Targeting Glucose Metabolism in Patients With Cancer

被引:126
作者
Elf, Shannon E. [1 ]
Chen, Jing [1 ]
机构
[1] Emory Univ, Sch Med, Dept Hematol & Med Oncol, Winship Canc Inst, Atlanta, GA 30322 USA
关键词
the Warburg effect; cancer metabolism; metabolic enzymes; small-molecule inhibitors; anticancer targets; PYRUVATE-KINASE M2; PHOSPHOGLYCERATE MUTASE 1; TUMOR-GROWTH; TYROSINE PHOSPHORYLATION; CELL METABOLISM; LACTATE-DEHYDROGENASE; DICHLOROACETATE DCA; IDH2; MUTATIONS; L-ASPARAGINASE; DIFFERENTIATION;
D O I
10.1002/cncr.28501
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Nearly a century ago, Otto Warburg made the astute observation that the metabolic properties of cancer cells differ markedly from those of normal cells. Several decades passed before the concept of exploiting cancer cell metabolism came into clinical practice with the advent of chemotherapy, the underlying principle of which is to target rapidly dividing cells by interfering with critical processes that are all, on some level, driven by cell metabolism. Although chemotherapy can be quite effective, success rates are highly variable and the adverse effects associated with treatment often outweigh the benefits due to the fact that chemotherapy is indiscriminately cytotoxic against all rapidly dividing cells, cancerous or healthy. During the past several years, a more intricate understanding of cancer cell metabolism has permitted the development of targeted therapies that aim to specifically target cancer cells and spare healthy tissue by exploiting the altered metabolism of cancer cells. The identification of new metabolic targets and the subsequent development of small-molecule inhibitors of metabolic enzymes have demonstrated the utility and promise of targeting cancer cell metabolism as an anticancer strategy. This review summarizes recent advances in the identification and characterization of several metabolic enzymes as emerging anticancer targets. Cancer 2014;120:774-780. (c) 2013 American Cancer Society. Nearly a century ago, Otto Warburg made the astute observation that the metabolic properties of cancer cells differ markedly from those of normal cells. Tools are now available to identify new metabolic targets and develop novel anticancer strategies by targeting cancer cell metabolism.
引用
收藏
页码:774 / 780
页数:7
相关论文
共 50 条
[1]
Pyruvate kinase M2 activators promote tetramer formation and suppress tumorigenesis [J].
Anastasiou, Dimitrios ;
Yu, Yimin ;
Israelsen, William J. ;
Jiang, Jian-Kang ;
Boxer, Matthew B. ;
Hong, Bum Soo ;
Tempel, Wolfram ;
Dimov, Svetoslav ;
Shen, Min ;
Jha, Abhishek ;
Yang, Hua ;
Mattaini, Katherine R. ;
Metallo, Christian M. ;
Fiske, Brian P. ;
Courtney, Kevin D. ;
Malstrom, Scott ;
Khan, Tahsin M. ;
Kung, Charles ;
Skoumbourdis, Amanda P. ;
Veith, Henrike ;
Southall, Noel ;
Walsh, Martin J. ;
Brimacombe, Kyle R. ;
Leister, William ;
Lunt, Sophia Y. ;
Johnson, Zachary R. ;
Yen, Katharine E. ;
Kunii, Kaiko ;
Davidson, Shawn M. ;
Christofk, Heather R. ;
Austin, Christopher P. ;
Inglese, James ;
Harris, Marian H. ;
Asara, John M. ;
Stephanopoulos, Gregory ;
Salituro, Francesco G. ;
Jin, Shengfang ;
Dang, Lenny ;
Auld, Douglas S. ;
Park, Hee-Won ;
Cantley, Lewis C. ;
Thomas, Craig J. ;
Heiden, Matthew G. Vander .
