J Korean Med Sci.  2011 Aug;26(8):991-995. 10.3346/jkms.2011.26.8.991.

XRCC1 Polymorphisms and Risk of Papillary Thyroid Carcinoma in a Korean Sample

Affiliations
  • 1Department of Otolaryngology-Head and Neck Surgery, Hanyang University School of Medicine, Seoul, Korea. kytae@hanyang.ac.kr
  • 2Department of Internal Medicine, Hanyang University School of Medicine, Seoul, Korea.

Abstract

Polymorphisms of DNA repair genes, X-ray repair cross-complementing group 1 (XRCC1) might contribute to individual susceptibility to different types of cancers. We analyzed the relationship between XRCC1 polymorphisms and the risk of papillary thyroid carcinoma in a Korean sample. A hospital-based case-control study was performed in 111 papillary thyroid carcinoma patients and 100 normal control subjects. XRCC1 Arg194Trp and Arg399Gln single nucleotide polymorphisms (SNPs) were genotyped by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). The XRCC1 Arg194Trp Arg/Trp genotype was significantly associated with a decreased risk of papillary thyroid carcinoma compared to that of Arg/Arg genotype (odds ratio [95% confidence intervals]; 0.550 [0.308-0.983]). There was no significant association between XRCC1 Arg399Gln genotypes and risk of papillary thyroid carcinoma. Based on these results, the XRCC1 Arg194Trp Arg/Trp genotype could be used as a useful molecular biomarker to predict genetic susceptibility for papillary thyroid carcinoma in Koreans.

Keyword

Polymorphisms; XRCC1; SNP; Papillary Thyroid Carcinoma; Susceptibility

MeSH Terms

Adolescent
Adult
Aged
Aged, 80 and over
Amino Acid Substitution
Asian Continental Ancestry Group/*genetics
Case-Control Studies
DNA-Binding Proteins/*genetics
Female
Genetic Predisposition to Disease
Genotype
Humans
Male
Middle Aged
Odds Ratio
Polymorphism, Single Nucleotide
Republic of Korea
Risk Factors
Thyroid Neoplasms/*genetics

Figure

  • Fig. 1 XRCC1 Arg194Trp single nucleotide polymorphism (SNP) by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). Arg/Arg genotype, lane 1 and 3; Arg/Trp genotype, lane 2 and 4; Trp/Trp genotype, lane 5.

  • Fig. 2 XRCC1 Arg399Gln single nucleotide polymorphism (SNP) by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). Arg/Arg genotype, lane 1; Arg/Gln genotype, lane 3 and 4; Gln/Gln genotype, lane 2.


