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
相关论文
共 141 条
[51]   Combinatorial drug design targeting multiple cancer signaling networks controlled by mitochondrial Hsp90 [J].
Kang, Byoung Heon ;
Plescia, Janet ;
Song, Ho Young ;
Meli, Massimiliano ;
Colombo, Giorgio ;
Beebe, Kristin ;
Scroggins, Bradley ;
Neckers, Len ;
Altieri, Dario C. .
JOURNAL OF CLINICAL INVESTIGATION, 2009, 119 (03) :454-464
[52]   A Synthetic Cell-Penetrating Dominant-Negative ATF5 Peptide Exerts Anticancer Activity against a Broad Spectrum of Treatment-Resistant Cancers [J].
Karpel-Massler, Georg ;
Horst, Basil A. ;
Shu, Chang ;
Chau, Lily ;
Tsujiuchi, Takashi ;
Bruce, Jeffrey N. ;
Canoll, Peter ;
Greene, Lloyd A. ;
Angelastro, James M. ;
Siegelin, Markus D. .
CLINICAL CANCER RESEARCH, 2016, 22 (18) :4698-4711
[53]   Mitochondria: from cell death executioners to regulators of cell differentiation [J].
Kasahara, Atsuko ;
Scorrano, Luca .
TRENDS IN CELL BIOLOGY, 2014, 24 (12) :761-770
[54]   FGF21 as a Stress Hormone: The Roles of FGF21 in Stress Adaptation and the Treatment of Metabolic Diseases [J].
Kim, Kook Hwan ;
Lee, Myung-Shik .
DIABETES & METABOLISM JOURNAL, 2014, 38 (04) :245-251
[55]   Autophagy deficiency leads to protection from obesity and insulin resistance by inducing Fgf21 as a mitokine [J].
Kim, Kook Hwan ;
Jeong, Yeon Taek ;
Oh, Hyunhee ;
Kim, Seong Hun ;
Cho, Jae Min ;
Kim, Yo-Na ;
Kim, Su Sung ;
Kim, Do Hoon ;
Hur, Kyu Yeon ;
Kim, Hyoung Kyu ;
Ko, TaeHee ;
Han, Jin ;
Kim, Hong Lim ;
Kim, Jin ;
Back, Sung Hoon ;
Komatsu, Masaaki ;
Chen, Hsiuchen ;
Chan, David C. ;
Konishi, Morichika ;
Itoh, Nobuyuki ;
Choi, Cheol Soo ;
Lee, Myung-Shik .
NATURE MEDICINE, 2013, 19 (01) :83-92
[56]   Neoplastic progression in melanoma and colon cancer is associated with increased expression and activity of the interferon-inducible protein kinase, PKR [J].
Kim, SH ;
Gunnery, S ;
Choe, JK ;
Mathews, MB .
ONCOGENE, 2002, 21 (57) :8741-8748
[57]   Human breast cancer cells contain elevated levels and activity of the protein kinase, PKR [J].
Kim, SH ;
Forman, AP ;
Mathews, MB ;
Gunnery, S .
ONCOGENE, 2000, 19 (27) :3086-3094
[58]   FGF21 is an endocrine signal of protein restriction [J].
Laeger, Thomas ;
Henagan, Tara M. ;
Albarado, Diana C. ;
Redman, Leanne M. ;
Bray, George A. ;
Noland, Robert C. ;
Muenzberg, Heike ;
Hutson, Susan M. ;
Gettys, Thomas W. ;
Schwartz, Michael W. ;
Morrison, Christopher D. .
JOURNAL OF CLINICAL INVESTIGATION, 2014, 124 (09) :3913-3922
[59]   Spectrum of somatic mitochondrial mutations in five cancers [J].
Larman, Tatianna C. ;
DePalma, Steven R. ;
Hadjipanayis, Angela G. ;
Protopopov, Alexei ;
Zhang, Jianhua ;
Gabriel, Stacey B. ;
Chin, Lynda ;
Seidman, Christine E. ;
Kucherlapati, Raju ;
Seidman, J. G. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2012, 109 (35) :14087-14091
[60]   Fumarate and Succinate Regulate Expression of Hypoxia-inducible Genes via TET Enzymes [J].
Laukka, Tuomas ;
Mariani, Christopher J. ;
Ihantola, Tuukka ;
Cao, John Z. ;
Hokkanen, Juho ;
Kaelin, William G., Jr. ;
Godley, Lucy A. ;
Koivunen, Peppi .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2016, 291 (08) :4256-4265