Genetic polymorphisms in the DNA repair gene XRCC1 and susceptibility to glioma in a Han population in northeastern China: A case-control study

Gene

Volumn 509, Issue 2, 2012, Pages 223-227

  Wang, Dianhong ^a   Hu, Yongzhen ^a   Gong, Haidong ^a   Li, Jingwen ^a   Ren, Yanhai ^b   Li, Guozhong ^a   Liu, Aiguo ^a  

^a THE FIRST AFFILIATED HOSPITAL OF HARBIN MEDICAL UNIVERSITY   (China)

^b Department of Neurosurgery   (China)

Author keywords

Case control study; Chinese; Glioma; Polymorphisms; SNP; XRCC1

Indexed keywords

ARGININE; GLUTAMINE; HISTONE; TRYPTOPHAN; XRCC1 PROTEIN;

ADULT; ARTICLE; CANCER PATIENT; CANCER RISK; CHINA; CONTROLLED STUDY; DNA REPAIR; FEMALE; GENE FREQUENCY; GENE LOCUS; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GENOTYPE; GLIOMA; HETEROZYGOTE; HOMOZYGOTE; HUMAN; MAJOR CLINICAL STUDY; MALE; POLYMERASE CHAIN REACTION; POPULATION; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SINGLE NUCLEOTIDE POLYMORPHISM; WILD TYPE;

ADOLESCENT; ADULT; ASIAN CONTINENTAL ANCESTRY GROUP; CASE-CONTROL STUDIES; CHINA; DNA REPAIR; DNA-BINDING PROTEINS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GLIOMA; HUMANS; MALE; MIDDLE AGED; POLYMERASE CHAIN REACTION; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; POLYMORPHISM, SINGLE NUCLEOTIDE; RISK FACTORS; YOUNG ADULT;

EID: 84866398606     PISSN: 03781119     EISSN: 18790038     Source Type: Journal    
DOI: 10.1016/j.gene.2012.08.023     Document Type: Article

References (29)

1. Audebert M., et al. Involvement of poly(ADP-ribose) polymerase-1 and XRCC1/DNA ligase III in an alternative route for DNA double-strand breaks rejoining. J. Biol. Chem. 2004, 279:55117-55126.
2. Bondy M.L., et al. Brain tumor epidemiology: consensus from the Brain Tumor Epidemiology Consortium. Cancer 2008, 113:1953-1968.
3. Butowski N.A., et al. Diagnosis and treatment of recurrent high-grade astrocytoma. J. Clin. Oncol. 2006, 24:1273-1280.
4. Felini M.J., et al. DNA repair polymorphisms XRCC1 and MGMT and risk of adult gliomas. Neuroepidemiology 2007, 29:55-58.
5. Fisher J.L., et al. Epidemiology of brain tumors. Neurol. Clin. 2007, 25:867-890. (vii).
6. Ginsberg G., et al. Polymorphism in the DNA repair enzyme XRCC1: utility of current database and implications for human health risk assessment. Mutat. Res. 2011, 727:1-15.
7. Horton J.K., et al. XRCC1 and DNA polymerase beta in cellular protection against cytotoxic DNA single-strand breaks. Cell Res. 2008, 18:48-63.
8. Hung R.J., et al. Genetic polymorphisms in the base excision repair pathway and cancer risk: a HuGE review. Am. J. Epidemiol. 2005, 162:925-942.
9. Inskip P.D., et al. Etiology of brain tumors in adults. Epidemiol. Rev. 1995, 17:382-414.
10. Jin L., Su B. Natives or immigrants: modern human origin in east Asia. Nat. Rev. Genet. 2000, 1:126-133.
11. Kiuru A., et al. XRCC1 and XRCC3 variants and risk of glioma and meningioma. J. Neurooncol. 2008, 88:135-142.
12. Laczmanska I., et al. Influence of polymorphisms in xenobiotic-metabolizing genes and DNA-repair genes on diepoxybutane-induced SCE frequency. Environ. Mol. Mutagen. 2006, 47:666-673.
13. Liu Y., et al. Tagging SNPs in non-homologous end-joining pathway genes and risk of glioma. Carcinogenesis 2007, 28:1906-1913.
14. Liu Y., et al. Polymorphisms of LIG4 and XRCC4 involved in the NHEJ pathway interact to modify risk of glioma. Hum. Mutat. 2008, 29:381-389.
15. Liu Y., et al. Association and interactions between DNA repair gene polymorphisms and adult glioma. Cancer Epidemiol. Biomarkers Prev. 2009, 18:204-214.
16. Mortusewicz O., Leonhardt H. XRCC1 and PCNA are loading platforms with distinct kinetic properties and different capacities to respond to multiple DNA lesions. BMC Mol. Biol. 2007, 8:81.
17. Parkin D.M., et al. Global cancer statistics, 2002. CA Cancer J. Clin. 2005, 55:74-108.
18. Pritchard J.K., Donnelly P. Case-control studies of association in structured or admixed populations. Theor. Popul. Biol. 2001, 60:227-237.
19. Purcell S., et al. Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits. Bioinformatics 2003, 19:149-150.
20. Rajaraman P., et al. DNA repair gene polymorphisms and risk of adult meningioma, glioma, and acoustic neuroma. Neuro Oncol. 2010, 12:37-48.
21. Ron E., et al. Tumors of the brain and nervous system after radiotherapy in childhood. N. Engl. J. Med. 1988, 319:1033-1039.
22. Sadetzki S., et al. Long-term follow-up for brain tumor development after childhood exposure to ionizing radiation for tinea capitis. Radiat. Res. 2005, 163:424-432.
23. Sterpone S., Cozzi R. Influence of XRCC1 genetic polymorphisms on ionizing radiation-induced DNA damage and repair. J. Nucleic Acids 2010, 6. (Article ID 780369). 10.4061/2010/780369.
24. Tebbs R.S., et al. Requirement for the Xrcc1 DNA base excision repair gene during early mouse development. Dev. Biol. 1999, 208:513-529.
25. Wang L.E., et al. Polymorphisms of DNA repair genes and risk of glioma. Cancer Res. 2004, 64:5560-5563.
26. Xu S., et al. Genomic dissection of population substructure of Han Chinese and its implication in association studies. Am. J. Hum. Genet. 2009, 85:762-774.
27. Yosunkaya E., et al. Glioma risk associates with polymorphisms of DNA repair genes, XRCC1 and PARP1. Br. J. Neurosurg. 2010, 24:561-565.
28. Zhou L.Q., et al. Polymorphisms of DNA Repair gene XRCC1 and Risk of Glioma: a case-control study in Southern China. Asian Pac. J. Cancer Prev. 2011, 12:2547-2550.
29. Zipprich J., et al. XRCC1 polymorphisms and breast cancer risk from the New York Site of the Breast Cancer Family Registry: a family-based case-control study. J. Carcinog. 2010, 9:4.