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

• Published in: Seminars in cancer biology 2017-12, Vol.47, p.43-49
• Main Authors: Deng, Pan, Haynes, Cole M
• Format: Article
• Language: English
• Subjects: Activating Transcription Factors - genetics; Activating Transcription Factors - metabolism; Animals; ATF5; Cancer; Gene Expression Regulation, Neoplastic; Hematology, Oncology and Palliative Medicine; Humans; Mitochondria; Mitochondria - metabolism; Neoplasms - etiology; Neoplasms - metabolism; Signal Transduction; Stress, Physiological; Unfolded Protein Response; UPRmt
• ISSN: 1044-579X; 1096-3650
• DOI: 10.1016/j.semcancer.2017.05.002

Abstract 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 mitochondrial genome mutagenesis, we examine potential roles for a mitochondrial-protective transcriptional response known as the mitochondrial unfolded protein response (UPRmt ) in cancer cell biology.