DOI QR코드

DOI QR Code

Comprehensive Study on Associations Between Nine SNPs and Glioma Risk

  • Liu, Hai-Bo (Department of Neurosurgery, the Affiliated Nanfang Hospital of Southern Medical University) ;
  • Peng, Yu-Ping (Department of Neurosurgery, the Affiliated Nanfang Hospital of Southern Medical University) ;
  • Dou, Chang-Wu (Department of Neurosurgery, the Affiliated Hospital of Inner Mongolia Medical University) ;
  • Su, Xiu-Lan (Central Laboratory, the Affiliated Hospital of Inner Mongolia Medical University) ;
  • Gao, Nai-Kang (Department of Neurosurgery, the Affiliated Hospital of Inner Mongolia Medical University) ;
  • Tian, Fu-Ming (Department of Neurosurgery, the Affiliated Hospital of Inner Mongolia Medical University) ;
  • Bai, Jie (Department of Neurosurgery, the Affiliated Hospital of Inner Mongolia Medical University)
  • Published : 2012.10.31

Abstract

Aim: Glioma cancer is the most common type of adult brain tumor. Recent genome-wide association studies (GWAS) have identified various new susceptibility regions and here we conducted an extensive analysis of associations between 12 single nucleotide polymorphisms (SNPs) and glioma risk. Methods: A total of 197 glioma cases and 197 health controls were selected, and 9 SNPs in 8 genes were analyzed using the Sequenom MassARRAY platform and Sequenom Assay Design 3.1 software. Results: We found the MAF among selected controls were consistent with the MAF from the NCBI SNP database. Among 9 SNPs in 8 genes, we identified four significant SNP genotypes associated with the risk of glioma, C/C genotype at rs730437 and T/T genotype at rs1468727 in ERGF were protective against glioma, whereas the T/T genotype at rs1799782 in XRCC1 and C/C genotype at rs861539 in XRCC3 conferred elevated risk. Conclusion: Our comprehensive analysis of nine SNPs in eight genes suggests that the rs730437 and rs1468727 in ERGF, rs1799782 in XRCC1 gene, and rs861539 in XRCC3 gene are associated with glioma risk. These findings indicate that genetic variants of various genes play a complex role in the development of glioma.

