93
Views
10
CrossRef citations to date
0
Altmetric
Original Articles

Genotypic analysis of XRCC4 and susceptibility to cervical cancer

, , &
Pages 7-12 | Received 13 May 2019, Accepted 10 Jun 2019, Published online: 13 Aug 2019

References

  • Ferlay J, Ervik M, Lam F, et al. Global cancer observatory: cancer today. Lyon, France: International Agency for Research on Cancer; 2018 [Accessed on 23 May 2019]. Available from: https://gco.iarc.fr/today
  • Schiffman M, Castle PE. The promise of global cervical cancer prevention. New Engl J Med. 2005;353:2101–2104.
  • Hakem R. DNA-damage repair; the good, the bad, and the ugly. EMBO J. 2008;27:589–605.
  • Ferguson DO, Alt FW. DNA double strand break repair and chromosomal translocation: lessons from animal models. Oncogene. 2011;20:5572–5579.
  • Li Z, Otevrel T, Gao Y, et al. The XRCC4 gene encodes a novel protein involved in DNA double strand break repair and V(D)J recombination. Cell. 1995;83:1079–1089.
  • Critchlow SE, Bowater RP, Jackson SP. Mammalian DNA double-strand break repair protein XRCC4 interacts with DNA ligase IV. Curr Biol. 1997;7:588–598.
  • Chen L, Trujillo K, Sung P, et al. Interaction of the DNA ligase IV-XRCC4 complex with DNA ends and the DNA dependent protein kinase. J Biol Chem. 2000;275:26196–26205.
  • Gao Y, Ferguson DO, Xie W, et al. Interplay of p53 and DNA-repair protein XRCC4 in tumorigenesis, genomic stability and development. Nature. 2000;404:897–900.
  • Chang CH, Chang CL, Tsai CW, et al. Significant association of an XRCC4 single nucleotide polymorphism with bladder cancer susceptibility in Taiwan. Anticancer Res. 2009;29:1777–1782.
  • Chiu CF, Wang HC, Wang CH, et al. A new single nucleotide polymorphism in XRCC4 gene is associated with breast cancer susceptibility in Taiwanese patients. Anticancer Res. 2008;28:267–270.
  • Chiu CF, Wang CH, Wang CL, et al. A novel single nucleotide polymorphism in XRCC4 gene is associated with gastric cancer susceptibility in Taiwan. Ann Surg Oncol. 2008;15:514–518.
  • Chiu CF, Tsai MH, Tseng HC, et al. A novel single nucleotide polymorphism in XRCC4 gene is associated with oral cancer susceptibility in Taiwanese patients. Oral Oncol. 2008;44:898–902.
  • Bau DT, Yang MD, Tsou YA, et al. Colorectal cancer and genetic polymorphism of DNA double-strand break repair gene XRCC4 in Taiwan. Anticancer Res. 2010;30:2727–2730.
  • Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acid Res. 1988;16:1215.
  • Gautam S, Agrawal CG, Bid HK, et al. Preliminary studies on CD36 gene in type 2 diabetic patients from north India. Indian J Med Res. 2011;134:107–112.
  • Shi YY, He L. SHEsis is a powerful software platform for analyses of linkage disequilibrium, haplotype construction, and genetic association at polymorphism loci. Cell Res. 2005;15:97–98.
  • Abbas M, Srivastava K, Imran M, et al. Genetic polymorphisms in DNA repair genes and their association with cervical cancer. Br J Biomed Sci. 2019;14:1–5.
  • Anand P, Kunnumakara AB, Sundaram C, et al. Cancer is a preventable disease that requires major lifestyle changes. Pharm Res. 2008;25:2097–2116.
  • Mittal RD, Gangwar R, Mandal RK, et al. Gene variants of XRCC4 and XRCC3 and their association with risk for urothelial bladder cancer. Mol Biol Rep. 2012;39:1667–1675.
  • Zhou LP, Luan H, Dong XH, et al. Association of functional polymorphisms of the XRCC4 gene with the risk of breast cancer: a meta-analysis. Asian Pac J Cancer Prev. 2012;13:3431–3436.
  • Mandal RK, Singh V, Kapoor R, et al. Do polymorphisms in XRCC4 influence prostate cancer susceptibility in North Indian population? Biomarker. 2011;16:236–242.
  • Jung SW, Park NH, Shin JW, et al. Polymorphisms of DNA repair genes in Korean hepatocellular carcinoma patients with chronic hepatitis B: possible implications on survival. J Hepatol. 2012;57:621–627.
  • Long XD, Zhao D, Wang C, et al. Genetic polymorphisms in DNA repair genes XRCC4 and XRCC5 and aflatoxin B1-related hepatocellular carcinoma. Epidemiology. 2013;24:671–681.
  • Wang Y, Wang L, Li X, et al. Polymorphisms of XRCC4 are involved in reduced colorectal cancer risk in Chinese schizophrenia patients. BMC Cancer. 2010;10:523.
  • Kiyamova R, Garifulin O, Gryshkova V, et al. Preliminary study of thyroid and colon cancers-associated antigens and their cognate autoantibodies as potential cancer biomarkers. Biomarkers. 2012;17:362–371.
  • Yu H, Zhao H, Wang LE, et al. An analysis of single nucleotide polymorphisms of 125 DNA repair genes in the Texas genome-wide association study of lung cancer with a replication for the XRCC4 SNPs. DNA Repair. 2011;10:398–407.
  • Wu KH, Wang CH, Yang YL, et al. Significant association of XRCC4 single nucleotide polymorphisms with childhood leukemia in Taiwan. Anticancer Res. 2010;30:529–533.
  • Cifci S, Yilmaz M, Pehlivan M, et al. DNA repair genes polymorphisms in multiple myeloma: no association with XRCC1 (Arg399Gln) polymorphism, but the XRCC4 (VNTR in intron 3 and G-1394T) and XPD (Lys751Gln) polymorphisms is associated with the disease in Turkish patients. Hematology. 2011;16:361–367.
  • Shao N, Li J, Xu B, et al. Role of the functional variant (−652T>G) in the XRCC4 promoter in prostate cancer. Mol Biol Rep. 2014;41:7463–7470.
  • Hsu NY, Wang HC, Wang CH, et al. Lung cancer susceptibility and genetic polymorphism of DNA repair gene XRCC4 in Taiwan. Cancer Biomark. 2009;5:159–165.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.