- Open Access
Genetic polymorphisms in XRCC1 genes and colorectal cancer susceptibility
- Yi Huang†1,
- Xiaohua Li†2,
- Jing He†3,
- Lin Chen3,
- Huaxing Huang4,
- Mengdi Liang3,
- Qiannan Zhu3,
- Yaoyu Huang3,
- Li Wang3,
- Chunji Pan2 and
- Tiansong Xia3Email author
© Huang et al. 2015
- Received: 23 February 2015
- Accepted: 14 July 2015
- Published: 15 August 2015
The objective of this study is to investigate the association among the polymorphisms of XRCC1 gene, smoking, drinking, family history of tumors, and the risk of colorectal cancer (CRC) in the population of Han nationality in Jiangsu Province, China.
A case–control study of 320 patients with CRC and 350 cancer-free subjects as a control group was conducted. The three polymorphic sites, codons 194, 280, and 399, of XRCC1 genes were analyzed by PCR-RFLP.
We find that heavy smoking (>500 cigarettes per year) significantly increased the susceptibility of CRC (OR = 1.89, 95 % confidence interval (CI) 1.27–2.84) after stratification by total smoking amount. There was also significant difference between cases and controls when family history of tumors (OR = 2.96, 95 % CI 1.76–4.99) was considered. Comparing with individuals carrying XRCC1 399Arg/Arg genotype, the subjects with 399Arg/Gln (OR = 1.46, 95 % CI 1.06–2.01) or 399Gln/Gln genotype (OR = 1.93, 95 % CI 1.05–3.54) had a significantly increased risk for CRC. Taking smoking and drinking habits into consideration, we found that subjects with heavy smoking history and XRCC1 194Arg allele had the significantly increased risk for CRC (OR = 2.91, 95 % CI 1.35–6.24). Individuals, who carry 399Gln allele and have a heavy smoking (OR = 2.72, 95 % CI 1.52–4.89) or drinking habit (OR = 1.98, 95 % CI 1.06–3.67), also have higher risk. In smoking population, 194Arg (P = 0.491) and 399Gln (P = 0.912) had not significantly increased risk for CRC, so did 399Gln (P = 0.812) in smoking population.
Individuals carrying XRCC1 399Gln allele with a smoking or drinking habit were in increased risk, and heavy-smoking subjects with 194Arg allele also have higher risk for CRC in the Han nationality population of Jiangsu Province, which also showed a positive correlation with exposure dose of tobacco. But XRCC1 399Gln allele or 194Arg allele were not independent risk factors for CRC in smoking or drinking population.
- Colorectal cancer
- Molecular epidemiology
In the Western countries, colorectal cancer (CRC) is the second most common cancer-related cause of death . According to a report of World Health Organization, an estimated 147,500 new cases of colorectal cancer are diagnosed in the world per year, whereas in China, more and more new cases of CRC are diagnosed every year, and now, the risk of CRC is 13.29/100,000 in the Han nationality population of China .
Difference in DNA repair capacity (DRC) has been considered to exert an influence on tumor susceptibility , and reduced DRC might result in a higher risk for many people in developing cancer . The mechanism of CRC development is similar to other majority tumors, which is dependent on the interactions of genetic factors and environmental agents . Nowadays, the research on the relationship between genotypic polymorphism of DNA repair enzymes and tumor susceptibility has become a focus because living organisms suffer continuous damage from diverse environmental agents and normal cellular metabolism products and DNA repair is essential in protecting the genome of cells from environmental hazards, such as tobacco smoking and alcohol drinking.
Smoking is a rich source of reactive oxygen species and chemical carcinogens, and many studies have proved the close relation between smoking and the development of all kinds of tumors. Reactive oxygen species, coming from burning tobacco, can cause direct damage to DNA by initiating lipid peroxidation and oxidizing proteins. Moreover, chemical carcinogens in cigarette smoke (i.e., polycyclic aromatic hydrocarbons, nitrosamines, and arylamines) can induce bulky adducts in crypt cells, thus also contributing to the formation of mutations in the colon . In addition, alcohol can act as a cocarcinogen by facilitating the absorption of carcinogens, and as a carcinogen due to its conversion to acetaldehyde in the colon lumen, which can form DNA adducts, such as N2-ethyl-2-deoxyguanosine and 1,N2-propanodeoxyguanosine , and induce oxidative DNA damage, such as DNA strand breaks .
