidium bromide, and the gel was examined under UV light. A 100-bp DNA ladder (New England Biolabs, Beverly, MA) was used.
The -348_-347insA, -161C>A, and -73A>C polymorphisms in the CDH1 promoter region were genotyped by PCR-restriction fragment length polymorphism (RFLP) analysis. These polymorphisms are denoted based on the GenBank accession number NT_010498 (CDH1 reference sequence used in this study). The -161C>A polymorphism has also been reported as the -160C>A polymorphism in several previous papers . The CDH1 promoter region was amplified by PCR with HotStarTaq DNA polymerase (QIAGEN) and the following set of primers: 5'-GCT ACT AGA GAG GCT GGG GC-3' and 5'-TCA CAG GTG CTT TGC AGT TC-3'. The PCR products were digested with Bsm AI for the -348_-347insA polymorphism and with Bst EII for the -161C>A and -73A>C polymorphisms. The digestion products were separated by electrophoresis on a 2.0% agarose gel and stained with ethidium bromide, and the gel was examined under UV light. To validate the results of the PCR-RFLP analysis, some PCR products exhibiting a different genotype in the PCR-RFLP analysis were randomly selected and directly sequenced with a BigDye Terminator Cycle Sequencing Reaction Kit (Applied Biosystems, Tokyo, Japan) and an ABI 3100 Genetic Analyzer (Applied Biosystems). Deviation of genotype distribution from the Hardy-Weinberg equilibrium (HWE) was tested with SNPAlyze software (Dynacom, Yokohama, Japan).
Paraffin-embedded tissue sections were deparaffinized, rehydrated, and antigen-retrieved. The sections were then treated with 3% hydrogen peroxide to block endogenous peroxidase activity. Next, the sections were incubated with an anti-CDH1 monoclonal antibody (clone 36B5; Novocastra, Newcastle, UK), and then with dextran polymer conjugated with goat anti-mouse IgG and horseradish peroxidase (ChemMate Envision Kit, DAKO, Kyoto, Japan). The antigen-antibody complex was visualized with 3,3'-diaminobenzidine tetrahydrochloride and counterstained with hematoxylin. This analysis was performed with a DAKO autostainer (DAKO) . Hematoxylin-eosin (H-E) stained slides were also prepared.
Allele-specific methylation analysis
A 500 ng sample of genomic DNA was treated with sodium bisulfite using the EpiTect Bisulfite Kit (QIAGEN) according to the manufacturer's instructions. The CDH1 promoter region was amplified by PCR with HotStarTaq DNA polymerase (QIAGEN) and the bisulfite-treated DNA. The primers used were 5'-TTT TTT TTG ATT TTA GGT TTT AGT GAG-3' and 5'-ACT CCA AAA ACC CAT AAC TAA CC-3' for DNA extracted from the cell lines and 5'-TGG TGG TGT GTA TTT GTA TTT TTA GGA G-3' and 5'-ACT CCA AAA ACC CAT AAC TAA CC-3' for DNA extracted from blood or gastric tissue. The PCR conditions consisted of initial denaturation at 95°C for 15 min, 45 cycles of denaturation at 94°C for 30 sec, annealing at 59°C for 30 sec, and extension at 72°C for 1 min, and then a final extension at 72°C for 10 min. The PCR product was subcloned into a pGEM-T Easy vector (Promega, Madison, WI). At least 8 clones were sequenced with a BigDye Terminator Cycle Sequencing Reaction Kit (Applied Biosystems) and an ABI 3100 Genetic Analyzer (Applied Biosystems). The sequencing results and genotyping results for the -348_-347insA, -161C>A, or -73A>C polymorphisms described in "Genotyping analysis" section were used to evaluate allele-specific methylation status in the analysis of blood and gastric tissue.
Inverse association between CDH1 promoter methylation level and CDH1 mRNA expression level in human cell lines
Absence of germline mono-allelic hypermethylation in the CDH1 promoter in gastric cancer
Distribution of the genotypes of the three CDH1 promoter polymorphisms in gastric cancer patients
Number of patients with a heterozygous genotype (%)
Number of patients homozygous for a varinat allele (%)
Variant allele frequency
In this study blood from 22 patients with familial gastric cancer or early-onset gastric cancer and non-cancerous gastric tissues from 18 patients with sporadic gastric cancer showing loss of CDH1 expression was analyzed for allele-specific methylation status of the CDH1 promoter by bisulfite sequencing analysis. Although a difference between the methylation level of the two CDH1 alleles was found in some non-cancerous gastric tissue samples, no mono-allelic promoter hypermethylation of the CDH1 gene was detected in any of them. This finding suggests that germline promoter hypermethylation of the CDH1 gene is not involved in any mechanism that causes susceptibility to gastric cancer. This is the first report of an investigation into whether germline mono-allelic hypermethylation of the CDH1 promoter is a predisposing factor for gastric cancer.
