Glutaminolysis Supplying carbon or nitrogen or both for cancer cells?

被引:215
作者
Dang, Chi V. [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
关键词
cancer metabolism; glutaminolysis; ammonia; aerobic glycolysis; glutaminase; glutamine synthetase; METABOLISM; GLUCOSE; LIVER; GLYCOLYSIS; EXPRESSION; LINES;
D O I
10.4161/cc.9.19.13302
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
A cancer cell comprising largely of carbon, hydrogen, oxygen, phosphorus, nitrogen and sulfur requires not only glucose, which is avidly transported and converted to lactate by aerobic glycolysis or the Warburg effect, but also glutamine as a major substrate. Glutamine and essential amino acids, such as methionine, provide energy through the TCA cycle as well as nitrogen, sulfur and carbon skeletons for growing and proliferating cancer cells. The interplay between utilization of glutamine and glucose is likely to depend on the genetic make-up of a cancer cell. While the MYC oncogene induces both aerobic glycolysis and glutaminolysis, activated beta-catenin induces glutamine synthesis in hepatocellular carcinoma. Cancer cells that have elevated glutamine synthetase can use glutamate and ammonia to synthesize glutamine and are hence not addicted to glutamine. As such, cancer cells have many degrees of freedom for re-programming cell metabolism, which with better understanding will result in novel therapeutic approaches.
引用
收藏
页码:3884 / 3886
页数:3
相关论文
共 26 条
[1]
DEVIANT ENERGETIC METABOLISM OF GLYCOLYTIC CANCER-CELLS [J].
BAGGETTO, LG .
BIOCHIMIE, 1992, 74 (11) :959-974
[2]
Liver Zonation Occurs Through a β-Catenin-Dependent, c-Myc-Independent Mechanism [J].
Burke, Zoe D. ;
Reed, Karen R. ;
Phesse, Toby J. ;
Sansom, Owen J. ;
Clarke, Alan R. ;
Tosh, David .
GASTROENTEROLOGY, 2009, 136 (07) :2316-2324
[3]
New targets of β-catenin signaling in the liver are involved in the glutamine metabolism [J].
Cadoret, A ;
Ovejero, C ;
Terris, B ;
Souil, E ;
Lévy, L ;
Lamers, WH ;
Kitajewski, J ;
Kahn, A ;
Perret, C .
ONCOGENE, 2002, 21 (54) :8293-8301
[4]
Rethinking the Warburg Effect with Myc Micromanaging Glutamine Metabolism [J].
Dang, Chi V. .
CANCER RESEARCH, 2010, 70 (03) :859-862
[5]
Brick by brick: metabolism and tumor cell growth [J].
DeBerardinis, Ralph J. ;
Sayed, Nabil ;
Ditsworth, Dara ;
Thompson, Craig B. .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2008, 18 (01) :54-61
[6]
Beyond aerobic glycolysis: Transformed cells can engage in glutamine metabolism that exceeds the requirement for protein and nucleotide synthesis [J].
DeBerardinis, Ralph J. ;
Mancuso, Anthony ;
Daikhin, Evgueni ;
Nissim, Ilana ;
Yudkoff, Marc ;
Wehrli, Suzanne ;
Thompson, Craig B. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (49) :19345-19350
[7]
Ammonia Derived from Glutaminolysis Is a Diffusible Regulator of Autophagy [J].
Eng, Christina H. ;
Yu, Ker ;
Lucas, Judy ;
White, Eileen ;
Abraham, Robert T. .
SCIENCE SIGNALING, 2010, 3 (119) :ra31
[8]
c-Myc suppression of miR-23a/b enhances mitochondrial glutaminase expression and glutamine metabolism [J].
Gao, Ping ;
Tchernyshyov, Irina ;
Chang, Tsung-Cheng ;
Lee, Yun-Sil ;
Kita, Kayoko ;
Ochi, Takafumi ;
Zeller, Karen I. ;
De Marzo, Angelo M. ;
Van Eyk, Jennifer E. ;
Mendell, Joshua T. ;
Dang, Chi V. .
NATURE, 2009, 458 (7239) :762-U100
[9]
Cancer cell metabolism: Warburg and beyond [J].
Hsu, Peggy P. ;
Sabatini, David M. .
CELL, 2008, 134 (05) :703-707
[10]
KOVACEVIC Z, 1972, CANCER RES, V32, P326