Although XRCC1 has no known enzymatic activity, it can interact with several important repair proteins through its different domains, such as DNA ligase III, DNA polymerase β, poly(ADP-ribose) polymerase (PARP) 1 and 2, human AP endonuclease, polynucleotide kinase (PNK), human 8-oxoguanine DNA glycosylase (OGG1), proliferating cell nuclear antigen (PCNA), etc. . A complex system of DNA repair enzymes has a vital role in protecting the genome of cells from all kinds of carcinogenic exposure. The DNA repair enzyme XRCC1 is thought to be involved in base excision repair (BER) of oxidative DNA and single-strand break (SSB) repair .
At present, three common polymorphisms of codon 194, codon 280, and codon 399 , which lead to amino acid substitutions in XRCC1 gene, have been found in the population of Han nationality in China. But, studies focused on the relation between these polymorphic sites, and CRC susceptibility in Han Chinese was few. More importantly, foreign population studies about XRCC1 polymorphisms related with CRC were inconsistent. Therefore, this study was performed in the Han people of Jiangsu Province in order to reveal the associations among the genetic polymorphisms of XRCC1 genes, smoking or drinking habit, family history of tumors, and CRC susceptibility.
Between April 2004 and October 2008, a total of 320 CRC patients, who had been diagnosed with CRC through biopsy of fibrocolonoscope or operation, and 350 age- and gender-matched control patients with other nontumorous diseases were included in this study after giving informed consent. The mean age in cases was 64.2 versus 65.3 years in controls. All subjects were ethnic Han Chinese, were able to answer relative questions clearly, and were permanently residing in Jiangsu Province, China. Serological (carcino-embryonic antigen, CEA), physical, and fibrocolonoscope examinations were conducted on all controls to exclude the possibility of CRC, and any control would be excluded from this study if he had any previous cancer diagnosis.
By using a uniform questionnaire, a face-to-face interview, and a review of medical records, we collected some information for every subject, including general characteristics, personal medical history, family cancer history, and history of smoking and alcohol drinking.
Drinking habit was defined as drinking at least three times per week lasting more than 5 years [6, 7]. Family history of tumors was defined as any cancer in first-degree relatives (parents, siblings, or children). In our research, smoking more than five cigarettes per day for more than 5 years was defined as a smoking habit. The unit cigarette × year for evaluating accumulative smoking amount was defined as one cigarette per day for 1 year. Slight smoking was defined when the accumulative smoking amount was no more than (≤) 500 cigarettes per year (the integer of average), and heavy smoking was defined when the accumulative smoking amount was more than (>) 500 cigarettes per year [11, 12].
Collection for blood specimens
With consent from patients, 5 mL of peripheral vein blood was collected. After anticoagulated with EDTA, the specimens were immediately stored at −70 °C for genotyping.
Extraction of genome DNA
Genomic DNA was isolated and purified from anticoagulated blood (5 mL) by the traditional phenol/chloroform extraction and ethanol precipitation, dissolved in TE buffer (pH = 7.4), and stored at −20 °C.
Analysis of genotypes
Primers were synthesized by Bioasia Co. (Shanghai, China), and 10 polymerase chain reaction (PCR) reaction buffers, 25 mmol/L MgCl2, 10 mmol/L dNTP, Taq DNA polymerase, and four kinds of restriction endonucleases (Pvu II, Rsa I, and Msp I) were all purchased from New England Biolabs (Ipswich, MA, USA).
Epidata 3.0 software (EpiData Association, Odense, Denmark) was used to input the data, and SPSS 12.0 software (SPSS, Chicago, IL, USA) was used for statistical analysis. T test was used to evaluate mean difference between cases and controls, Hardy–Weinberg test for assessing heredity equilibrium, and χ 2 test for enumeration data and the analysis of their reciprocity. The risk of CRC was evaluated with odds ratio (OR) and 95 % confidence interval (CI).
