Macropinocytosis of protein is an amino acid supply route in Ras-transformed cells

被引:1275
作者
Commisso, Cosimo [1 ]
Davidson, Shawn M. [2 ,3 ]
Soydaner-Azeloglu, Rengin G. [1 ]
Parker, Seth J. [4 ]
Kamphorst, Jurre J. [5 ]
Hackett, Sean [5 ]
Grabocka, Elda [1 ]
Nofal, Michel [5 ]
Drebin, Jeffrey A. [6 ]
Thompson, Craig B. [7 ]
Rabinowitz, Joshua D. [5 ]
Metallo, Christian M. [4 ]
Vander Heiden, Matthew G. [2 ,3 ,8 ]
Bar-Sagi, Dafna [1 ]
机构
[1] NYU, Sch Med, Dept Biochem & Mol Pharmacol, New York, NY 10016 USA
[2] MIT, Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
[3] MIT, Dept Biol, Cambridge, MA 02139 USA
[4] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA
[5] Princeton Univ, Carl Icahn Lab, Lewis Sigler Inst Integrat Genom, Princeton, NJ 08544 USA
[6] Hosp Univ Penn, Dept Surg, Philadelphia, PA 19104 USA
[7] Mem Sloan Kettering Canc Ctr, Canc Biol & Genet Program, New York, NY 10065 USA
[8] Dana Farber Canc Inst, Boston, MA 02115 USA
基金
加拿大健康研究院; 美国国家卫生研究院;
关键词
MASS ISOTOPOMER DISTRIBUTIONS; K-RAS; GLUTAMINE-METABOLISM; H-RAS; CANCER; SRC; FIBROBLASTS; CARCINOMA; PATHWAYS; GROWTH;
D O I
10.1038/nature12138
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Macropinocytosis is a highly conserved endocytic process by which extracellular fluid and its contents are internalized into cells through large, heterogeneous vesicles known as macropinosomes. Oncogenic Ras proteins have been shown to stimulate macropinocytosis but the functional contribution of this uptake mechanism to the transformed phenotype remains unknown(1-3). Here we show that Ras-transformed cells use macropinocytosis to transport extracellular protein into the cell. The internalized protein undergoes proteolytic degradation, yielding amino acids including glutamine that can enter central carbon metabolism. Accordingly, the dependence of Ras-transformed cells on free extracellular glutamine for growth can be suppressed by the macropinocytic uptake of protein. Consistent with macropinocytosis representing an important route of nutrient uptake in tumours, its pharmacological inhibition compromises the growth of Ras-transformed pancreatic tumour xenografts. These results identify macropinocytosis as a mechanism by which cancer cells support their unique metabolic needs and point to the possible exploitation of this process in the design of anticancer therapies.
引用
收藏
页码:633 / +
页数:6
相关论文
共 32 条
[1]   Accurate assessment of amino acid mass isotopomer distributions for metabolic flux analysis [J].
Antoniewicz, Maciek R. ;
Kelleher, Joanne K. ;
Stephanopoulos, Gregory .
ANALYTICAL CHEMISTRY, 2007, 79 (19) :7554-7559
[2]  
AOKI K, 1995, CANCER RES, V55, P3810
[3]   INDUCTION OF MEMBRANE RUFFLING AND FLUID-PHASE PINOCYTOSIS IN QUIESCENT FIBROBLASTS BY RAS PROTEINS [J].
BARSAGI, D ;
FERAMISCO, JR .
SCIENCE, 1986, 233 (4768) :1061-1068
[4]  
BOS JL, 1989, CANCER RES, V49, P4682
[5]   COMPLETE NUCLEOTIDE-SEQUENCES OF THE T24 HUMAN BLADDER-CARCINOMA ONCOGENE AND ITS NORMAL HOMOLOG [J].
CAPON, DJ ;
CHEN, EY ;
LEVINSON, AD ;
SEEBURG, PH ;
GOEDDEL, DV .
NATURE, 1983, 302 (5903) :33-37
[6]  
Fernandez CA, 1996, J MASS SPECTROM, V31, P255, DOI 10.1002/(SICI)1096-9888(199603)31:3<255::AID-JMS290>3.0.CO
[7]  
2-3
[8]   Oncogenic K-Ras decouples glucose and glutamine metabolism to support cancer cell growth [J].
Gaglio, Daniela ;
Metallo, Christian M. ;
Gameiro, Paulo A. ;
Hiller, Karsten ;
Danna, Lara Sala ;
Balestrieri, Chiara ;
Alberghina, Lilia ;
Stephanopoulos, Gregory ;
Chiaradonna, Ferdinando .
MOLECULAR SYSTEMS BIOLOGY, 2011, 7
[9]   Glutamine Deprivation Induces Abortive S-Phase Rescued by Deoxyribonucleotides in K-Ras Transformed Fibroblasts [J].
Gaglio, Daniela ;
Soldati, Chiara ;
Vanoni, Marco ;
Alberghina, Lilia ;
Chiaradonna, Ferdinando .
PLOS ONE, 2009, 4 (03)
[10]   Trp53R172H and KraSG12D cooperate to promote chromosomal instability and widely metastatic pancreatic ductal adenocarcinoma in mice [J].
Hingorani, SR ;
Wang, LF ;
Multani, AS ;
Combs, C ;
Deramaudt, TB ;
Hruban, RH ;
Rustgi, AK ;
Chang, S ;
Tuveson, DA .
CANCER CELL, 2005, 7 (05) :469-483