Metabolism of Amino Acids in Cancer

被引:281
作者
Wei, Zhen [1 ]
Liu, Xiaoyi [2 ]
Cheng, Chunming [3 ,4 ]
Yu, Wei [5 ]
Yi, Ping [2 ]
机构
[1] Wuhan Univ Sci & Technol, Hubei Prov Key Lab Occupat Hazard Identificat & C, Sch Med, Brain Sci & Adv Technol Inst, Wuhan, Peoples R China
[2] Chongqing Med Univ, Dept Obstet & Gynecol, Affiliated Hosp 3, Chongqing, Peoples R China
[3] Ohio State Univ, Dept Radiat Oncol, James Comprehens Canc Ctr, Columbus, OH 43210 USA
[4] Ohio State Univ, Coll Med, Columbus, OH 43210 USA
[5] Fudan Univ, Sch Life Sci, Zhongshan Hosp, State Key Lab Genet Engn, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
amino acids (AAs); metabolism; cancer; mTORC (mammalian target of rapamycin kinase complex); epigenetic; tumor immunity; ferroptosis; tumor growth; ONE-CARBON METABOLISM; TRANSPORTER; LAT1; ARGININOSUCCINATE SYNTHETASE EXPRESSION; TRANSFER-RNA SYNTHETASE; GLUTAMINE-METABOLISM; SERINE BIOSYNTHESIS; CELL-DEATH; ARGININE DEIMINASE; DNA METHYLATION; INDOLEAMINE 2,3-DIOXYGENASE;
D O I
10.3389/fcell.2020.603837
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Metabolic reprogramming has been widely recognized as a hallmark of malignancy. The uptake and metabolism of amino acids are aberrantly upregulated in many cancers that display addiction to particular amino acids. Amino acids facilitate the survival and proliferation of cancer cells under genotoxic, oxidative, and nutritional stress. Thus, targeting amino acid metabolism is becoming a potential therapeutic strategy for cancer patients. In this review, we will systematically summarize the recent progress of amino acid metabolism in malignancy and discuss their interconnection with mammalian target of rapamycin complex 1 (mTORC1) signaling, epigenetic modification, tumor growth and immunity, and ferroptosis. Finally, we will highlight the potential therapeutic applications.
引用
收藏
页数:23
相关论文
共 337 条
[1]   CAT-1-Mediated Arginine Uptake and Regulation of Nitric Oxide Synthases for the Survival of Human Breast Cancer Cell Lines [J].
Abdelmagid, Salma A. ;
Rickard, Jenaya A. ;
McDonald, William J. ;
Thomas, Lynn N. ;
Too, Catherine K. L. .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2011, 112 (04) :1084-1092
[2]   Phase III randomized study of second line ADI-PEG 20 plus best supportive care versus placebo plus best supportive care in patients with advanced hepatocellular carcinoma [J].
Abou-Alfa, G. K. ;
Qin, S. ;
Ryoo, B-Y. ;
Lu, S-N. ;
Yen, C-J. ;
Feng, Y-H. ;
Lim, H. Y. ;
Izzo, F. ;
Colombo, M. ;
Sarker, D. ;
Bolondi, L. ;
Vaccaro, G. ;
Harris, W. P. ;
Chen, Z. ;
Hubner, R. A. ;
Meyer, T. ;
Sun, W. ;
Harding, J. J. ;
Hollywood, E. M. ;
Ma, J. ;
Wan, P. J. ;
Ly, M. ;
Bomalaski, J. ;
Johnston, A. ;
Lin, C-C. ;
Chao, Y. ;
Chen, L-T. .
ANNALS OF ONCOLOGY, 2018, 29 (06) :1402-1408
[3]   Ivosidenib in IDH1-mutant, chemotherapy-refractory Croatia& cholangiocarcinoma (ClarlDHy): a multicentre, randomised, double-blind, placebo-controlled, phase 3 study [J].
Abou-Alfa, Ghassan K. ;
Macarulla, Teresa ;
Javle, Milind M. ;
Kelley, Robin K. ;
Lubner, Sam J. ;
Adeva, Jorge ;
Cleary, James M. ;
Catenacci, Daniel V. ;
Borad, Mitesh J. ;
Bridgewater, John ;
Harris, William P. ;
Murphy, Adrian G. ;
Oh, Do-Youn ;
Whisenant, Jonathan ;
Lowery, Maeve A. ;
Goyal, Lipika ;
Shroff, Rachna T. ;
El-Khoueiry, Anthony B. ;
Fan, Bin ;
Wu, Bin ;
Chamberlain, Christina X. ;
Jiang, Liewen ;
Gliser, Camelia ;
Pandya, Shuchi S. ;
Valle, Juan W. ;
Zhu, Andrew X. .
LANCET ONCOLOGY, 2020, 21 (06) :796-807
[4]   Lysine Acetylation Goes Global: From Epigenetics to Metabolism and Therapeutics [J].
Ali, Ibraheem ;
Conrad, Ryan J. ;
Verdin, Eric ;
Ott, Melanie .
CHEMICAL REVIEWS, 2018, 118 (03) :340-376
[5]   From Krebs to clinic: glutamine metabolism to cancer therapy [J].
Altman, Brian J. ;
Stine, Zachary E. ;
Dang, Chi V. .
NATURE REVIEWS CANCER, 2016, 16 (10) :619-634
[6]   IDH1 and IDH2 mutations are frequent events in central chondrosarcoma and central and periosteal chondromas but not in other mesenchymal tumours [J].
Amary, M. Fernanda ;
Bacsi, Krisztian ;
Maggiani, Francesca ;
Damato, Stephen ;
Halai, Dina ;
Berisha, Fitim ;
Pollock, Robin ;
O'Donnell, Paul ;
Grigoriadis, Anita ;
Diss, Tim ;
Eskandarpour, Malihe ;
Presneau, Nadege ;
Hogendoorn, Pancras C. W. ;
Futreal, Andrew ;
Tirabosco, Roberto ;
Flanagan, Adrienne M. .
JOURNAL OF PATHOLOGY, 2011, 224 (03) :334-343
[7]   A phase 1 study of romidepsin and pralatrexate reveals marked activity in relapsed and refractory T-cell lymphoma [J].
Amengual, Jennifer E. ;
Lichtenstein, Renee ;
Lue, Jennifer ;
Sawas, Ahmed ;
Deng, Changchun ;
Lichtenstein, Emily ;
Khan, Karen ;
Atkins, Laine ;
Rada, Aishling ;
Kim, Hye A. ;
Chiuzan, Codruta ;
Kalac, Matko ;
Marchi, Enrica ;
Falchi, Lorenzo ;
Francescone, Mark A. ;
Schwartz, Lawrence ;
Cremers, Serge ;
O'Connor, Owen A. .
BLOOD, 2018, 131 (04) :397-407
[8]   Ferroptosis Inhibition: Mechanisms and Opportunities [J].
Angeli, Jose Pedro Friedmann ;
Shah, Ron ;
Pratt, Derek A. ;
Conrad, Marcus .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2017, 38 (05) :489-498
[9]   Histone Modifications and Cancer [J].
Audia, James E. ;
Campbell, Robert M. .
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY, 2016, 8 (04)
[10]   Regulation of arginine transport by GCN2 eIF2 kinase is important for replication of the intracellular parasite Toxoplasma gondii [J].
Augusto, Leonardo ;
Amin, Parth H. ;
Wek, Ronald C. ;
Sullivan, William J., Jr. .
PLOS PATHOGENS, 2019, 15 (06)