Cancer-generated lactic acid: a regulatory, immunosuppressive metabolite?

被引:249
作者
Choi, Stephen Yiu Chuen [1 ]
Collins, Colin C. [2 ,3 ]
Gout, Peter W. [1 ]
Wang, Yuzhuo [1 ,2 ,3 ]
机构
[1] BC Canc Agcy, Dept Expt Therapeut, Vancouver, BC V5Z 1L3, Canada
[2] Univ British Columbia, Fac Med, Dept Urol Sci, Vancouver, BC, Canada
[3] Vancouver Prostate Ctr, Vancouver, BC, Canada
基金
中国国家自然科学基金; 加拿大健康研究院;
关键词
Warburg effect; aerobic glycolysis; glutaminolysis; lactic acid; immune suppression; tumour micro-environment; ENDOTHELIAL-CELL METABOLISM; LDH-A; TUMOR; LACTATE; PH; INHIBITION; GLUTAMINE; GLYCOLYSIS; GLUCOSE; CD147;
D O I
10.1002/path.4218
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The common preference of cancers for lactic acid-generating metabolic energy pathways has led to proposals that their reprogrammed metabolism confers growth advantages such as decreased susceptibility to hypoxic stress. Recent observations, however, suggest that it generates a novel way for cancer survival. There is increasing evidence that cancers can escape immune destruction by suppressing the anti-cancer immune response through maintaining a relatively low pH in their micro-environment. Tumours achieve this by regulating lactic acid secretion via modification of glucose/glutamine metabolisms. We propose that the maintenance by cancers of a relatively low pH in their micro-environment, via regulation of their lactic acid secretion through selective modification of their energy metabolism, is another major mechanism by which cancers can suppress the anti-cancer immune response. Cancer-generated lactic acid could thus be viewed as a critical, immunosuppressive metabolite in the tumour micro-environment rather than a waste product'. This paradigm shift can have major impact on therapeutic strategy development. Copyright (c) 2013 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
引用
收藏
页码:350 / 355
页数:6
相关论文
共 53 条
[21]   Hallmarks of Cancer: The Next Generation [J].
Hanahan, Douglas ;
Weinberg, Robert A. .
CELL, 2011, 144 (05) :646-674
[22]   Endothelial cell metabolism and implications for cancer therapy [J].
Harjes, U. ;
Bensaad, K. ;
Harris, A. L. .
BRITISH JOURNAL OF CANCER, 2012, 107 (08) :1207-1212
[23]   Understanding the Warburg Effect: The Metabolic Requirements of Cell Proliferation [J].
Heiden, Matthew G. Vander ;
Cantley, Lewis C. ;
Thompson, Craig B. .
SCIENCE, 2009, 324 (5930) :1029-1033
[24]   Lactate: A Metabolic Key Player in Cancer [J].
Hirschhaeuser, Franziska ;
Sattler, Ulrike G. A. ;
Mueller-Klieser, Wolfgang .
CANCER RESEARCH, 2011, 71 (22) :6921-6925
[25]   Cancer cell metabolism: Warburg and beyond [J].
Hsu, Peggy P. ;
Sabatini, David M. .
CELL, 2008, 134 (05) :703-707
[26]   Cellular pH regulators: potentially promising molecular targets for cancer chemotherapy [J].
Izumi, H ;
Torigoe, T ;
Ishiguchi, H ;
Uramoto, H ;
Yoshida, Y ;
Tanabe, M ;
Ise, T ;
Murakami, T ;
Yoshida, T ;
Nomoto, M ;
Kohno, K .
CANCER TREATMENT REVIEWS, 2003, 29 (06) :541-549
[27]   18F-FDG Uptake in Lung, Breast, and Colon Cancers: Molecular Biology Correlates and Disease Characterization [J].
Jadvar, Hossein ;
Alavi, Abass ;
Gambhir, Sanjiv S. .
JOURNAL OF NUCLEAR MEDICINE, 2009, 50 (11) :1820-1827
[28]  
Kellum J A, 2004, Crit Care Resusc, V6, P197
[29]   Lactic and hydrochloric acids induce different patterns of inflammatory response in LPS-stimulated RAW 264.7 cells [J].
Kellum, JA ;
Song, MC ;
Li, JY .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2004, 286 (04) :R686-R692
[30]   Carbohydrate restriction and lactate transporter inhibition in a mouse xenograft model of human prostate cancer [J].
Kim, Howard S. ;
Masko, Elizabeth M. ;
Poulton, Susan L. ;
Kennedy, Kelly M. ;
Pizzo, Salvatore V. ;
Dewhirst, Mark W. ;
Freedland, Stephen J. .
BJU INTERNATIONAL, 2012, 110 (07) :1062-1069