Single nucleotide polymorphisms of the APC gene and colorectal cancer risk: a case-control study in Taiwan
BMC Cancer volume 6, Article number: 83 (2006)
Colorectal cancer (CRC), which has become especially prevalent in developed countries, is currently the third highest cause of cancer mortality in Taiwan. Mutation of the adenomatous polyposis coli (APC) gene, a tumour suppressor, is thought to be an early event in colorectal tumourigenesis. To date, however, no large-scale screening for APC gene variants in Chinese subjects has been performed. The present study was undertaken to identify APC gene variants that are significantly associated with the occurrence of CRC in Taiwanese subjects.
In order to compare the genotype distribution of variant sites, the full-length APC genes of 74 healthy individuals and 80 CRC patients were sequenced.
Among the 154 Taiwanese subjects examined in this study, three new mutations, but no previously reported mutations, were found. One deletion at codon 460 leading to a frameshift and two missense mutations resulting in p.V1125A and p.S1126R substitutions were identified. Additionally, three high risk genotypes associated with three single nucleotide polymorphisms and one low risk genotype at codon 1822 were identified.
The findings of this case-control study are consistent with the proposal that Taiwanese subjects differ from other subjects with respect to phenotypic presentation of APC and CRC risk.
Colorectal cancer (CRC) has increased in incidence over the past two to three decades and has become especially prevalent in developed countries. For example, CRC is currently the second most common form of cancer and the third leading cause of cancer mortality in the United States . In Taiwan, CRC has become the fourth most common form of cancer and the third leading cause of death due to cancer. Approximately 10% of CRCs are attributable to genetic alterations whereas 90% occur sporadically .
Familial adenomatous polyposis (FAP), a disease inherited as an autosomal dominant, is characterized by the development of multiple colorectal polyps and possesses the potential to progress to CRC. FAP is now recognized to be caused by a functional mutation in the adenomatous polyposis coli (APC) gene [3, 4]. The APC gene is located at 5q21-q22, contains 15 exons, has a corresponding mRNA of approximately 10 kb, and encodes a large protein with multiple functional domains. The gene product has been linked with several important processes including cell adhesion, maintenance of cytoskeletal integrity and chromosomal stability, and regulation of the cell cycle . Previous findings are consistent with the proposals that the APC gene functions as a tumour suppressor and that somatic mutations in the APC gene predispose humans to development of FAP. The loss of APC function is currently thought to represent an event critical to colorectal tumourigenesis .
Although CRC attributable to mutations of the APC gene that lead to development of FAP represents less than 1% of all CRCs, APC germline mutations have close to 100% penetrance . Exon 15 of the APC gene encompasses 75% of the gene coding sequence and is the most common mutation site. Over 98% of mutations in this region are either nonsense or frameshift mutations. The codons 1061 and 1309 are the most common germline mutation sites, and mutations at either site often result in a frameshift [8, 9]. In addition, two missense germline mutations of APC are frequently reported. The first is the p.I1307K variant which is found in Ashkenazi Jews and is associated with a several-fold increased risk for development of multiple adenomas and CRC. The second is p.E1317Q, the mutation site of which lies between the first and second 20-amino acid β-catenin binding sites. This mutation has been proposed to suppress the APC/β-catenin pathway, thereby predisposing to the development of adenomas [10–12].
Somatic mutations in the APC gene are found in over 85% of sporadic colorectal adenomas and carcinomas . More than 60% of all such mutations are found within the sequence between codons 1286 and 1513 and termed the mutation cluster region (MCR) . Two hotspots for somatic mutations are found at codons 1286 and 1450; mutations at these sites often result in stop codons [8, 9]. Mutations in regions of the MCR encoding the 20-amino acid β-catenin binding sites may result in functional defects in the APC protein .
To improve current understanding of the genetics and biological functions of APC, additional screening of the gene for single nucleotide polymorphisms (SNPs) or missense mutations is needed. Furthermore, recognition of such mutations is essential in determining the inherited risks for CRC. APC gene variants may present as population-specific. To date, however, no large-scale screening for APC gene variants in Chinese subjects has been conducted. The present case-control study was performed to characterize SNP mutations of the APC gene in the Taiwanese population and to identify the variants that are significantly associated with the occurrence of CRC.