Reference

1. How J, Tabah R. Explaining the increasing incidence of differentiated thyroid cancer. CMAJ. 2007. 177:1383–1384.
2. Jung KW, Park S, Kong HJ, Won YJ, Boo YK, Shin HR, Park EC, Lee JS. Cancer statistics in Korea: incidence, mortality and survival in 2006-2007. J Korean Med Sci. 2010. 25:1113–1121.
3. Shore RE. Issues and epidemiological evidence regarding radiation-induced thyroid cancer. Radiat Res. 1992. 131:98–111.
4. Spitz MR, Fueger JJ, Beddingfield NA, Annegers JF, Hsu TC, Newell GR, Schantz SP. Chromosome sensitivity to bleomycin-induced mutagenesis, an independent risk factor for upper aerodigestive tract cancers. Cancer Res. 1989. 49:4626–4628.
5. Wang LE, Sturgis EM, Eicher SA, Spitz MR, Hong WK, Wei Q. Mutagen sensitivity to benzo(a)pyrene diol epoxide and the risk of squamous cell carcinoma of the head and neck. Clin Cancer Res. 1998. 4:1773–1778.
6. Cheng L, Eicher SA, Guo Z, Hong WK, Spitz MR, Wei Q. Reduced DNA repair capacity in head and neck cancer patients. Cancer Epidemiol Biomarkers Prev. 1998. 7:465–468.
7. Schantz SP, Hsu TC, Ainslie N, Moser RP. Young adults with head and neck cancer express increased susceptibility to mutagen-induced chromosome damage. JAMA. 1989. 262:3313–3315.
8. Tae K, Lee HS, Park BJ, Park CW, Kim KR, Cho HY, Kim LH, Park BL, Shin HD. Association of DNA repair gene XRCC1 polymorphisms with head and neck cancer in Korean population. Int J Cancer. 2004. 111:805–808.
9. Ji YB, Tae K, Lee YS, Lee SH, Kim KR, Park CW, Park BL, Shin HD. XPD polymorphisms and risk of squamous cell carcinoma of the head and neck in a Korean sample. Clin Exp Otorhinolaryngol. 2010. 3:42–47.
10. Hu JJ, Mohrenweiser HW, Bell DA, Leadon SA, Miller MS. Symposium overview: genetic polymorphisms in DNA repair and cancer risk. Toxicol Appl Pharmacol. 2002. 185:64–73.
11. Kubota Y, Nash RA, Klungland A, Schär P, Barnes DE, Lindahl T. Reconstruction of DNA base excision-repair with purified human proteins: interaction between DNA polymerase beta and the XRCC1 protein. EMBO J. 1996. 15:6662–6670.
12. Izumi T, Hazra TK, Boldogh I, Tomkinson AE, Park MS, Ikeda S, Mitra S. Requirement for human AP endonuclease 1 for repair of 3'-blocking damage at DNA single-strand breaks induced by reactive oxygen species. Carcinogenesis. 2000. 21:1329–1334.
13. Zhang X, Moréra S, Bates PA, Whitehead PC, Coffer AI, Hainbucher K, Nash RA, Sternberg MJ, Lindahl T, Freemont PS. Structure of an XRCC1 BRCT domain: a new protein-protein interaction module. EMBO J. 1998. 17:6404–6411.
14. Vidal AE, Boiteux S, Hickson ID, Radicella JP. XRCC1 coordinates the initial and late stages of DNA abasic site repair through protein-protein interaction. EMBO J. 2001. 20:6530–6539.
15. Patel AV, Calle EE, Pavluck AL, Feigelson HS, Thun MJ, Rodriguez C. A prospective study of XRCC1 (X-ray cross-complementing group 1) polymorphisms and breast cancer risk. Breast Cancer Res. 2005. 7:R1168–R1173.
16. Wang Y, Yang H, Li H, Li L, Wang H, Liu C, Zheng Y. Association between X-ray repair cross complementing group 1 codon 399 and 194 polymorphisms and lung cancer risk: a meta-analysis. Cancer Lett. 2009. 285:134–140.
17. Dai L, Wang K, Zhang J, Lv Q, Wu X, Wang Y. XRCC1 gene polymorphisms and esophageal squamous cell carcinoma risk in Chinese population: a meta-analysis of case-control studies. Int J Cancer. 2009. 125:1102–1109.
18. Shen H, Xu Y, Qian Y, Yu R, Qin Y, Zhou L, Wang X, Spitz MR, Wei Q. Polymorphisms of the DNA repair gene XRCC1 and risk of gastric cancer in a Chinese population. Int J Cancer. 2000. 88:601–606.
19. Chiang FY, Wu CW, Hsiao PJ, Kuo WR, Lee KW, Lin JC, Liao YC, Juo SH. Association between polymorphism in DNA base excision repair genes XRCC1, APE1, and ADPRT and differentiated thyroid carcinoma. Clin Cancer Res. 2008. 14:5919–5924.
20. Ho T, Li G, Lu J, Zhao C, Wei Q, Sturgis EM. Association of XRCC1 polymorphisms and risk of differentiated thyroid carcinoma: a case-control analysis. Thyroid. 2009. 19:129–135.
21. Zhu QX, Bian JC, Shen Q, Jiang F, Tang HW, Zhang HW, Wu Y. Genetic polymorphisms in X-ray repair cross-complementing gene 1 and susceptibility to papillary thyroid carcinoma. Zhonghua Liu Xing Bing Xue Za Zhi. 2004. 25:702–705.
22. Sigurdson AJ, Land CE, Bhatti P, Pineda M, Brenner A, Carr Z, Gusev BI, Zhumadilov Z, Simon SL, Bouville A, Rutter JL, Ron E, Struewing JP. Thyroid nodule, polymorphic variants in DNA repair and RET-related genes, and interaction with ionizing radiation exposure from nuclear tests in Kazakhstan. Radiat Res. 2009. 171:77–88.
Full Text Links
  • JKMS
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr