The Tricarboxylic Acid Cycle Metabolites for Cancer: Friend or Enemy

Author:

Wu Jie12345,Liu Nian12345,Chen Jing12345,Tao Qian12345,Li Qiuqiu12345,Li Jie12345,Chen Xiang12345,Peng Cong12345ORCID

Affiliation:

1. The Department of Dermatology, Xiangya Hospital, Central South University, Changsha, Hunan, China.

2. Furong Labratory, Changsha, Hunan, China.

3. Hunan Key Laboratory of Skin Cancer and Psoriasis, Hunan Engineering Research Center of Skin Health and Disease, Xiangya Hospital, Central South University, Changsha, Hunan, China.

4. National Engineering Research Center of Personalized Diagnostic and Therapeutic Technology, Changsha, Hunan, China.

5. National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, Hunan, China.

Abstract

The tricarboxylic acid (TCA) cycle is capable of providing sufficient energy for the physiological activities under aerobic conditions. Although tumor metabolic reprogramming places aerobic glycolysis in a dominant position, the TCA cycle remains indispensable for tumor cells as a hub for the metabolic linkage and interconversion of glucose, lipids, and certain amino acids. TCA intermediates such as citrate, α-ketoglutarate, succinate, and fumarate are altered in tumors, and they regulate the tumor metabolism, signal transduction, and immune environment to affect tumorigenesis and tumor progression. This article provides a comprehensive review of the modifications occurring in tumor cells in relation to the intermediates of the TCA cycle, which affects tumor pathogenesis and current therapeutic strategy for therapy through targeting TCA cycle in cancer cells.

Funder

National Natural Science Foundation of China

The Scientific Research Program of FuRong Laboratory

the science and technology innovation Program of Hunan Province

Publisher

American Association for the Advancement of Science (AAAS)

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