Health examinations were performed for 74 individuals at the Hualien Tzu Chi Medical Center and for 80 colorectal cancer patients at the Tri-Service General Hospital. All subjects were screened for colorectal tumors by colonscopy and none of them has the family history of CRC. Written informed consent was obtained from all subjects, and the study protocol was approved by The Protection of Human Subjects Institutional Review Board Tzu-Chi University and Hospital, IRB093-54.
The study group was comprised of 80 colorectal cancer patients and 74 healthy adults. The patient group consisted of 40 (50%) males of 63.6 ± 12.5 years of age (mean ± SD; range, 35–95 years) and 40 (50%) females of 59.2 ± 11.0 years of age (mean ± SD; range, 37–80 years). The mean age ± SD for all patients was 61.5 ± 12.0 years (range, 35–95 years). The health examination group consisted of 34 (45.3%) males of 55.8 ± 11.5 years of age (mean ± SD; range, 32–84 years) and 41 (54.7%) females of 53.0 ± 8.7 years of age (mean ± SD; range, 39–72 years). The mean age ± SD for all healthy adults was 54.3 ± 10.1 years (range, 32–84 years). In the patient group, there were 16 (20%) subjects with proximal tumors, 26 (32.5%) subjects with distal tumors, 38 (47.5%) subjects with rectal tumors, and there were 8 (10%) subjects with colorectal tumors in Duke's stage A, 24 (30%) in Duke's stage B, 38 (47.5%) in Duke's stage C and 10 (12.5%) in Duke's stage D.
Genomic DNA was extracted from 10 ml of whole blood through use of the Puregene Genomic DNA Purification Kit (Gentra Systems, Inc., Minneapolis, MN, USA). The extracted DNA was quantified with a DU 640 spectrophotometer (Beckman Instruments, Inc., Fullerton, CA, USA).
Gene amplification and DHPLC
The coding region of the APC gene was divided into 28 segments, each of which was amplified separately using the polymerase chain reaction (PCR). The primer pairs used in this study were designed for both PCR and denaturing high performance liquid chromatography (DHPLC; Transgenomic, Inc., Omaha, NE, USA) as previously described . All samples were amplified in 50-μl of a reaction mixture containing 50 ng genomic DNA, 10 mM Tris-HCl, 50 mM KCl, 2.5 mM MgCl2, 0.2 mM of each dNTP, 200 mM of each primer, and 0.15 U AmpliTaq Gold DNA polymerase (Applied Biosystems; Roche Molecular Systems, Inc., Branchburg, NJ, USA). The thermal cycling profile was composed of an initial denaturation step at 95°C for 10 min, 35 cycles of 30 sec of denaturation at 95°C, 30 sec of annealing at 55°C, and 1 min of extension at 72°C, with a final 10-min extension step at 72°C. DNA samples amplified from the same regions of APC genes were subjected to DHPLC and compared. When observed peaks differed in sharpness or appeared with more than 0.08 sec of difference from the main peak, potentially different DNA sequences were suspected. Such samples were therefore subjected to sequencing.
Sequencing reactions were performed with the BigDye Terminator v3.1 Cycle Sequencing Kit (Applied Biosystems, Foster City, CA, USA). Each sequencing reaction was amplified in a 10-μl reaction mixture containing 10–30 ng amplified DNA. The thermal cycling profile consisted of an initial denaturation step at 95°C for 10 sec, 25 cycles of 10 sec of denaturation at 95°C, 5 sec of annealing at 50°C, and 1 min of extension at 60°C. Primers used for direct sequencing reactions were identical to those used in the amplification reactions. Nucleotide sequences of both strands were determined with an ABI Prism 3100 Genetic Analyzer (Applied Biosystems, Foster City, CA, USA) equipped with a long-read sequencing capillary and a POP-4 sequencing polymer.
The sequence data collected from the ABI 3100 Genetic Analyzer were analyzed by software programs from Applied Biosystems. The analyzed sequence data were aligned through the use of BioEdit 7.0.5 software . The Chi-square tests for Hardy-Weinberg equilibrium, the Chi-square and Fisher's exact tests for differences between the patient and health examination groups, and logistic regression analyses for odds ratios (without adjusting for other variables) were processed by SAS 9.1.
