Developmental Toxicology Division, Indian Institute of Toxicology Research (Formerly: Industrial Toxicology Research Centre), Council CSIR, P.O. Box 80, Mahatma Gandhi Marg, Lucknow 226 001, India.
Mutat Res. 2010 Feb 3;684(1-2):49-55. doi: 10.1016/j.mrfmmm.2009.11.010. Epub 2009 Nov 30.
The present case-control study attempted to investigate the association of poor metabolizer (PM) genotypes of cytochrome P450 2D6 (CYP2D64 and CYP2D610) with squamous cell carcinoma of head and neck (HNSCC) and treatment response in patients receiving chemotherapy or combination of chemo- and radiotherapy. Cases with the PM genotypes of CYP2D6 displayed a significantly increased risk for HNSCC as compared to wild type genotypes. The risk was found to further increase in cases (up to 4.8) carrying combination of PM genotypes of CYP2D6, CYP2C9 (CYP2C92) or CYP2C19 (CYP2C192), suggesting that synergism amongst the PM genotypes of drug metabolizing CYPs leads to impairment in the detoxification of the tobacco carcinogens. A small increase in the risk in tobacco (chewers or smokers) or alcohol users in cases with CYP2D64 allele while no change or even a small decrease in risk in cases with CYP2D610 allele when compared to non-tobacco or alcohol users have suggested that CYP2D6 genotypes alone do not appear to interact significantly with environmental risk factors in modifying the susceptibility to HNSCC. Furthermore, most of the cases carrying PM genotypes of CYP2D6 did not respond to the treatment. Moreover, higher prevalence of non-responders among cases carrying combination of CYP2D64 or CYP2D64, CYP2C92 and CYP2C192 have demonstrated that interaction of PM genotypes may not only significantly modify the susceptibility to HNSCC but also the treatment response.
本病例对照研究试图探讨细胞色素 P450 2D6(CYP2D64 和 CYP2D610)的弱代谢者(PM)基因型与头颈部鳞状细胞癌(HNSCC)以及接受化疗或化疗联合放疗的患者治疗反应之间的关联。与野生型基因型相比,携带 CYP2D6 PM 基因型的病例发生 HNSCC 的风险显著增加。研究发现,携带 CYP2D6、CYP2C9(CYP2C92)或 CYP2C19(CYP2C192)PM 基因型组合的病例风险进一步增加(高达 4.8),表明药物代谢 CYP 的 PM 基因型之间存在协同作用,导致烟草致癌物质的解毒作用受损。与非烟草或非酒精使用者相比,携带 CYP2D64 等位基因的病例中烟草(咀嚼者或吸烟者)或酒精使用者的风险略有增加,而携带 CYP2D610 等位基因的病例中风险没有变化甚至略有下降,这表明 CYP2D6 基因型单独似乎不会与环境危险因素显着相互作用,从而改变对 HNSCC 的易感性。此外,大多数携带 CYP2D6 PM 基因型的病例对治疗没有反应。此外,携带 CYP2D64 或 CYP2D64、CYP2C92 和 CYP2C192 组合的病例中无反应者的比例较高,表明 PM 基因型的相互作用不仅可能显着改变 HNSCC 的易感性,还可能改变治疗反应。