The Mitochondrial Bioenergetic Capacity of Carcinomas

被引:37
|
作者
Formentini, Laura [1 ]
Martinez-Reyes, Inmaculada [1 ]
Cuezva, Jose M. [1 ]
机构
[1] Univ Autonoma Madrid, Ctr Biol Mol Severo Ochoa, Dept Biol Mol, CSIC,CIBERER ISCIII, E-28049 Madrid, Spain
关键词
mitochondria; glycolysis; cancer; H+-ATP synthase; Warburg phenotype; energetic metabolism; BETA-F1-ATPASE MESSENGER-RNA; H+-ATP SYNTHASE; CANCER-CELLS; C-MYC; OXIDATIVE-METABOLISM; PYRUVATE-KINASE; TUMOR-GROWTH; EXPRESSION; RESPIRATION; REPRESSION;
D O I
10.1002/iub.352
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Metabolic reprogramming of cancer cells is a phenotypic trait necessary to promote proliferation and survival. Despite past controversies, recent transcriptomic, proteomic, functional and structural studies of mitochondria of the cancer cell indicate that an impaired biogenesis and activity of the organelle is required for the development of some tumors. Cancer aggressiveness can be estimated by its bioenergetic signature, a protein ratio that correlates the expression of beta-F1-ATPase of oxidative phosphorylation relative to the glycolytic GAPDH. The bioenergetic signature also provides a gauge that informs of the metabolic activity of tumors and cancer cells as well as of the response to chemotherapy. The convergence of different epithelial tumors on the same bioenergetic signature supports that it provides an important tool and common target for cancer therapy. We stress that targeting the energetic metabolism of tumors affords a valuable strategy to combat the disease. (C) 2010 IUBMB IUBMB Life, 62(7): 554-560, 2010
引用
收藏
页码:554 / 560
页数:7
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