Is cancer a disease of abnormal cellular metabolism? New angles on an old idea

被引:173
作者
DeBerardinis, Ralph J. [1 ,2 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Pediat, Dallas, TX 75390 USA
[2] Univ Texas SW Med Ctr Dallas, McDermott Ctr Human Growth & Dev, Dallas, TX 75390 USA
基金
美国国家卫生研究院;
关键词
cancer; metabolism; Warburg effect; glutamine; glucose;
D O I
10.1097/GIM.0b013e31818b0d9b
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
In the 1920s, Otto Warburg observed that tumor cells consumed a large amount of glucose, much more than normal cells, and converted most of it to lactic acid. This phenomenon, now known as the "Warburg effect," is the foundation of one of the earliest general concepts of cancer: that a fundamental disturbance of cellular metabolic activity is at the root of tumor formation and growth. In the ensuing decades, as it became apparent that abnormalities in chromosomes and eventually individual genes caused cancer, the "metabolic" model of cancer lost a good deal of its appeal, even as emerging technologies were exploiting the Warburg effect clinically to detect tumors in vivo. We now know that tumor suppressors and proto-oncogenes influence metabolism, and that mutations in these genes can promote a metabolic phenotype supporting cell growth and proliferation. Thus, these advances have unified aspects of the metabolic and genetic models of cancer, and have stimulated a renewed interest in the role of cellular metabolism in tumorigenesis. This review reappraises the notion that dysregulated cellular metabolism is a key feature of cancer, and discusses some metabolic issues that have escaped scrutiny over the years and now deserve closer attention. Genet Med 2008:10(11):767-777.
引用
收藏
页码:267 / 277
页数:11
相关论文
共 102 条
[71]   A functional screen for Myc-responsive genes reveals serine hydroxymethyltransferase, a major source of the one-carbon unit for cell metabolism [J].
Nikiforov, MA ;
Chandriani, S ;
O'Connell, B ;
Petrenko, O ;
Kotenko, I ;
Beavis, A ;
Sedivy, JM ;
Cole, MD .
MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (16) :5793-5800
[72]   LIVER AND ADIPOSE-TISSUE CONTRIBUTIONS TO NEWLY FORMED FATTY-ACIDS IN AN ASCITES TUMOR [J].
OOKHTENS, M ;
KANNAN, R ;
LYON, I ;
BAKER, N .
AMERICAN JOURNAL OF PHYSIOLOGY, 1984, 247 (01) :R146-R153
[73]  
OVEJERA AA, 1979, CANCER RES, V39, P3220
[74]   Distinct mitochondrial retrograde signals control the G1-S cell cycle checkpoint [J].
Owusu-Ansah, Edward ;
Yavari, Amir ;
Mandal, Sudip ;
Banerjee, Utpal .
NATURE GENETICS, 2008, 40 (03) :356-361
[75]   HIF-1 mediates adaptation to hypoxia by actively downregulating mitochondrial oxygen consumption [J].
Papandreou, I ;
Cairns, RA ;
Fontana, L ;
Lim, AL ;
Denko, NC .
CELL METABOLISM, 2006, 3 (03) :187-197
[76]  
PARLO RA, 1984, J BIOL CHEM, V259, P9997
[77]   CONTINUOUS PYRUVATE CARBON FLUX TO NEWLY SYNTHESIZED CHOLESTEROL AND THE SUPPRESSED EVOLUTION OF PYRUVATE-GENERATED CO2 IN TUMORS - FURTHER EVIDENCE FOR A PERSISTENT TRUNCATED KREBS CYCLE IN HEPATOMAS [J].
PARLO, RA ;
COLEMAN, PS .
BIOCHIMICA ET BIOPHYSICA ACTA, 1986, 886 (02) :169-176
[78]   An integrated genomic analysis of human glioblastoma Multiforme [J].
Parsons, D. Williams ;
Jones, Sian ;
Zhang, Xiaosong ;
Lin, Jimmy Cheng-Ho ;
Leary, Rebecca J. ;
Angenendt, Philipp ;
Mankoo, Parminder ;
Carter, Hannah ;
Siu, I-Mei ;
Gallia, Gary L. ;
Olivi, Alessandro ;
McLendon, Roger ;
Rasheed, B. Ahmed ;
Keir, Stephen ;
Nikolskaya, Tatiana ;
Nikolsky, Yuri ;
Busam, Dana A. ;
Tekleab, Hanna ;
Diaz, Luis A., Jr. ;
Hartigan, James ;
Smith, Doug R. ;
Strausberg, Robert L. ;
Marie, Suely Kazue Nagahashi ;
Shinjo, Sueli Mieko Oba ;
Yan, Hai ;
Riggins, Gregory J. ;
Bigner, Darell D. ;
Karchin, Rachel ;
Papadopoulos, Nick ;
Parmigiani, Giovanni ;
Vogelstein, Bert ;
Velculescu, Victor E. ;
Kinzler, Kenneth W. .
SCIENCE, 2008, 321 (5897) :1807-1812
[79]   RETRACTED: Frequent genetic and biochemical alterations of the PI3-K/AKT/PTEN pathway in head and neck squamous cell carcinoma (Retracted Article) [J].
Pedrero, JMG ;
Carracedo, DG ;
Pinto, CM ;
Zapatero, AH ;
Rodrigo, JP ;
Nieto, CS ;
Gonzalez, MV .
INTERNATIONAL JOURNAL OF CANCER, 2005, 114 (02) :242-248
[80]   mtDNA mutations increase tumorigenicity in prostate cancer [J].
Petros, JA ;
Baumann, AK ;
Ruiz-Pesini, E ;
Amin, MB ;
Sun, CQ ;
Hall, J ;
Lim, S ;
Issa, MM ;
Flanders, WD ;
Hosseini, SH ;
Marshall, FF ;
Wallace, DC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (03) :719-724