» Articles » PMID: 30429230

Impact of Polymorphisms in DNA Repair Genes XPD, HOGG1 and XRCC4 on Colorectal Cancer Risk in a Chinese Han Population

Overview
Journal Biosci Rep
Specialty Cell Biology
Date 2018 Nov 16
PMID 30429230
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

Background: This research aimed to study the associations between XPD (G751A, rs13181), hOGG1 (C326G, rs1052133) and XRCC4 (G1394T, rs6869366) gene polymorphisms and the risk of colorectal cancer (CRC) in a Chinese Han population.

Method: A total of 225 Chinese Han patients with CRC were selected as the study group, and 200 healthy subjects were recruited as the control group. The polymorphisms of XPD G751A, hOGG1 C326G and XRCC4 G1394T loci were detected by the RFLP-PCR technique in the peripheral blood of all subjects.

Results: Compared with individuals carrying the XPD751 GG allele, the A allele carriers (GA/AA) had a significantly increased risk of CRC (adjusted OR = 2.109, 95%CI = 1.352-3.287, =0.003). Similarly, the G allele (CG/GG) of hOGG1 C326G locus conferred increased susceptibility to CRC (adjusted OR = 2.654, 95%CI = 1.915-3.685, <0.001). In addition, the T allele carriers (GT/TT) of the XRCC4 G1394T locus have an increased risk of developing CRC (adjusted OR = 4.512, 95%CI = 2.785-7.402, 0.001). The risk of CRC was significantly increased in individuals with both the XPD locus A allele and the hOGG1 locus G allele (adjusted OR = 1.543, 95%CI = 1.302-2.542, =0.002). Furthermore, individuals with both the hOGG1 locus G allele and the XRCC4 locus T allele were predisposed to CRC development (adjusted OR = 3.854, 95%CI = 1.924-7.123, <0.001). The risks of CRC in XPD gene A allele carriers (GA/AA) (adjusted OR = 1.570, 95%CI = 1.201-1.976, =0.001), hOGG1 gene G allele carriers (CG/GG) (adjusted OR = 3.031, 95%CI = 2.184-4.225, <0.001) and XRCC4 gene T allele carriers (GT/TT) (adjusted OR = 2.793, 95%CI = 2.235-3.222, <0.001) were significantly higher in patients who smoked ≥16 packs/year.

Conclusion: Our results suggest that XPD G751A, hOGG1 C326G and XRCC4 G1394T gene polymorphisms might play an important role in colorectal carcinogenesis and increase the risk of developing CRC in the Chinese Han population. The interaction between smoking and these gene polymorphisms would increase the risk of CRC.

Citing Articles

Nucleotide excision repair gene polymorphisms and hepatoblastoma susceptibility in Eastern Chinese children: A five-center case-control study.

Yin H, Wang X, Zhang S, He S, Zhang W, Lu H Chin J Cancer Res. 2024; 36(3):298-305.

PMID: 38988482 PMC: 11230887. DOI: 10.21147/j.issn.1000-9604.2024.03.06.


The Contribution of DNA Ligase 4 Polymorphisms to Colorectal Cancer.

Deng Y, Ke T, Yueh T, Chin Y, Wang Y, Hung Y In Vivo. 2023; 38(1):127-133.

PMID: 38148049 PMC: 10756467. DOI: 10.21873/invivo.13419.


Polymorphisms of nucleotide excision repair genes associated with colorectal cancer risk: Meta-analysis and trial sequential analysis.

Yi C, Li T, Shen Y, Wang P, Dai L, Shi J Front Genet. 2022; 13:1009938.

PMID: 36386844 PMC: 9659581. DOI: 10.3389/fgene.2022.1009938.


The Association of Single-Nucleotide Polymorphism rs13181 in ERCC2 with Risk and Prognosis of Nasopharyngeal Carcinoma in an Endemic Chinese Population.

Wei Z, Yao M, Ning S, Wu Y, Zhou X, Zhong C Pharmgenomics Pers Med. 2021; 14:359-367.

PMID: 33762840 PMC: 7982703. DOI: 10.2147/PGPM.S296215.


XRCC4 rs28360071 intronic variant is associated with increased risk for infant acute lymphoblastic leukemia with KMT2A rearrangements.

Louzada-Neto O, Lopes B, Brisson G, Andrade F, Cezar I, Santos-Reboucas C Genet Mol Biol. 2020; 43(4):e20200160.

PMID: 33270074 PMC: 7734917. DOI: 10.1590/1678-4685-GMB-2020-0160.

References
1.
Armaghany T, Wilson J, Chu Q, Mills G . Genetic alterations in colorectal cancer. Gastrointest Cancer Res. 2012; 5(1):19-27. PMC: 3348713. View

2.
Ataian Y, Krebs J . Five repair pathways in one context: chromatin modification during DNA repair. Biochem Cell Biol. 2006; 84(4):490-504. DOI: 10.1139/o06-075. View

3.
Slyskova J, Naccarati A, Pardini B, Polakova V, Vodickova L, Smerhovsky Z . Differences in nucleotide excision repair capacity between newly diagnosed colorectal cancer patients and healthy controls. Mutagenesis. 2012; 27(2):225-32. DOI: 10.1093/mutage/ger088. View

4.
Sliwinski T, Krupa R, Wisniewska-Jarosinska M, Pawlowska E, Lech J, Chojnacki J . Common polymorphisms in the XPD and hOGG1 genes are not associated with the risk of colorectal cancer in a Polish population. Tohoku J Exp Med. 2009; 218(3):185-91. DOI: 10.1620/tjem.218.185. View

5.
Siegel R, Miller K, Fedewa S, Ahnen D, Meester R, Barzi A . Colorectal cancer statistics, 2017. CA Cancer J Clin. 2017; 67(3):177-193. DOI: 10.3322/caac.21395. View