Sneha Pramod - Department of Biomedical Sciences, Sri Ramachandra Institute of Higher Education and Research, Tamil Nadu, India
Suchitra Magesh - Department of Biomedical Sciences, Sri Ramachandra Institute of Higher Education and Research, Tamil Nadu, India
Venkatachalam Deepa Parvathi - Department of Biomedical Sciences, Sri Ramachandra Institute of Higher Education and Research, Tamil Nadu, India

Gastric carcinoma, in India, is the second most prevalent cause of cancer-related deaths since most patients are asymptomatic until the disease progresses to advanced stages. Hence, there is a need for non-invasive and specific biomarkers for early screening and diagnosis.Human mitochondrial DNA (mtDNA) has ۳۷ genes involved in oxidative phosphorylation pathway (OxPhos). There are several ۱۰۰ to ۱۰۰۰ mitochondria in a human cell and each mitochondrion has two to ۱۰ copies of mtDNA. There is a significant association between the mtDNA copy number and an increase in risk of various cancers.There is also a relation between the changes in the sequence of mtDNA in genes, such as MT-CYB, MT-ATP۶ and gastric cancer, according to which the tumor cells switch to aerobic glycolysis for ATP production even in the presence of oxygen due to Warburg effect. Multiple factors have an adverse effect on mitochondrial gene expression and impairs the OxPhos pathway due to lack of sophisticated DNA repair mechanism in mitochondria.Techniques, such as Next Generation Sequencing and Whole Genome Sequencing, are capable of early detection of copy number variants and mtDNA mutations in blood sample essential for better prognosis of gastric cancer.Through the course of this study, various reports of a correlation between mtDNA damage and gastric cancer were analyzed and it was found that the increasing evidence of the role of mtDNA and its copy number in cancer indicates its significance as a potential biomarker for gastric cancer.

Gastric Cancer, Mitochondrial DNA, Mutation