Saha Tania, Bhowmick Bismoy, Sengupta Debmalya, Banerjee Souradeep, Mitra Ritabrata, Sarkar Abhijit, Chaudhuri Tamohan, Bhattacharjee Gautam, Nath Somsubhra, Roychoudhury Susanta, Sengupta Mainak
Department of Genetics, University of Calcutta, Kolkata, West Bengal, India.
Department of Pulmonary medicine (Chest), IPGMER, Kolkata, West Bengal, India.
J Basic Clin Physiol Pharmacol. 2022 Mar 28;34(5):663-668. doi: 10.1515/jbcpp-2021-0352. eCollection 2023 Sep 1.
Mitochondrial dysfunction has long been associated with the pathogenesis of lung cancer (LC). Mitochondrial DNA (mtDNA) haplogroups have been reported to modify the risk of LC in a few different populations; however, no study has been done among the Indians. Here, we explore the relationship between mtDNA haplogroups and LC in a representative eastern Indian sample set.
Different combinations of six mtDNA SNPs, which define the major Asian mtDNA haplogroups M and N, and their sub-haplogroups D, G, M7, R, and F were genotyped via polymerase chain reaction (PCR) - restriction fragment length polymorphism (RFLP) - sequencing approach in 94 smoker LC patients and 100 healthy smoker controls from an eastern Indian cohort.
The distribution of 7 mtDNA haplogroups did not show any significant differences between patients and controls (p<0.05). We did not find sub-haplogroup M7 in our study population.
Our study is the first to indicate that the major Asian mtDNA haplogroups have no significant (p0.05) association with LC in East Indian population.
线粒体功能障碍长期以来一直与肺癌(LC)的发病机制相关。据报道,线粒体DNA(mtDNA)单倍群在一些不同人群中会改变患LC的风险;然而,在印度人群中尚未开展相关研究。在此,我们在一个具有代表性的东印度样本集中探究mtDNA单倍群与LC之间的关系。
通过聚合酶链反应(PCR)-限制性片段长度多态性(RFLP)-测序方法,对来自东印度队列的94例吸烟的LC患者和100例健康吸烟对照者进行基因分型,这些患者和对照者的六种mtDNA单核苷酸多态性(SNP)存在不同组合,这些SNP定义了主要的亚洲mtDNA单倍群M和N及其亚单倍群D、G、M7、R和F。
7种mtDNA单倍群的分布在患者和对照者之间未显示出任何显著差异(p<0.05)。我们在研究人群中未发现亚单倍群M7。
我们的研究首次表明,主要的亚洲mtDNA单倍群与东印度人群的LC无显著(p>0.05)关联。