Mitochondrial dysfunction in cancer: Potential roles of ATF5 and the mitochondrial UPR

被引:82
作者
Deng, Pan [1 ,2 ]
Haynes, Cole M. [1 ,2 ]
机构
[1] Univ Massachusetts, Sch Med, Dept Mol Cell & Canc Biol, 364 Plantat St, Worcester, MA 01655 USA
[2] Weill Cornell Med Coll, BCMB Allied Program, 1300 York Ave, New York, NY 10065 USA
关键词
Mitochondria; UPRmt; ATF5; Cancer; UNFOLDED PROTEIN RESPONSE; TRANSCRIPTION FACTOR ATF5; INTEGRATED STRESS-RESPONSE; INDUCED GENE-EXPRESSION; DNA COPY NUMBER; OXIDATIVE STRESS; LON PROTEASE; COMPLEX-I; THERAPEUTIC STRATEGY; MESSENGER-RNA;
D O I
10.1016/j.semcancer.2017.05.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mitochondria form a cellular network of organelles, or cellular compartments, that efficiently couple nutrients to energy production in the form of ATP. As cancer cells rely heavily on glycolysis, historically mitochondria and the cellular pathways in place to maintain mitochondrial activities were thought to be more relevant to diseases observed in non-dividing cells such as muscles and neurons. However, more recently it has become clear that cancers rely heavily on mitochondrial activities including lipid, nucleotide and amino acid synthesis, suppression of mitochondria-mediated apoptosis as well as oxidative phosphorylation (OXPHOS) for growth and survival. Considering the variety of conditions and stresses that cancer cell mitochondria may incur such as hypoxia, reactive oxygen species and mitochondria' genome mutagenesis, we examine potential roles for a mitochondrial-protective transcriptional response known as the mitochondrial unfolded protein response (UPRmt) in cancer cell biology.
引用
收藏
页码:43 / 49
页数:7
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