Investigators were trained uniformly, and in-person interviews were conducted in a hospital. Results of investigation or experiment of 5 % samples were checked randomly. Biolong Gene Limited Company sequenced the PCR amplified products. Data input and process were double tracked, and logic check was adopted.
Comparisons of essential features and living habits between cases and controls
Comparisons of general characteristics and living habits between cases and controls
χ 2 value
95 % CI
Number of subjects
Family history of tumors:
Total smoking amount:
Comparisons of genotypic polymorphisms between cases and controls
After analysis by Hardy–Weinberg test, all genotypic frequencies of three polymorphic sites in XRCC1 gene were ascertained in a balanced state in the Han population of China’s Jiangsu Province according to the heredity-balanced rule.
Comparison of genotypes of each polymorphic site between cases and controls
χ 2 value
95 % CI
Interaction between living habits and genetic polymorphisms in CRC risk
According to the results listed in Table 2, we set individuals with XRCC1 194Trp/Trp, 280Arg/Arg, or 399Arg/Arg genotype as the baseline for statistical analysis of interaction between living habits and genetic polymorphisms.
Influence of interaction between living habits and genetic polymorphisms on the risk of CRC
χ 2 value
95 % CI
Total smoking amount
Arg/Trp + Arg/Arg
Arg/Trp + Arg/Arg
Total smoking amount
Arg/His + His/His
Arg/His + His/His
Total smoking amount
Arg/Gln + Gln/Gln
Arg/Gln + Gln/Gln
Arg/Trp + Arg/Arg
Arg/His + His/His
Arg/Gln + Gln/Gln
Influence of genetic polymorphisms on the risk of CRC in smoking or drinking people
Controls (%) n = 350
Cases (%) n = 320
Arg/Trp + Arg/Arg
Arg/Gln + Gln/Gln
Arg/Gln + Gln/Gln
According to the epidemiological analysis of questionnaire data, we found that family history of tumors significantly increased the susceptibility of CRC, which showed the hereditary basis of patients with CRC, just like mostly tumorous patients. Although we did not find that only smoking habit increased significantly the risk of CRC, after stratification by total smoking amount, heavy smoking history significantly increased the susceptibility of CRC. It seemed that there lay a dosage–response relation during the process of cigarette carcinogenesis by the increased intake of reactive oxygen species and chemical carcinogens, such as olycyclic aromatic hydrocarbons, nitrosamines, and arylamines .
Abdel-Rahman et al. reported that XRCC1 399Gln allele might be associated with the increased risk for CRC in Egypt (OR = 3.98, 95 % CI 1.50–10.6) . In Korea, Hong et al. also discovered higher risk of 399Gln allele (OR = 1.61, 95 % CI 1.09–2.39) . Our results showed that the subjects with 399Arg/Trp (OR = 1.46, 95 % CI 1.06–2.01) or 399Trp/Trp genotype (OR = 1.93, 95 % CI 1.05–3.54) had a significantly increased risk for CRC, when compared with the individuals carrying 399Arg/Arg genotype of XRCC1 gene, which was consistent with the above-mentioned findings in Egypt and Korea. But, these findings were not proved in the studies conducted in a Norwegian population; Skjelbred et al. found that the XRCC1 399Gln allele was significantly associated with a reduction of CRC risk (OR = 0.62, 95 % CI 0.41–0.96) . It suggests that XRCC1 polymorphisms may play different roles in different populations and the precise mechanism needs further studies with more samples.
Human XRCC1 gene is mapped at human chromosome 19q13.2–13.3, spans a genomic distance 33 kb, contains 17 exons, and transcripts a protein of 633 amino acids (69.5 kDa) . In this study, we investigated the associations of three polymorphisms of the DNA repair gene XRCC1 with the risk of CRC in a southern Chinese population. The Arg399Gln polymorphism is located in the region of the breast cancer susceptibility gene C terminus I (BRCT-I) interaction domain of XRCC1 with poly(ADP-ribose) polymerase, and the presence of the variant 399Gln allele has been shown to be associated with measurable reduced DRC, as assessed by the persistence of DNA adducts [18, 19], tumor-suppressor gene P53 mutations , increased red blood cell glycophorin A , elevated levels of sister chromatid exchanges , and prolonged cell-cycle delay .