Keywords

References

  1. Andersson U, Schwartzbaum J, Wiklund F, et al (2010). A comprehensive study of the association between the EGFR and ERBB2 genes and glioma risk. Acta Oncol, 49, 767-75. https://doi.org/10.3109/0284186X.2010.480980
  2. Bondy ML, Scheurer ME, Malmer B, et al (2008). Brain tumor epidemiology: consensus from the Brain Tumor Epidemiology Consortium. Cancer, 113, 1953-68. https://doi.org/10.1002/cncr.23741
  3. Custodio AC, Almeida LO, Pinto GR, et al (2011). Analysis of the polymorphisms XRCC1Arg194Trp and XRCC1Arg399Gln in gliomas. Genet Mol Res, 10, 1120-9. https://doi.org/10.4238/vol10-2gmr1125
  4. Felini MJ, Olshan AF, Schroeder JC, et al (2007). DNA repair polymorphisms XRCC1 and MGMT and risk of adult gliomas. Neuroepidemiology, 29, 55-8. https://doi.org/10.1159/000108919
  5. Gabriel S, Ziaugra L, Tabbaa D (2009). SNP genotyping using the Sequenom MassARRAY iPLEX platform. Current Protocols in Human Genetics, Chapter 2, Unit 2, 12.
  6. Kiuru A, Lindholm C, Heinävaara S, et al (2008). XRCC1 and XRCC3 variants and risk of glioma and meningioma. J Neurooncol, 88, 135-42. https://doi.org/10.1007/s11060-008-9556-y
  7. Kharrat N, Al'Fadhli S, Rebai M, et al (2007). (AC) dinucleotide repeat polymorphism in intron 1 of human EGFR shows ethnic specificities and high evidence for association with breast cancer. Int J Biol Markers, 22, 258-64.
  8. Han B, Zhou X, Zhang RX, et al. Mutations of the epidermal growth factor receptor gene in NSCLC patients. Oncol Lett, 2, 1233-7.
  9. Hedman H, Henriksson R (2007). LRIG inhibitors of growth factor signallingdouble- edged swords in human cancer? Eur J Cancer, 43, 676-82. https://doi.org/10.1016/j.ejca.2006.10.021
  10. He SY, Xu L, Niu G, et al (2012). Predictive Value of Excision Repair Cross-complementing Rodent Repair Deficiency Complementation Group 1 and Ovarian Cancer Risk. Asian Pac J Cancer Prev, 13, 1799-802. https://doi.org/10.7314/APJCP.2012.13.5.1799
  11. Hou WG, Ai WB, Bai XG, et al(2012). Genetic variation in the EGFR gene and the risk of glioma in a Chinese Han population. PLoS ONE, 7, e37531. https://doi.org/10.1371/journal.pone.0037531
  12. Hu XB, Feng Z, Fan YC, et al (2011). Polymorphisms in DNA repair gene XRCC1 and increased genetic susceptibility to glioma. Asian Pac J Cancer Prev, 12, 2981-4.
  13. Lee SA, Lee KM, Park SK, et al (2007). Genetic polymorphism of XRCC3 Thr241Met and breast cancer risk: case-control study in Korean women and meta-analysis of 12 studies. Breast Cancer Res Treat, 103, 71-6. https://doi.org/10.1007/s10549-006-9348-z
  14. Liu Y, Chen H, Chen L, et al (2012). Prediction of genetic polymorphisms of DNA repair genes XRCC1 and XRCC3 in the survival of colorectal cancer receiving chemotherapy in the Chinese population. Hepatogastroenterology, 59, 977-80.
  15. McWilliams RR, Bamlet WR, Cunningham JM, et al (2008). Polymorphisms in DNA repair genes, smoking, and pancreatic adenocarcinoma risk. Cancer Res, 68, 4928-35. https://doi.org/10.1158/0008-5472.CAN-07-5539
  16. Parkin DM, Bray F, Ferlay J, et al (2005) Global cancer statistics, 2002. CA Cancer J Clin, 55, 74-108. https://doi.org/10.3322/canjclin.55.2.74
  17. Perez CA, Chen H, Shyr Y, et al (2010). The EGFR polymorphism rs884419 is associated with freedom from recurrence in patients with resected prostate cancer. J Urol, 183, 2062-9. https://doi.org/10.1016/j.juro.2009.12.098
  18. Rajaraman P, Melin BS, Wang Z, et al (2012). Genome-wide association study of glioma and meta-analysis. Hum Genet.
  19. Sadetzki S, Chetrit A, Freedman L, et al (2005). Long-term follow-up for brain tumor development after childhood exposure to ionizing radiation for tinea capitis. Radiat Res, 164, 424-32.
  20. Sreeja L, Syamala VS, Syamala V, et al (2008). Prognostic importance of DNA repair gene polymorphisms of XRCC1 Arg399Gln and XPD Lys751Gln in lung cancer patients from India. J Cancer Res Clin Oncol, 134, 645-52. https://doi.org/10.1007/s00432-007-0328-4
  21. Thomas RK, Baker AC, Debiasi RM, et al (2007). High-throughput oncogene mutation profiling in human cancer. Nature Genetics, 39, 347-51. https://doi.org/10.1038/ng1975
  22. Tokunaga A, Onda M, Okuda T, et al (1995). Clinical significance of epidermal growth factor (EGF), EGF receptor, and c-erbB-2 in human gastric cancer. Cancer, 75, 1418-25. https://doi.org/10.1002/1097-0142(19950315)75:6+<1418::AID-CNCR2820751505>3.0.CO;2-Y
  23. Upadhyay R, Jain M, Kumar S, et al (2008). Interaction of EGFR 497Arg.Lys with EGF +61A.G polymorphism: modulation of risk in esophageal cancer. Oncol Res, 17, 167-74. https://doi.org/10.3727/096504008785114147
  24. Wrensch M, Jenkins RB, Chang JS, et al (2009). Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility. Nature Genetics, 41, 905-8. https://doi.org/10.1038/ng.408
  25. Wang N, Wu Y, Zhou X, et al (2012). Association between genetic polymorphism of metabolizing enzymes and DNA repairing enzymes and the susceptibility of lung cancer in Henan population. Wei Sheng Yan Jiu, 41, 251-6.
  26. Wen YY, Pan XF, Loh M, et al (2012). ADPRT Val762Ala and XRCC1 Arg194Trp Polymorphisms and Risk of Gastric Cancer in Sichuan of China. Asian Pac J Cancer Prev, 13, 2139-44. https://doi.org/10.7314/APJCP.2012.13.5.2139
  27. Wong AJ, Ruppert JM, Bigner SH, et al (1992). Structural alterations of the epidermal growth factor receptor gene in human gliomas. Proc Natl Acad Sci U S A, 89, 2965-9. https://doi.org/10.1073/pnas.89.7.2965
  28. Wrensch M, Kelsey KT, Liu M, et al(2004). Glutathione-Stransferase variants and adult glioma. Cancer Epidemiol Biomarkers Prev, 13, 461-7.
  29. Yao L, Ji G, Gu A, et al(2012). An updated pooled analysis of glutathione S-transferase genotype polymorphisms and risk of adult gliomas. Asian Pac J Cancer Prev, 13, 157-63. https://doi.org/10.7314/APJCP.2012.13.1.157
  30. Yun J, Song SH, Park J, et al (2012). Gene silencing of EREG mediated by DNA methylation and histone modification in human gastric cancers. Lab Invest, 92, 1033-44. https://doi.org/10.1038/labinvest.2012.61
  31. Zhao Y, Deng X, Wang Z, et al (2012). Genetic polymorphisms of DNA repair genes XRCC1 and XRCC3 and risk of colorectal cancer in Chinese population. Asian Pac J Cancer Prev, 13, 665-9. https://doi.org/10.7314/APJCP.2012.13.2.665
  32. Zhou LQ, Ma Z, Shi XF, et al (2011). Polymorphisms of DNA repair gene XRCC1 and risk of glioma: a case-control study in Southern China. Asian Pac J Cancer Prev, 12, 2547-50.

