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印度东北部民族人群鼻咽癌中代谢I期(细胞色素P450酶系)和II期(谷胱甘肽S-转移酶)基因多态性及其与环境因素的相互作用

Metabolic Phase I (CYPs) and Phase II (GSTs) Gene Polymorphisms and Their Interaction with Environmental Factors in Nasopharyngeal Cancer from the Ethnic Population of Northeast India.

作者信息

Singh Seram Anil, Ghosh Sankar Kumar

机构信息

Molecular Medicine Laboratory, Department of Biotechnology, Assam University, Silchar, Assam, Pin-788011, India.

Department of Applied Biology, School of Biological Sciences, University of Science and Technology, Ri-Bhoi, Meghalaya, Pin-793101, India.

出版信息

Pathol Oncol Res. 2019 Jan;25(1):33-44. doi: 10.1007/s12253-017-0309-0. Epub 2017 Sep 26.

Abstract

Multiple genetic and environmental factors and their interaction are believed to contribute in the pathogenesis of Nasopharyngeal Cancer (NPC). We investigate the role of Metabolic Phase I (CYPs) and Phase II (GSTs) gene polymorphisms, gene-gene and gene-environmental interaction in modulating the susceptibility to NPC in Northeast India. To determine the association of metabolic gene polymorphisms and environmental habits, 123 cases and 189 controls blood/swab samples were used for PCR and confirmed by Sanger sequencing. Analysis for GSTM1 and GSTT1 gene polymorphism was done by multiplex PCR. The T3801C in the 3'- flanking region of CYP1A1 gene was detected by PCR-RFLP method. The Logistic regression analysis was used to estimate odds ratios (OR) and 95% confidence intervals (95% CI). The GSTM1 null genotype alone (OR = 2.76) was significantly associated with NPC risk (P < 0.0001). The combinations of GSTM1 null and GSTT1 null genotypes also higher, 3.77 fold (P < 0.0001), risk of NPC, while GSTM1 null genotype along with CYP1A1 T3801C TC + CC genotype had 3.22 (P = 0.001) fold risk. The most remarkable risk was seen among individual carrying GSTM1 null, GSTT1 null genotypes and CYP1A1 T3801C TC + CC genotypes (OR = 5.71, P = 0.001). Further; analyses demonstrate an enhanced risk of NPC in smoked meat (OR = 5.56, P < 0.0001) and fermented fish consumers (OR = 5.73, P < 0.0001) carrying GSTM1 null genotype. An elevated risk of NPC was noted in smokers (OR = 12.67, P < 0.0001) and chewers (OR = 5.68, P < 0.0001) with GSTM1 null genotype. However, smokers had the highest risk of NPC among individuals carrying GSTT1 null genotype (OR = 4.46, P = 0.001) or CYP1A1 T3801C TC + CC genotype (OR = 7.13, P < 0.0001). The association of null genotypes and mutations of metabolic neutralizing genes along with the environmental habits (tobacco smokers and chewers, smoke meat, fermented fishes) can be used as a possible biomarker for early detection and preventive measure of NPC.

摘要

多种遗传和环境因素及其相互作用被认为与鼻咽癌(NPC)的发病机制有关。我们研究了代谢I期(CYPs)和II期(GSTs)基因多态性、基因-基因以及基因-环境相互作用在调节印度东北部人群对NPC易感性中的作用。为了确定代谢基因多态性与环境习惯之间的关联,我们使用了123例病例和189例对照的血液/拭子样本进行PCR,并通过桑格测序进行确认。通过多重PCR对GSTM1和GSTT1基因多态性进行分析。采用PCR-RFLP方法检测CYP1A1基因3'侧翼区域的T3801C。使用逻辑回归分析来估计比值比(OR)和95%置信区间(95%CI)。单独的GSTM1无效基因型(OR = 2.76)与NPC风险显著相关(P < 0.0001)。GSTM1无效和GSTT1无效基因型的组合也具有更高的,3.77倍(P < 0.0001),NPC风险,而GSTM1无效基因型与CYP1A1 T3801C TC + CC基因型具有3.22倍(P = 0.001)的风险。在携带GSTM1无效、GSTT1无效基因型和CYP1A1 T3801C TC + CC基因型的个体中观察到最显著的风险(OR = 5.71,P = 0.001)。此外;分析表明,携带GSTM1无效基因型的烟熏肉消费者(OR = 5.56,P < 0.0001)和发酵鱼消费者(OR = 5.73,P < 0.0001)患NPC的风险增加。在携带GSTM1无效基因型的吸烟者(OR = 12.67,P < 0.0001)和咀嚼者(OR = 5.68,P < 0.0001)中,NPC风险升高。然而,在携带GSTT1无效基因型(OR = 4.46,P = 0.001)或CYP1A1 T3801C TC + CC基因型(OR = 7.13,P < 0.0001)的个体中,吸烟者患NPC的风险最高。代谢中和基因的无效基因型和突变与环境习惯(吸烟者和咀嚼者、烟熏肉、发酵鱼)之间的关联可作为NPC早期检测和预防措施的可能生物标志物。

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