Both the XRCC1 Arg194Trp and Arg280His variants occur in the newly identified PCNA binding region . The XRCC1 Arg280His variant protein has an ineffective or reduced ability to localize a damaged site in the chromosome, thereby reducing the cellular BER/SSB repair efficiency. The variant 280His allele may allow un-repaired SSBs to accumulate, thereby accelerating genomic instability which consequently increases the risk of carcinogenesis . Only a few studies have investigated the association between the XRCC1 280His allele and risk of cancer. Skjelbred et al. in Norwegian found that 280His allele was significantly associated with an increased risk of colorectal adenomas (OR = 2.30, 95 % CI 1.19–4.46), but among the carcinoma cases, the same result was not observed (OR = 1.48, 95 % CI 0.29–7.48) . Also, no significant association has been observed with CRC in the study conducted by Hong et al. in a Korean population , and we also did not find significant association between the XRCC1 280His allele and colorectal carcinoma risk, which showed consistency with the result of Hong et al. in Asian people.
Few studies have examined the influence of the 194Trp allele on the function of the XRCC1 protein, but several researches have demonstrated same results in different populations. The study conducted by Abdel-Rahman et al. in Egypt showed that people with 194Trp allele did not tend to be in higher risk for CRC (OR = 2.56, 95 % CI 0.73–9.40) . Hong et al. in Korean  and Skjelbred et al. in Norwegian  also reported that XRCC1 194Trp allele did not significantly increase CRC risk. Our finding was also in accordance with the above-mentioned reports and showed that 194Arg/Trp and 194Trp/Trp genotypes both did not increase the risk for CRC when comparing with 194Arg/Arg genotype.
The XRCC1 protein plays a key role in base excision repair where it coordinates all the steps by serving as a scaffold via its interaction with other key base excision repair proteins, such as DNA polymerase β, DNA ligase III, polynucleotide kinase 3′-phosphatase, poly(ADP-ribose) polymerase, APE1, and OGG1. We analyzed the interaction of genetic polymorphisms of XRCC1 gene and unhealthy life habits, such as smoking and drinking habits, because many studies suggested that there lay widespread synergisms. A recent review of the literature found an overall modification of the effect of smoking by XRCC1 across several cancer types [24, 25]. So, the activity of XRCC1 protein is crucial to individuals to prevent the formation of mutations induced by chemical carcinogens in cigarette smoke. But, very few researches have discussed the interaction between smoking habit and XRCC1 genetic polymorphisms in CRC risk. In our results, there was no significant interaction between slight smoking history and all three genetic polymorphisms of XRCC1 gene after stratification by accumulative smoking amount, but we found that the individuals with heavy smoking history and 399Gln or 194Arg allele had significantly increased risk when compared with individuals who never smoked and carried 399Arg/Arg or 194Trp/Trp genotype, which seemed to be inconsistent with the finding observed by Stern et al. in Singapore Chinese. And, we did not do the associated analysis of haplotype and smoking habit because of the insufficient sample size. Besides, when we took XRCC1 399Gln allele or 194Arg allele into analysis for CRC in smoking or drinking population, it did not show significant relevance. This might also be because of the insufficient sample size.
Stern et al. in an American population found that the association between ever smoking and colorectal adenoma risk was only observed among subjects who carried the XRCC1 codon 194 Arg/Arg and codon 399 Arg/Arg or 399Arg/Gln genotypes (test of interaction, P = 0.048) . In Singapore Chinese, Stern et al. observed evidence that XRCC1 might modify the effects of smoking (interaction P = 0.012). The effect of smoking among carriers of the Arg(194)-Gln(399) haplotype was OR = 0.7 (95 % CI 0.4–1.1), whereas, among carriers of the Trp(194)-Arg(399) haplotype, it was OR = 1.6 (95 % CI 1.1–2.5) .
