Mukherjee Debdutta, Devi Kangjam Rekha, Deka Manab, Malakar Mridul, Kaur Tanvir, Barua Debajit, Mahanta Jagadish, Narain Kanwar
Regional Medical Research Centre, N.E. Region (Indian Council of Medical Research), Post Box #105, Dibrugarh, 786 001, Assam, India.
Department of Biological Sciences, Gauhati University, Guwahati, Assam, India.
Tumour Biol. 2016 Aug;37(8):10821-6. doi: 10.1007/s13277-016-4982-5. Epub 2016 Feb 15.
Toll-like receptors (TLRs) are evolutionary conserved cell surface receptors of the innate immune system. Smoking has significant immunological effects which are mediated via TLRs on various receptor-mediated innate response pathways. Polymorphisms of TLR genes are associated with susceptibility toward various malignancies. The present study was undertaken to examine the association between TLR2 ∆22 and gastric cancer. In this study, we also investigated the interaction between TLR2 ∆22 and smoking. A total of 133 histologically confirmed gastric cancer cases and 266 age-sex-matched controls were selected for this study. TLR2 ∆22 genotypes were determined by allele-specific polymerase chain reaction (PCR). Binary conditional logistic regression analysis was used to find the association of TLR2 ∆22 with risk of gastric cancer. Logistic regression using hierarchically well-formulated models was used for interaction analysis between smoking and TLR2 ∆22. Persons having TLR2 ∆22 heterozygous genotype had two times increased risk of gastric cancer in multivariate logistic regression model. The interaction analysis using hierarchical logistic regression models between smoking and TLR2 ∆22 by calculating separate X (2) for interaction model and only main effect model, the difference of X (2) 57.68-47.70 = 9.98 and degrees of freedom (df) 5-3 = 2, revealed significant (α = 0.05, df = 2) omnibus interaction. Our present study revealed TLR2 ∆22 to be significantly and independently associated with gastric cancer risk in Mizoram, and there is also evidence of significant interaction between smoking and TLR2 ∆22 with risk of gastric cancer.
Toll样受体(TLRs)是先天性免疫系统中进化保守的细胞表面受体。吸烟具有显著的免疫效应,可通过TLRs介导多种受体介导的先天性反应途径。TLR基因的多态性与对各种恶性肿瘤的易感性相关。本研究旨在探讨TLR2 ∆22与胃癌之间的关联。在本研究中,我们还研究了TLR2 ∆22与吸烟之间的相互作用。本研究共选取了133例经组织学确诊的胃癌病例和266例年龄、性别匹配的对照。通过等位基因特异性聚合酶链反应(PCR)确定TLR2 ∆22基因型。采用二元条件逻辑回归分析来寻找TLR2 ∆22与胃癌风险的关联。使用层次结构良好的模型进行逻辑回归,以分析吸烟与TLR2 ∆22之间的相互作用。在多变量逻辑回归模型中,具有TLR2 ∆22杂合基因型的人患胃癌的风险增加了两倍。通过计算相互作用模型和仅主效应模型的单独X(2),使用层次逻辑回归模型对吸烟与TLR2 ∆22之间的相互作用进行分析,X(2)的差异为57.68 - 47.70 = 9.98,自由度(df)为5 - 3 = 2,显示出显著的(α = 0.05,df = 2)总体相互作用。我们目前的研究表明,在米佐拉姆邦,TLR2 ∆22与胃癌风险显著且独立相关,并且也有证据表明吸烟与TLR2 ∆22之间存在显著的相互作用,影响胃癌风险。