Cited by

  1. Association Between Genetic Polymorphism of XRCC1 Gene and Risk of Glioma in а Chinese Population vol.14, pp.10, 2013, https://doi.org/10.7314/APJCP.2013.14.10.5957
  2. The XRCC3 Thr241Met Polymorphism Influences Glioma Risk - A Meta-analysis vol.14, pp.5, 2013, https://doi.org/10.7314/APJCP.2013.14.5.3169
  3. Xeroderma Pigmentosum Complementation Group F Polymorphisms Influence Risk of Glioma vol.14, pp.7, 2013, https://doi.org/10.7314/APJCP.2013.14.7.4083
  4. Association of XRCC3 Thr241Met Polymorphisms and Gliomas Risk: Evidence from a Meta-analysis vol.14, pp.7, 2013, https://doi.org/10.7314/APJCP.2013.14.7.4243
  5. Associations between three XRCC1 polymorphisms and glioma risk: a meta-analysis vol.34, pp.5, 2013, https://doi.org/10.1007/s13277-013-0865-1
  6. Fatty Acid Synthesis Pathway Genetic Variants and Clinical Outcome of Non-Small Cell Lung Cancer Patients after Surgery vol.15, pp.17, 2014, https://doi.org/10.7314/APJCP.2014.15.17.7097
  7. Association between the XRCC1 Arg194Trp Polymorphism and Glioma Risk: an Updated Meta-analysis vol.15, pp.17, 2014, https://doi.org/10.7314/APJCP.2014.15.17.7419
  8. Genetic polymorphisms in XRCC1 gene and susceptibility to glioma in Chinese Han population vol.35, pp.1, 2014, https://doi.org/10.1007/s13277-013-1050-2
  9. Association between the Thr241Met polymorphism of X-ray repair cross-complementing group 3 gene and glioma risk: evidence from a meta-analysis based on 4,136 cases and 5,233 controls vol.35, pp.1, 2014, https://doi.org/10.1007/s13277-013-1059-6
  10. Association between the XRCC1 Arg194Trp polymorphism and risk of cancer: evidence from 201 case–control studies vol.35, pp.11, 2014, https://doi.org/10.1007/s13277-014-2326-x
  11. Association between XRCC3 Thr241Met polymorphism and risk of brain tumors: a meta-analysis vol.35, pp.2, 2014, https://doi.org/10.1007/s13277-013-1144-x
  12. Quantitative assessment of the association between XRCC3 C18607T polymorphism and glioma risk vol.35, pp.2, 2014, https://doi.org/10.1007/s13277-013-1147-7
  13. Association between XRCC3 T241M polymorphism and glioma risk: a meta-analysis vol.35, pp.6, 2014, https://doi.org/10.1007/s13277-014-1738-y
  14. XRCC1 Gene Polymorphisms and Glioma Risk in Chinese Population: A Meta-Analysis vol.9, pp.11, 2014, https://doi.org/10.1371/journal.pone.0111981
  15. Association between the TERT Genetic Polymorphism rs2853676 and Cancer Risk: Meta-Analysis of 76 108 Cases and 134 215 Controls vol.10, pp.6, 2015, https://doi.org/10.1371/journal.pone.0128829
  16. Polymorphisms in Genes of the De Novo Lipogenesis Pathway and Overall Survival of Hepatocellular Carcinoma Patients Undergoing Transarterial Chemoembolization vol.16, pp.3, 2015, https://doi.org/10.7314/APJCP.2015.16.3.1051
  17. Effect of thymidylate synthase gene polymorphism on the response to chemotherapy and clinical outcome of non-small cell lung cancer patients vol.36, pp.9, 2015, https://doi.org/10.1007/s13277-015-3447-6
  18. Global incidence of malignant brain and other central nervous system tumors by histology, 2003–2007 vol.19, pp.11, 2017, https://doi.org/10.1093/neuonc/nox091
  19. A Comprehensive Meta-analysis of Genetic Associations Between Key Polymorphic Loci in DNA Repair Genes and Glioma Risk vol.54, pp.2, 2017, https://doi.org/10.1007/s12035-016-9725-5
  20. with Glioma in a Chinese Population vol.19, pp.1, 2015, https://doi.org/10.1089/gtmb.2014.0228