Shankaran Zioni Sangeetha, Walter Charles Emmanuel Jebaraj, Prakash Nandini, Ramachandiran Kotteeswaran, C George Priya Doss, Johnson Thanka
Department of Biotechnology, Sri Ramachandra Institute of Higher Education & Research (Deemed to be University), Chennai, India.
Department of Integrative Biology, School of Bio Sciences and Technology, Vellore Institute of Technology, Vellore, India.
Heliyon. 2020 Mar 12;6(3):e03565. doi: 10.1016/j.heliyon.2020.e03565. eCollection 2020 Mar.
Gastrointestinal (GI) cancers are known to have a high incidence worldwide and require an early diagnosis to successfully treat them, providing higher survival rates and better quality of life for the patients. MicroRNA-27a is a well-known oncogene that plays a significant role in various GI cancers. It is known to upregulate the expression of numerous oncogenes leading to cancer progression. The miR-27a harbors two polymorphisms rs895819 and rs11671784 which alter the disease susceptibility by interfering with the maturation and expression of miR-27a. In the current study, we aimed to investigate the role played by these polymorphisms in cancers of the GI tract. We conducted a case-control study with 210 GI cancer cases and 210 cancer-free controls to analyze the effect of these polymorphisms. The rs895819 polymorphism was genotyped using PCR-RFLP, and rs11671784 was genotyped on a MassARRAY platform. The association analysis failed to bring out any significant association of the polymorphisms with GI cancer risk. However, genotype-phenotype interaction analysis revealed that the rs895819 was found to increase the risk GI cancers along with the presence of risk factors such as socioeconomic status, diabetes mellitus, hypertension, alcohol consumption, and tobacco chewing.
已知胃肠道(GI)癌症在全球范围内发病率很高,需要早期诊断以成功治疗,从而为患者提供更高的生存率和更好的生活质量。MicroRNA-27a是一种著名的致癌基因,在各种胃肠道癌症中起重要作用。已知它会上调许多致癌基因的表达,导致癌症进展。miR-27a存在两种多态性rs895819和rs11671784,它们通过干扰miR-27a的成熟和表达来改变疾病易感性。在本研究中,我们旨在调查这些多态性在胃肠道癌症中的作用。我们进行了一项病例对照研究,纳入210例胃肠道癌症病例和210例无癌对照,以分析这些多态性的影响。rs895819多态性通过PCR-RFLP进行基因分型,rs11671784在MassARRAY平台上进行基因分型。关联分析未能发现这些多态性与胃肠道癌症风险有任何显著关联。然而,基因型-表型相互作用分析显示,rs895819与社会经济地位、糖尿病、高血压、饮酒和嚼烟等危险因素同时存在时,会增加患胃肠道癌症的风险。