Department of Medical Laboratory Science and Biotechnology, Central Taiwan University of Science and Technology, Taichung, Taiwan, R.O.C.
Graduate Institute of Biomedical Sciences, China Medical University, Taichung, Taiwan, R.O.C.
Cancer Genomics Proteomics. 2021 May-Jun;18(3 Suppl):441-449. doi: 10.21873/cgp.20270.
BACKGROUND/AIM: Xeroderma pigmentosum complementation group C (XPC) is reported to play important roles in DNA integrity and genomic instability, however, the contribution of XPC to oral carcinogenesis is largely uncertain. Therefore, we aimed at examining the contribution of XPC genotypes to oral cancer.
The genotypes of XPC rs2228001 and rs2228000 were examined among 958 oral cancer patients and 958 control subjects by polymerase chain reaction-restriction fragment length polymorphism methodology and corresponding DNA repair capacity was checked.
First, the percentages of XPC rs2228001 AC and CC were higher among oral cancer patients than controls. Second, no significant association was observed regarding XPC rs2228000. Third, there was a synergistic influence of smoking and betel quid chewing behaviors and XPC rs2228001 genotype on oral cancer risk. Last, functional experiments showed DNA repair capacity was lower for AC/CC carriers than AA carriers.
XPC rs2228001 C allele, which was associated with decreased DNA repair capacity, may interact with smoking and betel quid chewing behaviors on oral cancer risk.
背景/目的:着色性干皮病互补组 C(XPC)据报道在 DNA 完整性和基因组不稳定性中发挥重要作用,然而,XPC 对口腔癌发生的贡献在很大程度上仍不确定。因此,我们旨在研究 XPC 基因型对口腔癌的贡献。
通过聚合酶链反应-限制性片段长度多态性方法检测 958 例口腔癌患者和 958 例对照者 XPC rs2228001 和 rs2228000 的基因型,并检查相应的 DNA 修复能力。
首先,XPC rs2228001 AC 和 CC 在口腔癌患者中的比例高于对照组。其次,XPC rs2228000 与口腔癌无明显相关性。第三,吸烟和咀嚼槟榔行为与 XPC rs2228001 基因型对口腔癌风险有协同影响。最后,功能实验表明 AC/CC 携带者的 DNA 修复能力低于 AA 携带者。
与 DNA 修复能力降低相关的 XPC rs2228001 C 等位基因可能与吸烟和咀嚼槟榔行为相互作用,增加口腔癌的风险。