Log in

DNA repair XPCC1 and XPD genes polymorphism as associated with the development of bladder cancer and renal cell carcinoma

  • Human Genetics
  • Published:
Russian Journal of Genetics Aims and scope Submit manuscript

Abstract

We examined the associations between the polymorphic alleles of the DNA repair genes XRCC1 (c.839G>A, rs25489; and c.1196A>G, rs25487), XPA (c.-4A>G, rs1800975), and XPD (c.2251A>C, rs13181) and the progression and severity of neoplasias in the urinary bladder and kidney in patients of three distinct ethnic groups, Bashkir, Russians, and Tatar, residing in the Republic of Bashkorostan. The study enrolled 468 cancer patients and 351 healthy individuals. Genoty** for polymorphic alleles was carried out using the PCR-RFLP method. We identified an association between allele A of the c.839G>A locus of the XRCC1 gene and the incidence of the bladder cancer (BC) and renal cell carcinoma (RCC) in the Tatar study group, using the additive genetic effects model (Odds Ratio (OR) = 5.23 and OR = 3.90). In turn, the heterozygous G/A genotype frequency was significantly higher in the RCC patients of Bashkir ethnic origin, compared with the control group (p = 0.0061, OR = 4.72). Additional analysis with consideration of participants smoking status showed that the G/A genotype is significantly more frequent in smokers with BC (OR = 1.96, p = 0.05) than in healthy smokers. We also determined, using the recessive genetic model, that the genotype A/A of the c.1196A>G locus of the XRCC1 gene was associated with a higher risk of BC in the Russian cohort (OR = 2.29, p = 0.0082) and an increased incidence of RCC in the Bashkir group (OR = 4.06, p = 0.05). A similar association was obtained for smokers. In contrast, the allele c.2251A>C in the XPD gene associated with a lower risk for BC and RCC in the Tatars (p = 0.0003, OR = 0.48 and p < 0.0001, OR = 0.37) in the additive model and in the Bashkirs (p = 0.0083, OR = 0.12) and Russians (p = 0.0001, OR = 0.14) in the recessive model. Further, we uncovered that polymorphism c.839G>A in the XRCC1 gene contributes to the progression of noninvasive and invasive BC and promotes RCC at early and advanced stages of the disease. Thus, we identified similar associations between DNA repair gene polymorphisms and the incidence and progression of BC and RCC. We propose that this result points to the involvement of common pathogenetic mechanisms in the initiation and progression of the urinary neoplasias.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Subscribe and save

Springer+ Basic
EUR 32.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or Ebook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

Price includes VAT (Germany)

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. GLOBOCAN 2002. http://www.dep.iarc.fr/globocan/globocan.htm

  2. European Association of Urology: Guidelines, 2013.

  3. Glantz, S.A., Primer of Biostatistics New York: McGraw-Hill, 1997, 4th ed.

    Google Scholar 

  4. Rodriguez, S., Gaunt, T.R., and Day, I.N.M., Hardy-Weinberg equilibrium testing of biological ascertainment for Mendelian randomization studies, Am. J. Epidemiol. Adv., 2009. doi 10.1093/aje/kwn359

    Google Scholar 

  5. SNPStats. http://bioinfo.iconcologia.net/SNPstats-web

  6. Kochetova, O.V., Korytina, G.F., Akhmadishina, L.Z., and Victorova, T.V., Polymorphisms of DNA repair genes (XRCC1, XRCC3, XPC, XPD, XPA) in ethnic groups from republic of Bashkortostan, Russ. J. Genet., 2013, vol. 49, no. 8, pp. 870–876.

    Article  CAS  Google Scholar 

  7. Rakitin, S.S., Dmitrieva, A.I., Novitskii, V.V., et al., Genetic polymorphism of the DNA reparation system among gastric cancer patients with different histological tumor types, Fundam. Issled., 2011, no. 3, pp. 125–130.

    Google Scholar 

  8. Ladige, W.C., Mouse models of XRCC1 DNA repair polymorphisms and cancer, Oncogene, 2006, no. 25, pp. 1612–1619.

    Google Scholar 

  9. Mao, Y., Xu, X., Lin, Y., et al., Quantitative assessment of the associations between XRCC1 polymorphisms and BC risk, World J. Surg. Oncol., 2013, vol. 11, no. 58. http://www.wjso.com/content/11/1/58

    Google Scholar 

  10. Zhang, K., Zhou, B., Wang, Y., et al., The XRCC1 Arg280His polymorphism contributes to cancer susceptibility: an update by meta-analysis of 53 individual studies, Gene, 2012, no. 510, pp. 93–101.

    Google Scholar 

  11. Zhuo, W., Zhang, L., Cai, L., et al., XRCC1 Arg280His polymorphism and BC risk: updated meta-analyses based on 5767 cases and 6919 controls, Exp. Biol. Med., 2013, vol. 238, no. 1, pp. 66–76.

    Article  CAS  Google Scholar 

  12. Hirata, H., Hinoda, Y., Matsuyama, H., et al., Polymorphisms of DNA repair genes are associated with renal cell carcinoma, Biochem. Biophys. Res. Commun., 2006, vol. 342, no. 4, pp. 1058–1062.

    Article  CAS  PubMed  Google Scholar 

  13. Sakano, S., Hinoda, Y., Okayama, N., et al., The association of DNA repair gene polymorphisms with the development and progression of renal cell carcinoma, Ann. Oncol., 2007, vol. 18, no. 11, pp. 1817–1827.

    Article  CAS  PubMed  Google Scholar 

  14. Benhamoul, S. and Sarasin, A., ERCC2/XPD gene polymorphisms and lung cancer: a huge review, Am. J. Epidemiol., 2005, no. 161, pp. 1–14.

    Google Scholar 

  15. http://www.ncbi.nlm.nih.gov/snp

  16. Tiseo, M., Bordi, P., Bortesi, B., et al., ERCC1/BRCA1 expression and gene polymorphisms as prognostic and predictive factors in advanced NSCLC treated with or without cisplatin, Br. J. Cancer, 2013. doi: 10.1038/bjc.2013.127

    Google Scholar 

  17. Wang, M., Gu, D., Zhang, Z., et al., XPD polymorphisms, cigarette smoking, and BC risk: a meta-analysis, J. Toxicol. Environ. Health A, 2009, vol. 72, nos. 11–12, pp. 698–705.

    Article  CAS  PubMed  Google Scholar 

  18. Sobti, R.C., Kaur, S., Sharma, V.L., et al., Susceptibility of XPD and RAD51 genetic variants to carcinoma of urinary bladder in North Indian population, DNA Cell Boil., 2012, vol. 31, no. 2, pp. 199–210.

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to L. Z. Akhmadishina.

Additional information

Original Russian Text © L.Z. Akhmadishina, I.R. Gilyazova, L.R. Kutlyeva, G.F. Korytina, O.V. Kochetova, M.F. Urmantsev, S.M. Izmailova, A.A. Izmailov, G.B. Kunsbaeva, A.A. Zagidullin, A.A. Khaliullin, V.N. Pavlov, T.V. Victorova, E.K. Khusnutdinova, 2014, published in Genetika, 2014, Vol. 50, No. 4, pp. 481–490.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Akhmadishina, L.Z., Gilyazova, I.R., Kutlyeva, L.R. et al. DNA repair XPCC1 and XPD genes polymorphism as associated with the development of bladder cancer and renal cell carcinoma. Russ J Genet 50, 421–429 (2014). https://doi.org/10.1134/S1022795414040024

Download citation

  • Received:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1134/S1022795414040024

Keywords

Navigation