Singh Seram Anil, Ghosh Sankar Kumar
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.
Pathol Oncol Res. 2019 Jan;25(1):33-44. doi: 10.1007/s12253-017-0309-0. Epub 2017 Sep 26.
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.
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。