Hypoxia-regulated microRNA-210 modulates mitochondrial function and decreases ISCU and COX10 expression

Oncogene

Volumn 29, Issue 30, 2010, Pages 4362-4368

  Chen, Z ^a   Li, Y ^a   Zhang, H ^a   Huang, P ^a   Luthra, R ^a  

^a UNIVERSITY OF TEXAS MD ANDERSON CANCER CENTER   (United States)

Author keywords

COX10; hypoxia; ISCU; miR 210; mitochondria; ROS

Indexed keywords

CYTOCHROME C OXIDASE; HYPOXIA INDUCIBLE FACTOR 1ALPHA; IRON SULFUR CLUSTER SCAFFOLD HOMOLOG; IRON SULFUR PROTEIN; MESSENGER RNA; MICRORNA; MICRORNA 210; REACTIVE OXYGEN METABOLITE; UNCLASSIFIED DRUG;

ARTICLE; CANCER CELL; CANCER CELL CULTURE; CELL PROLIFERATION; CITRIC ACID CYCLE; COLON CANCER; CONTROLLED STUDY; CYTOTOXICITY; ELECTRON TRANSPORT; HOMEOSTASIS; HUMAN; HUMAN TISSUE; HYPOXIA; IRON METABOLISM; MITOCHONDRIAL MEMBRANE POTENTIAL; MITOCHONDRIAL RESPIRATION; MITOCHONDRION; OXIDATIVE PHOSPHORYLATION; PRIORITY JOURNAL; REAL TIME POLYMERASE CHAIN REACTION; WESTERN BLOTTING;

3' UNTRANSLATED REGIONS; ALKYL AND ARYL TRANSFERASES; CELL HYPOXIA; CELL LINE, TUMOR; CELL PROLIFERATION; GENE EXPRESSION REGULATION, NEOPLASTIC; GLYCOLYSIS; HUMANS; IRON-SULFUR PROTEINS; MEMBRANE POTENTIALS; MEMBRANE PROTEINS; MICRORNAS; MITOCHONDRIA; OXYGEN CONSUMPTION; REACTIVE OXYGEN SPECIES;

EID: 77955170881     PISSN: 09509232     EISSN: 14765594     Source Type: Journal    
DOI: 10.1038/onc.2010.193     Document Type: Article

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