NATURE CHEMICAL BIOLOGY, 2012, 8 (10) :839-847
[2]
Targeting Cancer Cell Metabolism: The Combination of Metformin and 2-Deoxyglucose Induces p53-Dependent Apoptosis in Prostate Cancer Cells [J].
Ben Sahra, Issam ;
Laurent, Kathiane ;
Giuliano, Sandy ;
Larbret, Frederic ;
Ponzio, Gilles ;
Gounon, Pierre ;
Le Marchand-Brustel, Yannick ;
Giorgetti-Peraldi, Sophie ;
Cormont, Mireille ;
Bertolotto, Corine ;
Deckert, Marcel ;
Auberger, Patrick ;
Tanti, Jean-Francois ;
Bost, Frederic .
CANCER RESEARCH, 2010, 70 (06) :2465-2475
[3]
A mitochondria-K+ channel axis is suppressed in cancer and its normalization promotes apoptosis and inhibits cancer growth [J].
Bonnet, Sebastien ;
Archer, Stephen L. ;
Allalunis-Turner, Joan ;
Haromy, Alois ;
Beaulieu, Christian ;
Thompson, Richard ;
Lee, Christopher T. ;
Lopaschuk, Gary D. ;
Puttagunta, Lakshmi ;
Bonnet, Sandra ;
Harry, Gwyneth ;
Hashimoto, Kyoko ;
Porter, Christopher J. ;
Andrade, Miguel A. ;
Thebaud, Bernard ;
Michelakis, Evangelos D. .
CANCER CELL, 2007, 11 (01) :37-51
[4]
BROOME JD, 1981, CANCER TREAT REP, V65, P111
[5]
Regulation of cancer cell metabolism [J].
Cairns, Rob A. ;
Harris, Isaac S. ;
Mak, Tak W. .
NATURE REVIEWS CANCER, 2011, 11 (02) :85-95
[6]
CAIRO MS, 1982, AM J PEDIAT HEMATOL, V4, P335
[7]
Dichloroacetate (DCA) sensitizes both wild-type and over expressing Bcl-2 prostate cancer cells in vitro to radiation [J].
Cao, Wengang ;
Yacoub, Saif ;
Shiverick, Kathleen T. ;
Namiki, Kazunori ;
Sakai, Yoshihisa ;
Porvasnik, Stacy ;
Urbanek, Cydney ;
Rosser, Charles J. .
PROSTATE, 2008, 68 (11) :1223-1231
[8]
The M2 splice isoform of pyruvate kinase is important for cancer metabolism and tumour growth [J].
Christofk, Heather R. ;
Vander Heiden, Matthew G. ;
Harris, Marian H. ;
Ramanathan, Arvind ;
Gerszten, Robert E. ;
Wei, Ru ;
Fleming, Mark D. ;
Schreiber, Stuart L. ;
Cantley, Lewis C. .
NATURE, 2008, 452 (7184) :230-U74
[9]
The regulation of energy generating metabolic pathways by p53 [J].
Corcoran, Chad A. ;
Huang, Ying ;
Sheikh, M. Saeed .
CANCER BIOLOGY & THERAPY, 2006, 5 (12) :1610-1613
[10]
Cancer-associated IDH1 mutations produce 2-hydroxyglutarate (vol 462, pg 739, 2010) [J].
Dang, Lenny ;
White, David W. ;
Gross, Stefan ;
Bennett, Bryson D. ;
Bittinger, Mark A. ;
Driggers, Edward M. ;
Fantin, Valeria R. ;
Jang, Hyun Gyung ;
Jin, Shengfang ;
Keenan, Marie C. ;
Marks, Kevin M. ;
Prins, Robert M. ;
Ward, Patrick S. ;
Yen, Katharine E. ;
Liau, Linda M. ;
Rabinowitz, Joshua D. ;
Cantley, Lewis C. ;
Thompson, Craig B. ;
Vander Heiden, Matthew G. ;
Su, Shinsan M. .
NATURE, 2010, 465 (7300) :966-966