Department of Otolaryngology, Post Graduate Institute of Medical Education and Research, Chandigarh 160012, India.
Oral Dis. 2010 Oct;16(7):668-73. doi: 10.1111/j.1601-0825.2010.01676.x.
To investigate the role of aberrant hypermethylation of carcinogen metabolism pathway genes, CYP1A1, CYP2A13 and GSTM1 in head and neck cancer independently as well as its relation to tobacco and alcohol consumption and CYP1A1 and CYP2A13 polymorphisms in Indian population.
Seventy-three histologically confirmed head and neck cancer patients undergoing treatment in Postgraduate Institute of Medical Education and Research, Chandigarh, India were recruited. Non-cancerous tissues were obtained from 19 trauma subjects undergoing maxillofacial surgery. Methylation-specific PCR was performed to determine the methylation status of selected genes.
The aberrant hypermethylation of CYP1A1, CYP2A13 and GSTM1 genes was found in cancer tissues with frequency of about 39.7%, 27.4%, and 58.1%, respectively, and in normal healthy tissues with a frequency of about 10.5%, 15.8%, and 20.0%, respectively. Hypermethylation of CYP1A1 (P 0.027) and GSTM1 (P 0.010) showed significant association with head and neck cancer. We also observed significant interaction between smoking and methylation status of CYP1A1 (P 0.029) and CYP2A13 (P -0.034) in head and neck cancer. No association was observed between methylation status and alcohol consumption, clinical features and genetic polymorphisms of CYP1A1 and CYP2A13.
Hypermethylation of carcinogen metabolism pathway genes independently and in interaction with smoking is associated with increased risk of head and neck cancer.
研究致癌物质代谢途径基因 CYP1A1、CYP2A13 和 GSTM1 的异常高甲基化在印度人群中作为头颈部癌症的独立危险因素的作用,以及其与吸烟和饮酒的关系,以及 CYP1A1 和 CYP2A13 多态性。
在印度昌迪加尔的 PGIMER 研究所,我们招募了 73 名经组织学证实的头颈部癌症患者。从 19 名接受颌面外科手术的创伤患者中获得非癌组织。采用甲基化特异性 PCR 法确定所选基因的甲基化状态。
在癌症组织中,CYP1A1、CYP2A13 和 GSTM1 基因的异常高甲基化频率分别约为 39.7%、27.4%和 58.1%,而在正常健康组织中的频率分别约为 10.5%、15.8%和 20.0%。CYP1A1(P 0.027)和 GSTM1(P 0.010)的高甲基化与头颈部癌症显著相关。我们还观察到吸烟与 CYP1A1(P 0.029)和 CYP2A13(P -0.034)的甲基化状态之间存在显著的相互作用。CYP1A1 和 CYP2A13 的甲基化状态与饮酒、临床特征和遗传多态性之间无相关性。
致癌物质代谢途径基因的异常高甲基化独立于吸烟,并与头颈部癌症的风险增加有关。