In addition, the interaction between three polymorphic sites of XRCC1 gene and drinking habit was also evaluated in this study, and it only showed a higher risk in subjects with 399Gln allele and drinking habit than individuals carrying 399Arg/Arg genotype but never drinking. Stern et al. in Singapore Chinese also observed a positive association between XRCC1 codon 194Trp/Trp genotype and alcohol consumption (OR = 2.8, 95 % CI 1.0–8.1), and thought a role for reactive oxygen species as relevant genotoxins that might account for the effects of both smoking and alcohol on colorectal cancer risk . Hong et al. found that alcohol consumption (≥80 g/week) is a significant risk factor of CRC (OR = 2.60, 95 % CI 1.46–4.62), but they did not analyze the interaction of XRCC1 polymorphisms and drinking habit . So, we considered that the decreased XRCC1 protein activity in response to chronic alcohol consumption probably finally contributed to the higher risk of CRC, though the mechanism was still not clear.
Taken together, the individuals, who are with XRCC1 194Arg allele and heavy smoking history, or who carry XRCC1 399Arg/Gln or 399Gln/Gln genotype and have a heavy smoking or drinking habit, have the increased risk for CRC in the population of Han nationality in Jiangsu Province of China which also shows a positive correlation with exposure dose of tobacco, but these XRCC1 polymorphisms could not be independent risk factors in smoking or drinking population. The etiology of CRC was unlikely to be explained only by genetic polymorphisms because hereditary variation, itself, could not affect the risk of any disease. Future molecular epidemiology studies should take more environmental risk factors into consideration for CRC.
This work was supported in part by the National Natural Science Foundation of China (81202077), “Qinglan” and “Six talent peaks” projects to Tiansong Xia, a project funded by the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD).
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Parkin DM. Global cancer statistics in the year 2000. Lancet Oncol. 2001;2:533–43.View ArticlePubMedGoogle Scholar
- Wang J, Gao Y, Wang L, Liu X, Li J, Wang Z, et al. A variant (rs932335) in the HSD11B1 gene is associated with colorectal cancer in a Chinese population. Eur J Cancer Prev. 2013;22:523–8.View ArticlePubMedGoogle Scholar
- Stern MC, Conti DV, Siegmund KD, Corral R, Yuan JM, Koh WP, et al. DNA repair single-nucleotide polymorphisms in colorectal cancer and their role as modifiers of the effect of cigarette smoking and alcohol in the Singapore Chinese Health Study. Cancer Epidemiol Biomarkers Prev. 2007;16:2363–72.View ArticlePubMedGoogle Scholar
- Stern MC, Siegmund KD, Conti DV, Corral R, Haile RW. XRCC1, XRCC3, and XPD polymorphisms as modifiers of the effect of smoking and alcohol on colorectal adenoma risk. Cancer Epidemiol Biomarkers Prev. 2006;15:2384–90.View ArticlePubMedGoogle Scholar
- Pryor WA. Cigarette smoke radicals and the role of free radicals in chemical carcinogenicity. Environ Health Perspect. 1997;105 Suppl 4:875–82.PubMed CentralView ArticlePubMedGoogle Scholar
- Brooks PJ, Theruvathu JA. DNA adducts from acetaldehyde: implications for alcohol-related carcinogenesis. Alcohol. 2005;35:187–93.View ArticlePubMedGoogle Scholar
- Seitz HK, Maurer B, Stickel F. Alcohol consumption and cancer of the gastrointestinal tract. Dig Dis. 2005;23:297–303.View ArticlePubMedGoogle Scholar
- Kubota Y, Nash RA, Klungland A, Schar P, Barnes DE, Lindahl T. Reconstitution of DNA base excision-repair with purified human proteins: interaction between DNA polymerase beta and the XRCC1 protein. EMBO J. 1996;15:6662–70.PubMed CentralPubMedGoogle Scholar