Since bisulfite allelic sequencing enables detailed, base-by-base measurement of CpG methylation and discrimination between the wild-type and variant type at the polymorphism site, we used it to determine methylation status in the CDH1 promoter region. The results showed that CDH1 promoter methylation status determined by the bisulfite sequencing analysis was inversely associated with mRNA expression status of the CDH1 gene in the human cell lines, indicating that a valid system had been established. However, no mono-allelic hypermethylation of the CDH1 promoter was found in any of the samples, suggesting that it is not a predisposing factor for gastric cancer. Caution is required, however, since the absence of germline mono-allelic promoter hypermethylation in this study may have been due to the limited number of patients analyzed and Hitchins et al. reported a very low incidence of germline mono-allelic hypermethylation of the MLH1 promoter in HNPCC (1 out of 160 HNPCC candidates) , it is impossible to rule out the possibility that analysis of a larger number of gastric cancer patients would reveal cases with germline mono-allelic hypermethylation of the CDH1 promoter. However, there were two reasons for the limited number of patients utilized for the allele-specific methylation analysis in our study. One reason is that the incidence of familial gastric cancer or early-onset gastric cancer is relatively low, and the other is that selection in regard to CDH1 promoter polymorphisms and CDH1 expression was necessary in this study. We therefore think that the results of our investigation of these selected samples are very important. Since all of the patients with familial gastric cancer or early-onset gastric cancer whose samples we analyzed had already been shown to be negative for germline CDH1 mutation [12, 25], genetic or epigenetic events in other genes may have been involved in the gastric carcinogenesis in those patients.
Although no mono-allelic hypermethylation of the CDH1 promoter was detected in this study, various levels of methylation of CpG sites in the CDH1 promoter were detected in all of the samples. This finding is compatible with findings reported previously [30, 31] and may be related to aging or Helicobacter pylori infection as reported in those papers [30, 31]. Interestingly, there were differences between the two alleles in methylation level of the CDH1 promoter in some non-cancerous gastric tissue samples. Allele-specific methylation of the CDH1 promoter has been reported to be the second genetic hit in gastric cancer tissue from patients with familial gastric cancer , but the mechanism underlying the CDH1 allele-specific methylation has not been elucidated in either non-cancerous or cancerous gastric tissue. Future investigation of this point should improve our understanding of gastric carcinogenesis.
Since germline mono-allelic promoter hypermethylation and transgenerational inheritance of such an epigenetic event is a recent finding in humans, there have been only a small number of papers documenting the germline epigenetic modification. Heritable germline mono-allelic hypermethylation of the MLH1 or MSH2 gene has been found in a subset of families with HNPCC [18–21]. On the other hand, similar investigation of the APC gene in patients with familial adenomatous polyposis (FAP), attenuated FAP, and hyperplastic polyposis, of the BRCA1 gene in patients with familial breast cancer, and of the CDKN2A gene in patients with familial melanoma have revealed no germline mono-allelic promoter hypermethylation of any of these genes [32–34]. Based on these findings and the results of our own study, germline mono-allelic hypermethylation is unlikely to be present in all genes responsible for hereditary cancer syndromes. Thus, it will be important to identify genes with germline epigenetic modifications in the future, because the results will be useful in making a precise diagnosis and in conducting surveillance and management of cancer patients and their family members.
In this study the distribution of the genotypes of the three CDH1 promoter polymorphisms was in HWE, and the results of PCR-RFLP analysis were confirmed by direct sequencing in some samples. This means our genotyping was performed properly, and proper genotyping was important to selecting the gastric cancer patients in our study. Since there is a CDH1 haplotype associated with increased gastric cancer risk and the haplotype contains the -161A allele , the genotyping method will be also valuable for evaluating the risk of gastric cancer.
There are two main histopathological types of gastric cancer, a diffuse-type and an intestinal-type. The 5-year survival rate has been reported to be lower for diffuse-type gastric cancer than for intestinal-type gastric cancer, and the incidence of peritoneal recurrence has been reported to be higher in diffuse-type gastric cancer than in intestinal-type gastric cancer [35, 36]. Although no germline mono-allelic hypermethylation of the CDH1 promoter was found in this study, we believe it is important to continue to evaluate CDH1 gene status from various standpoints, because CDH1 inactivation is closely related to the pathogenesis of diffuse-type gastric cancer.
The present results suggest that germline mono-allelic hypermethylation of the CDH1 promoter is not a major predisposing factor for gastric cancer.
We acknowledge Mr. T. Kamo (Hamamatsu Univ Sch Med) for technical assistance. HY and MG are COE research assistants in Hamamatsu Univ Sch Med. This work was supported by grants from the Ministry of Health, Labour and Welfare (19–19), the Japan Society for the Promotion of Science (19790286), the Ministry of Education, Culture, Sports, Science and Technology (20014007), the 21st Century COE program, and the Smoking Research Foundation.
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