Alteration of the bioenergetic phenotype of mitochondria is a hallmark of breast, gastric, lung and oesophageal cancer

被引:166
作者
Isidoro, A
Martínez, M
Fernández, PL
Ortega, AD
Santamaría, G
Chamorro, M
Reed, JC
Cuezva, JM [1 ]
机构
[1] Univ Autonoma Madrid, CSIC, CBMSO, Dept Mol Biol, Madrid 28049, Spain
[2] Hosp Clin Barcelona, IDIBAPS, Dept Anat Patol, Barcelona, Spain
[3] Burnham Inst, La Jolla, CA 92037 USA
关键词
cancer; glycolysis; H+-ATP synthase; mitochondria;
D O I
10.1042/BJ20031541
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
Recent findings indicate that the expression of the beta-catalytic subunit of the mitochondrial H+-ATP synthase (beta-F-1-ATPase) is depressed in liver, kidney and colon carcinomas, providing further a bioenergetic signature of cancer that is associated with patient survival. in the present study, we performed an analysis of mitochondrial and Glycolytic protein markers in breast, gastric and prostate adenocarcinomas. and in squamous oesophageal and lung carcinomas. The expression of mitochondrial and glycolytic markers varied significantly in these carcinomas, when compared with paired normal tissues, with the exception of prostate cancer. Overall, the relative expression of beta-F-1-ATPase was significantly reduced in breast and gastric adenocarcinomas, as well as in squamous oesophageal and lung carcinomas, strongly suggesting that alteration of the bioenergetic function of mitochondria is a hallmark of these types of cancer.
引用
收藏
页码:17 / 20
页数:4
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