Polymorphism of XRCC1 codon Arg 399 Gln is associated with higher susceptibility to endometriosis

Chinese Journal of Physiology

Volumn 50, Issue 6, 2007, Pages 326-329

  Bau, Da Tian ^a,b   Hsieh, Yao Yuan ^a   Wan, Lei ^a,b   Wang, Rou Fen ^a   Liao, Chiu Chu ^a   Lee, Cheng Chun ^a   Lin, Cheng Chieh ^a   Tsai, Chang Hai ^a   Tsai, Fuu Jen ^a,b  

^a CHINA MEDICAL UNIVERSITY HOSPITAL   (Taiwan)

^b CHINA MEDICAL UNIVERSITY   (Taiwan)

Author keywords

Arg399Gln; Endometriosis; Polymorphism; XRCC1

Indexed keywords

DNA; DNA BINDING PROTEIN; X-RAY REPAIR CROSS COMPLEMENTING PROTEIN 1; XRCC1 PROTEIN;

ADULT; ARTICLE; CODON; DNA REPAIR; ENDOMETRIOSIS; FEMALE; GENE FREQUENCY; GENETIC POLYMORPHISM; GENETICS; HUMAN; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; TAIWAN;

ADULT; CODON; DNA; DNA REPAIR; DNA-BINDING PROTEINS; ENDOMETRIOSIS; FEMALE; GENE FREQUENCY; HUMANS; POLYMORPHISM, GENETIC; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; TAIWAN;

EID: 44349089674     PISSN: 03044920     EISSN: 26660059     Source Type: Journal    
DOI: None     Document Type: Article

References (24)

