Deciphering the Role of Mitochondrial Metabolic Reprogramming in the Progression of Clear Cell Renal Cell Carcinoma
- Authors
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Suresh Chandra Yadav
Kalinga University, Naya Raipur, Chhattisgarh, India -
Dilip Dwivedy
Kalinga University, Naya Raipur, Chhattisgarh, India
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- Keywords:
- Clear Cell Renal Cell Carcinoma (ccRCC), Mitochondrial Metabolic Reprogramming, Glycolysis, Oxidative Phosphorylation, Hypoxia-Inducible Factor (HIF-1α), Fatty Acid Oxidation, Therapeutic Targets
- Abstract
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The most prevalent and aggressive type of kidney cancer, which is known to be difficult to treat with standard therapies and has a poor prognosis, is clear cell renal cell carcinoma (ccRCC). It has been suggested that mitochondrial metabolic reprogramming is now a fundamental component of the development of ccRCC that affects energy generation, cell survival, and tumor aggressiveness. The aim of the study is to examine the importance of mitochondrial dysfunction in cRCC through imaging the metabolic changes that occur in the tumor microenvironment. A multi-omics method is used, which combines transcriptomic, metabolomic, and proteomic studies to reveal the metabolic changes that occur in the cells of ccRCC. Found that there were marked changes in some of the important metabolic pathways, such as increased glycolysis and fatty acid oxidation, as well as a significant decrease in the efficiency of oxidative phosphorylation. These were associated with metabolic alterations that correlated with a higher tumor cell survival and expansion in hypoxic conditions, which is typical of ccRCC. Moreover, several important regulators of metabolism, including HIF-1α, AMPK, and PGC-1α, were overexpressed in ccRCC cells and linked to the metabolic changes. Although HIF-1α, AMPK, and PGC-1α emerge as possible therapeutic targets, this paper does not involve any inhibition studies that would demonstrate the therapeutic value of these targets. The evidence presented here is purely correlational, involving only cell line and xenograft models. The given study contributes to the understanding of the metabolic weakness of the ccRCC and refers to the possibility of developing new treatment modalities that could influence the metabolism of mitochondria. Future studies ought to ultimately be on clinical validation of these findings and investigations on the development of mitochondrial-targeted therapies as monotherapies or as adjuncts to existing therapies in order to enhance patient outcomes in ccRCC.
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- 12-06-2026
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- Vol. 15 No. 1 (2026)
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