When the coding regions of APC genes of all 154 subjects enrolled in the study were sequenced, 12 SNPs and 1 deletion mutation were identified (Table 1). Of these variants, 8 SNPs were located within exon 15, 2 SNPs within exon 11, 1 SNP within exon 9, 1 SNP within exon 13, and 1 deletion within exon 10. Of the 12 SNPs, 9 are silent substitutions and 3 are responsible for the amino acid changes p.V1125A, p.S1126R and p.D1822V. Ten SNPs were identified in the health examination group and 2 of these SNPs, g.1488A>T and g.3378C>G, were not found in the patient group. Ten SNPs and 1 deletion mutation were found in the patient group and 3 of these variants, g.1050T>G, g.1378delG and g.4725A>G, were not found in the health examination group (Table 1).
The single base pair deletion, g.1378delG, which is located in exon 10, was found only in one individual in the patient group. This subject presented with a heterozygous genotype, confirmed by repeated forward and reverse sequencing. Prevalence of this mutation, which is reported here for the first time, was not significantly different between the patient and health examination groups.
Of the 3 observed missense substitutions, p.V1125A and p.S1126R represent variants not previously reported. p.V1125A was identified in three subjects in the patient group and in one subject in the health examination group, but p.S1126R was found only in the health examination group. However, the prevalence of these variants did not differ significantly between the patient and health examination groups. The characteristics of the subjects in the patient group with g.1378delG deletion or g.3374T>C (p.V1125A) are listed in Table 2. Prevalence of the p.D1822V variant, which has been observed previously [17–19], was significantly different between the patient and health examination groups. When this variant was analyzed further by determination of the odds ratio, a low risk for CRC was observed for subjects displaying the AT genotype (Table 3).
Of the 12 SNPs identified, only g.1458T>C and observed within the patient group displayed significant deviation from Hardy-Weinberg equilibrium (p = 0.002). To ascertain whether differences in the genotype distribution existed between the health examination group and patient group at these SNP sites, the Chi-square test and the Fisher's Exact test were performed. Significant differences were observed at g.1458T>C (p = 0.0012), g.4479G>A, (p = 0.0057), g.5268T>G (p = 0.0023). Analysis of the odds ratio for each genotype at these three sites revealed that g.1458T>C and g.4479G>A were significant and g.5268T>G was close to significant associated with a higher risk genotype (Table 3).
In this case-control study involving the screening of 74 healthy Taiwanese adults and 80 Taiwanese CRC patients for germline variants throughout the entire coding region of the APC gene, three new mutations were identified. No mutations reported in previous studies, including those at codons 1061 and 1309 which are considered the most common mutation sites, were identified. The absence in these Taiwanese subjects of the Caucasian-specific mutations p.E1317Q and p.I1307K that are known to cause missense changes is in accord with the findings of Guo et al. . Additionally, Asian-specific variants such as the odd mutations reported in a Japanese study  were not displayed by any of the Taiwanese subjects in the present study. These observations are consistent with the proposals that the different presentations of the APC gene in these Taiwanese subjects are due to population differences and that the new mutations found in this study represent Taiwanese-specific hotspot mutations.
The three new mutations identified in the present study include a one base pair deletion and two missense substitutions. The one base pair deletion occurs at codon 460 of exon 10 and will cause a frameshift resulting in expression of a truncated protein. The two missense substitutions, p.V1125A and p.S1126R, occur in close proximity to the first 15-amino acid β-catenin binding repeat (amino acids 1136–1151) located at the center of the β-catenin down-regulation domain. Such substitutions may result in disruption of the putative cell signaling function of the APC protein; however, this needs to be demonstrated experimentally. It should be noted that all three mutations presented with low frequency in subject population of the present study and that the p.S1126R mutation was observed only in the health examination group. The sites at which these mutations occur, therefore, may not represent hotspots commonly associated with CRC. Nevertheless, the presence of these mutations may result in development of CRC. Long-term monitoring of persons who present with these mutations is therefore considered essential.
The frequency distribution of the 13 variants identified in the present study differed significantly between the health examination group and patient group at g.1458T>C, g.4479G>A, g.5268T>G and g.5465A>T (Table 1, p < 0.05 by the Chi-square test or Fisher's Exact test). Further analysis by logistic regression indicated that genotypes at g.1458T>C, g.4479G>A and g.5268T>G had high odds ratios for CRC (Table 3). These genotypes may therefore serve as markers predicting the development of CRC. The polymorphism p.D1822V, which was observed in the present study, is located in close proximity to the fifth APC cysteine-rich region β-catenin binding repeat (amino acids 1840–1866). p.D1822V is a missense variant previously shown to be a common polymorphism unrelated to the risk of developing CRC or colorectal adenoma [18, 19]. However, two previous studies of CRC demonstrated significant gene-environment interactions between the p.D1822V polymorphism and consumption of a low-fat diet and postmenopausal hormone use [19, 22]. Although no TT homozygotes for this site were identified in the present study, AT heterozygotes for this site were identified who had a low odds ratio for CRC (Table 3). The presence of a T allele at this site may therefore serve to protect against development of CRC.
