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细胞色素 P4502A6 多态性降低头颈部癌症风险并影响治疗效果。

Polymorphism in cytochrome P4502A6 reduces the risk to head and neck cancer and modifies the treatment outcome.

机构信息

System Toxicology and Health Risk Assessment Group, CSIR-Indian Institute of Toxicology Research, Lucknow, India.

Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, India.

出版信息

Environ Mol Mutagen. 2021 Nov;62(9):502-511. doi: 10.1002/em.22466. Epub 2021 Oct 26.

Abstract

The present case-control study consisting of 1300 cases of head and neck squamous cell carcinoma (HNSCC) and the equal number of controls aimed to investigate the association of functionally important polymorphisms in cytochrome P4502A6 (CYP2A61B, CYP2A64C, CYP2A69-rs28399433) with HNSCC and the treatment response in cases receiving a combination of chemotherapy/radiotherapy (CT/RT). A significant decrease in risk to HNSCC was observed in the cases with deletion (CYP2A64B and CYP2A64C) or reduced activity genotypes (CYP2A69) of CYP2A6. This risk to HNSCC was further reduced significantly in tobacco users among the cases when compared to nontobacco users among the cases. The risk was also reduced to a slightly greater extent in alcohol users among the cases when compared to nonalcohol users among the cases. In contrast with decreased risk to HNSCC, almost half of the cases with variant genotypes of CYP2A6 (CYP2A6*1A/*4C+*1B/*4C+*4C/*4C and *9/*9) did not respond to the treatment. Likewise, the survival rate in cases receiving the treatment, after 55 months of follow-up was significantly lower in cases with deletion (6.3%) or reduced activity (11.9%) allele than in the cases with common alleles (41%). The present study has shown that CYP2A6 polymorphism significantly reduces the risk to HNSCC. Our data further suggested that CYP2A6 polymorphism may worsen the treatment outcome in the cases receiving CT/RT.

摘要

本病例对照研究纳入了 1300 例头颈部鳞状细胞癌(HNSCC)病例和相同数量的对照,旨在研究细胞色素 P4502A6(CYP2A61B、CYP2A64C、CYP2A69-rs28399433)中功能重要的多态性与 HNSCC 的相关性,以及接受化疗/放疗(CT/RT)联合治疗的病例的治疗反应。CYP2A6 缺失(CYP2A64B 和 CYP2A64C)或活性降低(CYP2A69)基因型的病例发生 HNSCC 的风险显著降低。与病例中的非吸烟组相比,吸烟病例中这种 HNSCC 的风险进一步显著降低。与病例中的非饮酒组相比,饮酒病例中这种风险也略有更大程度降低。与 HNSCC 风险降低相反,几乎一半的 CYP2A6 变异基因型(CYP2A6*1A/*4C+*1B/*4C+*4C/*4C 和 *9/*9)的病例对治疗没有反应。同样,经过 55 个月的随访,接受治疗的病例中,缺失(6.3%)或活性降低(11.9%)等位基因的病例的生存率明显低于常见等位基因(41%)的病例。本研究表明 CYP2A6 多态性显著降低了 HNSCC 的风险。我们的数据进一步表明,CYP2A6 多态性可能会使接受 CT/RT 的病例的治疗结果恶化。

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