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Active mitochondrial respiration in cancer: a target for the drug.
- Source :
-
Molecular and cellular biochemistry [Mol Cell Biochem] 2022 Feb; Vol. 477 (2), pp. 345-361. Date of Electronic Publication: 2021 Oct 30. - Publication Year :
- 2022
-
Abstract
- The relative contribution of mitochondrial respiration and subsequent energy production in malignant cells has remained controversial to date. Enhanced aerobic glycolysis and impaired mitochondrial respiration have gained more attention in the metabolic study of cancer. In contrast to the popular concept, mitochondria of cancer cells oxidize a diverse array of metabolic fuels to generate a majority of the cellular energy by respiration. Several mitochondrial respiratory chain (MRC) subunits' expressions are critical for the growth, metastasis, and cancer cell invasion. Also, the assembly factors, which regulate the integration of individual MRC complexes into native super-complexes, are upregulated in cancer. Moreover, a series of anti-cancer drugs function by inhibiting respiration and ATP production. In this review, we have specified the roles of mitochondrial fuels, MRC subunits, and super-complex assembly factors that promote active respiration across different cancer types and discussed the potential roles of MRC inhibitor drugs in controlling cancer.<br /> (© 2021. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)
- Subjects :
- Electron Transport Complex I genetics
Electron Transport Complex I metabolism
Humans
Mitochondria genetics
Neoplasm Proteins genetics
Neoplasm Proteins metabolism
Neoplasms genetics
Neoplasms metabolism
Oxidation-Reduction
Oxygen Consumption genetics
Antineoplastic Agents therapeutic use
Drug Delivery Systems
Mitochondria metabolism
Neoplasms drug therapy
Oxygen Consumption drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1573-4919
- Volume :
- 477
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Molecular and cellular biochemistry
- Publication Type :
- Academic Journal
- Accession number :
- 34716860
- Full Text :
- https://doi.org/10.1007/s11010-021-04281-4