- Chen S, Tang D, Xue K, Xu L, Ma G, Hsu Y, et al. DNA repair gene XRCC1 and XPD polymorphisms and risk of lung cancer in a Chinese population. Carcinogenesis. 2002;23:1321–5.View ArticlePubMedGoogle Scholar
- Shen MR, Jones IM, Mohrenweiser H. Nonconservative amino acid substitution variants exist at polymorphic frequency in DNA repair genes in healthy humans. Cancer Res. 1998;58:604–8.PubMedGoogle Scholar
- Ye YN, Wu WK, Shin VY, Bruce IC, Wong BC, Cho CH. Dual inhibition of 5-LOX and COX-2 suppresses colon cancer formation promoted by cigarette smoke. Carcinogenesis. 2005;26:827–34.View ArticlePubMedGoogle Scholar
- Ye YN, Wu WK, Shin VY, Cho CH. A mechanistic study of colon cancer growth promoted by cigarette smoke extract. Eur J Pharmacol. 2005;519:52–7.View ArticlePubMedGoogle Scholar
- Xu Z, Hua LX, Qian LX, Yang J, Wang XR, Zhang W, et al. Relationship between XRCC1 polymorphisms and susceptibility to prostate cancer in men from Han, Southern China. Asian J Androl. 2007;9:331–8.View ArticlePubMedGoogle Scholar
- Abdel-Rahman SZ, Soliman AS, Bondy ML, Omar S, El-Badawy SA, Khaled HM, et al. Inheritance of the 194Trp and the 399Gln variant alleles of the DNA repair gene XRCC1 are associated with increased risk of early-onset colorectal carcinoma in Egypt. Cancer Lett. 2000;159:79–86.View ArticlePubMedGoogle Scholar
- Hong YC, Lee KH, Kim WC, Choi SK, Woo ZH, Shin SK, et al. Polymorphisms of XRCC1 gene, alcohol consumption and colorectal cancer. Int J Cancer. 2005;116:428–32.View ArticlePubMedGoogle Scholar
- Skjelbred CF, Saebo M, Wallin H, Nexo BA, Hagen PC, Lothe IM, et al. Polymorphisms of the XRCC1, XRCC3 and XPD genes and risk of colorectal adenoma and carcinoma, in a Norwegian cohort: a case control study. BMC Cancer. 2006;6:67.PubMed CentralView ArticlePubMedGoogle Scholar
- Mohrenweiser HW, Carrano AV, Fertitta A, Perry B, Thompson LH, Tucker JD, et al. Refined mapping of the three DNA repair genes, ERCC1, ERCC2, and XRCC1, on human chromosome 19. Cytogenet Cell Genet. 1989;52:11–4.View ArticlePubMedGoogle Scholar
- Lunn RM, Langlois RG, Hsieh LL, Thompson CL, Bell DA. XRCC1 polymorphisms: effects on aflatoxin B1-DNA adducts and glycophorin A variant frequency. Cancer Res. 1999;59:2557–61.PubMedGoogle Scholar
- Duell EJ, Wiencke JK, Cheng TJ, Varkonyi A, Zuo ZF, Ashok TD, et al. Polymorphisms in the DNA repair genes XRCC1 and ERCC2 and biomarkers of DNA damage in human blood mononuclear cells. Carcinogenesis. 2000;21:965–71.View ArticlePubMedGoogle Scholar
- Casse C, Hu YC, Ahrendt SA. The XRCC1 codon 399 Gln allele is associated with adenine to guanine p53 mutations in non-small cell lung cancer. Mutat Res. 2003;528:19–27.View ArticlePubMedGoogle Scholar
- Hu JJ, Smith TR, Miller MS, Lohman K, Case LD. Genetic regulation of ionizing radiation sensitivity and breast cancer risk. Environ Mol Mutagen. 2002;39:208–15.View ArticlePubMedGoogle Scholar
- Fan J, Otterlei M, Wong HK, Tomkinson AE, Wilson 3rd DM. XRCC1 co-localizes and physically interacts with PCNA. Nucleic Acids Res. 2004;32:2193–201.PubMed CentralView ArticlePubMedGoogle Scholar
- Takanami T, Nakamura J, Kubota Y, Horiuchi S. The Arg280His polymorphism in X-ray repair cross-complementing gene 1 impairs DNA repair ability. Mutat Res. 2005;582:135–45.View ArticlePubMedGoogle Scholar
- Hung RJ, Hall J, Brennan P, Boffetta P. Genetic polymorphisms in the base excision repair pathway and cancer risk: a HuGE review. Am J Epidemiol. 2005;162:925–42.View ArticlePubMedGoogle Scholar
- Caldecott KW. Protein-protein interactions during mammalian DNA single-strand break repair. Biochem Soc Trans. 2003;31:247–51.View ArticlePubMedGoogle Scholar