1. Abdel-Rahman, S.Z. and El-Zein, R.A. The 399Gln polymorphism in the DNA repair gene XRCC1 modulates the genotoxic response induced in human lymphocytes by the tobacco-specific nitrosamine NNK. Cancer Lett. 159: 63-71, 2000.
2. Baranova, H., Bothorishvilli, R., Canis, M., Albuisson, E., Perriot, S., Glowaczower, E., Bruhat, M.A., Baranov, V. and Malet, P. Glutathione S-transferase M1 gene polymorphism and susceptibility to endometriosis in a French population. Mol. Hum. Reprod. 3: 775-780, 1997.
3. Bau, D.T., Fu, Y.P., Chen, S.T., Cheng, T.C., Yu, J.C., Wu, P.E. and Shen, C.Y. Breast cancer risk and the DNA double-strand break end-joining capacity of nonhomologous end-joining genes are affected by BRCA1. Cancer Res. 64: 5013-5019, 2004.
4. Bau, D.T., Mau, Y.C. and Shen, C.Y. The role of BRCA1 in nonhomologous end-joining. Cancer Lett. 240: 1-8, 2006.
5. Bischoff, F.Z. and Simpson, J.L. Heritability and molecular genetic studies of endometriosis. Hum. Reprod. Update 6: 37-44, 2000.
6. Bu, D., Tomlinson, G., Lewis, C.M., Zhang, C., Kildebeck, E. and Euhus, D.M. An intronic polymorphism associated with increased XRCC1 expression, reduced apoptosis and familial breast cancer. Breast Cancer Res. Treat. 99: 257-265, 2006.
7. Georgiou, I., Syrrou, M., Bouba, I., Dalkalitsis, N., Paschopoulos, M., Navrozoglou, I. and Lolis, D. Association of estrogen receptor gene polymorphisms with endometriosis. Fertil. Steril. 72: 164-166, 1999.
8. Heale, J.T., Ball, A.R., Jr., Schmiesing, J.A., Kim, J.S., Kong, X., Zhou, S., Hudson, D.F., Earnshaw, W.C. and Yokomori, K. Condensin I interacts with the PARP-1-XRCC1 complex and functions in DNA single-strand break repair. Mol. Cell 21: 837-848, 2006.
9. Hsieh, L.L., Chien, H.T., Chen, I.H., Liao, C.T., Wang, H.M., Jung, S.M., Wang, P.F., Chang, J.T., Chen, M.C. and Cheng, A.J. The XRCC1 399Gln polymorphism and the frequency of p53 mutations in Taiwanese oral squamous cell carcinomas. Cancer Epidemiol. Biomarkers Prev. 12: 439-443, 2003.
10. Hsieh, Y.Y., Chang, C.C., Tsai, F.J., Hsu, Y., Tsai, H.D. and Tsai, C.H. Polymorphisms for interleukin-4 (IL-4) -590 promoter, IL-4 intron3, and tumor necrosis factor alpha -308 promoter: nonassociation with endometriosis. J. Clin. Lab. Anal. 16: 121-126, 2002.
11. Hsieh, Y.Y., Chang, C.C., Tsai, F.J., Wu, J.Y., Shi, Y.R., Tsai, H.D. and Tsai, C.H. Polymorphisms for interleukin-1 beta (IL-1 beta)-511 promoter, IL-1 beta exon 5, and IL-1 receptor antagonist: nonassociation with endometriosis. J. Assist. Reprod. Genet. 18: 506-511, 2001.
12. Hsieh, Y.Y., Tsai, F.J., Chang, C.C., Chen, W.C., Tsai, C.H., Tsai, H.D. and Lin, C.C. p21 Gene codon 31 arginine/serine polymorphism: non-association with endometriosis. J. Clin. Lab. Anal. 15: 184-187, 2001.
13. Hu, J.J., Smith, T.R., Miller, M.S., Mohrenweiser, H.W., Golden, A. and Case, L.D. Amino acid substitution variants of APE1 and XRCC1 genes associated with ionizing radiation sensitivity. Carcinogenesis 22: 917-922, 2001.
14. Lamerdin, J.E., Montgomery, M.A., Stilwagen, S.A., Scheidecker, L.K., Tebbs, R.S., Brookman, K.W., Thompson, L.H. and Carrano, A.V. Genomic sequence comparison of the human and mouse XRCC1 DNA repair gene regions. Genomics 25: 547-554, 1995.
15. Lee, S.G., Kim, B., Choi, J., Kim, C., Lee, I. and Song, K. Genetic polymorphisms of XRCC1 and risk of gastric cancer. Cancer Lett. 187: 53-60, 2002.
16. 1 -DNA adducts and glycophorin A variant frequency. Cancer Res. 59: 2557-2561, 1999.
17. Mohrenweiser, H.W. and Jones, I.M. Variation in DNA repair is a factor in cancer susceptibility: a paradigm for the promises and perils of individual and population risk estimation? Mutat. Res. 400: 15-24, 1998.
18. Olshan, A.F., Watson, M.A., Weissler, M.C. and Bell, D.A. XRCC1 polymorphisms and head and neck cancer. Cancer Lett. 178: 181-186, 2002.
19. Qu, T., Morii, E., Oboki, K., Lu, Y. and Morimoto, K. Micronuclei in EM9 cells expressing polymorphic forms of human XRCC1. Cancer Lett. 221: 91-95, 2005.
20. Qu, T. and Morimoto, K. X-ray repair cross-complementing group 1 polymorphisms and cancer risks in Asian populations: a mini review. Cancer Detect. Prev. 29: 215-220, 2005.
21. Ramachandran, S., Ramadas, K., Hariharan, R., Rejnish, K.R. and Radhakrishna, P.M. Single nucleotide polymorphisms of DNA repair genes XRCC1 and XPD and its molecular mapping in Indian oral cancer. Oral Oncol. 42: 350-362, 2006.
22. Shen, H., Xu, Y., Qian, Y., Yu, R., Qin, Y., Zhou, L., Wang, X., Spitz, M.R. and Wei, Q. Polymorphisms of the DNA repair gene XRCC1 and risk of gastric cancer in a Chinese population. Int. J. Cancer 88: 601-606, 2000.
23. Shen, M.R., Zdzienicka, M.Z., Mohrenweiser, H., Thompson, L.H. and Thelen, M.P. Mutations in hamster single-strand break repair gene XRCC1 causing defective DNA repair. Nucleic Acids Res. 26: 1032-1037, 1998.
24. Smith, T.R., Miller, M.S., Lohman, K., Lange, E.M., Case, L.D., Mohrenweiser, H.W. and Hu, J.J. Polymorphisms of XRCC1 and XRCC3 genes and susceptibility to breast cancer. Cancer Lett. 190: 183-190, 2003.