Certain SNPs of APC genes were previously reported to be differentially distributed among different populations. Of the 10 SNPs identified in the present study the only SNP with a significantly different allele distribution, as determined by comparison with the East Asian population through use of the NCBI SNP databank (p <0.05, Chi-square test), was g.4479G>A. Further analysis revealed that an AA genotype for this SNP is associated with a higher risk for CRC. This observation implicates this genotype as a likely marker for CRC in the Taiwanese population. The other two SNPs, g.1458T>C and g.5268T>G, with higher risk genotypes for CRC were not found to have an allelic distribution different from other East Asian populations as determined through use of the NCBI SNP databank. These SNPs may therefore serve as markers for CRC specific to East Asian populations.
Investigations of the relationships existing between SNPs or germline mutations in the APC gene and occurrence of CRC should enable more accurate predictions of CRC. Furthermore, extensive screening of FAP patients should lead to a better understanding of the importance of events underlying development of CRC. Future studies of various high-risk APC gene mutations may also lead to improvements in therapy and, therefore, to increased survival of CRC patients.
Among the APC genes of the 154 Taiwanese subjects examined in this case-control study three new mutations, but no previously reported mutations, were identified. Taiwanese subjects therefore appear to differ from other subjects with respect to the genotypic presentation of APC. Three high risk genotypes at 3 SNPs and one low risk genotype at codon 1822 were identified in this study. The latter was reported previously to have no association with CRC.
polymerase chain reaction
single nucleotide polymorphism
denaturing high performance liquid chromatography
Jemal A, Murray T, Ward E, Samuels A, Tiwari RC, Ghafoor A, Feuer EJ, Thun MJ: Cancer statistics. CA Cancer J Clin. 2005, 55: 10-30.
Weitz J, Koch M, Debus J, Hohler T, Galle PR, Buchler MW: Colorectal cancer. Lancet. 2005, 365: 153-165. 10.1016/S0140-6736(05)17706-X.
Joslyn G, Carlson M, Thliveris A, Albertsen H, Gelbert L, Samowitz W, Groden J, Stevens J, Spirio L, Robertson M: Identification of deletion mutations and three new genes at the familial polyposis locus. Cell. 1991, 66: 601-613. 10.1016/0092-8674(81)90022-2.
Kinzler KW, Nilbert MC, Su LK, Vogelstein B, Bryan TM, Levy DB, Smith KJ, Preisinger AC, Hedge P, McKechnie D: Identification of FAP locus genes from chromosome 5q21. Science. 1991, 253: 661-665.
Narayan S, Roy D: Role of APC and DNA mismatch repair genes in the development of colorectal cancers. Mol Cancer. 2003, 2: 41-10.1186/1476-4598-2-41.
Lamlum H, Papadopoulou A, Ilyas M, Rowan A, Gillet C, Hanby A, Talbot I, Bodmer W, Tomlinson I: APC mutations are sufficient for the growth of early colorectal adenomas. Proc Natl Acad Sci U S A. 2000, 97: 2225-2228. 10.1073/pnas.040564697.
Bisgaard ML, Fenger K, Bulow S, Niebuhr E, Mohr J: Familial adenomatous polyposis (FAP): frequency, penetrance, and mutation rate. Hum Mutat. 1994, 3: 121-125. 10.1002/humu.1380030206.
Fearnhead NS, Britton MP, Bodmer WF: The ABC of APC. Hum Mol Genet. 2001, 10: 721-733. 10.1093/hmg/10.7.721.
Laurent-Puig P, Beroud C, Soussi T: APC gene: database of germline and somatic mutations in human tumors and cell lines. Nucleic Acids Res. 1998, 26: 269-270. 10.1093/nar/26.1.269.
Frayling IM, Beck NE, Ilyas M, Dove-Edwin I, Goodman P, Pack K, Bell JA, Williams CB, Hodgson SV, Thomas HJ, Talbot IC, Bodmer WF, Tomlinson IP: The APC variants I1307K and E1317Q are associated with colorectal tumors, but not always with a family history. Proc Natl Acad Sci U S A. 1998, 95: 10722-10727. 10.1073/pnas.95.18.10722.
