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Interplay between Immune Checkpoint Proteins and Cellular Metabolism
被引:85
|作者:
Lim, Sangbin
[1
]
Phillips, Joshua B.
[1
]
da Silva, Luciana Madeira
[1
]
Zhou, Ming
[2
]
Fodstad, Oystein
[3
]
Owen, Laurie B.
[1
]
Tan, Ming
[1
]
机构:
[1] Univ S Alabama, Mitchell Canc Inst, Ctr Cell Death & Metab, Mobile, AL USA
[2] Cent S Univ, Canc Res Inst, Chinese Minist Educ, Key Lab Carcinogenesis & Canc Invas, Changsha, Hunan, Peoples R China
[3] Univ Oslo, Oslo Univ Hosp, Norwegian Radium Hosp, Dept Tumor Biol, Oslo, Norway
关键词:
CANCER-CELLS;
GLUCOSE-METABOLISM;
AEROBIC GLYCOLYSIS;
EXPRESSION;
ACTIVATION;
MECHANISMS;
BLOCKADE;
ANTIBODY;
THERAPY;
ACID;
D O I:
10.1158/0008-5472.CAN-16-1647
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
With the recent successes in immuno-oncology, renewed interest in the role of immune checkpoint modulators, such as the B7 family proteins, has escalated. The immune checkpoint proteins play a crucial role in the regulation of cellular immunity; however, their contribution to other aspects of cancer biology remains unclear. Accumulating evidence indicate that immune checkpoint proteins can regulate metabolic energetics of the tumor, the tumor microenvironment, and the tumor-specific immune response, leading to metabolic reprogramming of both malignant cells and immune cells involved in mounting and sustaining this response. Immune cell metabolism impacts the activation status of immune cells and ultimately the immune response in cancer. Tumor cells may deplete nutrients that immune cells require for optimal generation, expansion, and function. They may also generate toxic metabolites in the microenvironment or induce conserved inhibitory pathways that impair immune function and thus inhibit antitumor responses. In this review, we will discuss how cancer cells with altered expression of immune checkpoint proteins can potently inhibit immune function through the alteration of cellular and microenvironmental metabolism, providing a new perspective on the interplay between these pathways and offering a potential therapeutic intervention strategy in the treatment of malignant disease. (C)2017 AACR.
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页码:1245 / 1249
页数:5
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