Lamlum H, Al Tassan N, Jaeger E, Frayling I, Sieber O, Reza FB, Eckert M, Rowan A, Barclay E, Atkin W, Williams C, Gilbert J, Cheadle J, Bell J, Houlston R, Bodmer W, Sampson J, Tomlinson I: Germline APC variants in patients with multiple colorectal adenomas, with evidence for the particular importance of E1317Q. Hum Mol Genet. 2000, 9: 2215-2221.
Groves C, Lamlum H, Crabtree M, Williamson J, Taylor C, Bass S, Cuthbert-Heavens D, Hodgson S, Phillips R, Tomlinson I: Mutation cluster region, association between germline and somatic mutations and genotype-phenotype correlation in upper gastrointestinal familial adenomatous polyposis. Am J Pathol. 2002, 160: 2055-2061.
Kinzler KW, Vogelstein B: Lessons from hereditary colorectal cancer. Cell. 1996, 87: 159-170. 10.1016/S0092-8674(00)81333-1.
Miyoshi Y, Nagase H, Ando H, Horii A, Ichii S, Nakatsuru S, Aoki T, Miki Y, Mori T, Nakamura Y: Somatic mutations of the APC gene in colorectal tumors: mutation cluster region in the APC gene. Hum Mol Genet. 1992, 1: 229-233.
Wei SC, Su YN, Tsai-Wu JJ, Wu CH, Huang YL, Sheu JC, Wang CY, Wong JM: Genetic analysis of the APC gene in Taiwanese familial adenomatous polyposis. J Biomed Sci. 2004, 11: 260-265.
Hall T: Ibis Therapeutics Carlsbad CA. 9200
Wallis YL, Morton DG, McKeown CM, Macdonald F: Molecular analysis of the APC gene in 205 families: extended genotype-phenotype correlations in FAP and evidence for the role of APC amino acid changes in colorectal cancer predisposition. J Med Genet. 1999, 36: 14-20.
Ruiz-Ponte C, Vega A, Conde R, Barros F, Carracedo A: The Asp1822Val variant of the APC gene is a common polymorphism without clinical implications. J Med Genet. 2001, 38: E33-10.1136/jmg.38.10.e33.
Tranah GJ, Giovannucci E, Ma J, Fuchs C, Hunter DJ: APC Asp1822Val and Gly2502Ser polymorphisms and risk of colorectal cancer and adenoma. Cancer Epidemiol Biomarkers Prev. 2005, 14: 863-870. 10.1158/1055-9965.EPI-04-0687.
Guo J, Lim R, Soo R, Leong A, Lee SC: APC I1307K and the E1317Q variants are not present in Chinese colorectal cancer patients. Genet Med. 2004, 6: 237-238.
Nishisho I, Nakamura Y, Miyoshi Y, Miki Y, Ando H, Horii A, Koyama K, Utsunomiya J, Baba S, Hedge P: Mutations of chromosome 5q21 genes in FAP and colorectal cancer patients. Science. 1991, 253: 665-669.
Slattery ML, Samowitz W, Ballard L, Schaffer D, Leppert M, Potter JD: A molecular variant of the APC gene at codon 1822: its association with diet, lifestyle, and risk of colon cancer. Cancer Res. 2001, 61: 1000-1004.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/6/83/prepub
This study was supported by grants from the National Science Council NSC94-2320-B-303-001, Taipei, Taiwan.
The author(s) declare that they have no competing interests.
SPC carried out the acquisition of data, data analysis, drafted and wrote the manuscript. STT, YLH, YLC, YCC and CCW participated in the acquisition of data, sequence and wrote the manuscript. SZL, HJH, SWJ conceived of the study, and participated in its design and coordination and helped to draft the manuscript. All authors read and approved the final manuscript.
About this article
Cite this article
Chen, SP., Tsai, ST., Jao, SW. et al. Single nucleotide polymorphisms of the APC gene and colorectal cancer risk: a case-control study in Taiwan. BMC Cancer 6, 83 (2006). https://doi.org/10.1186/1471-2407-6-83
- Familial Adenomatous Polyposis
- Adenomatous Polyposis Coli
- Familial Adenomatous Polyposis Patient
- Adenomatous Polyposis Coli Gene
- East Asian Population