Glutaminase - A potential target for cancer treatment

被引:4
作者
Anthony, Josephine [1 ]
Varalakshmi, Sureka [1 ]
Sekar, Ashok Kumar [2 ]
Devarajan, Nalini [1 ]
Janakiraman, Balamurugan [3 ]
Peramaiyan, Rajendran [4 ,5 ]
机构
[1] MAHER Deemed Be Univ, Meenakshi Acad Higher Educ & Res, Dept Res, Chennai 600078, Tamil Nadu, India
[2] Anna Univ, Ctr Biotechnol, Chennai 600025, Tamil Nadu, India
[3] SRM Inst Sci & Technol SRMIST, Fac Med & Hlth Sci, SRM Coll Physiotherapy, Kattankulathur 603203, Tamil Nadu, India
[4] King Faisal Univ, Coll Sci, Dept Biol Sci, Al Hasa 31982, Saudi Arabia
[5] Saveetha Univ, Saveetha Dent Coll & Hosp, Ctr Mol Med & Diagnost COMManD, Dept Biochem, Chennai 600077, Tamil Nadu, India
来源
BIOMEDICINE-TAIWAN | 2024年 / 14卷 / 02期
关键词
Glutamine; Cancer; Glutaminase inhibitor; Glutaminase; Autophagy; Redox homeostasis; CELL-PROLIFERATION; OXIDATIVE-PHOSPHORYLATION; MITOCHONDRIAL METABOLISM; AUTOPHAGY; INHIBITION; MTORC1; PROLINE; GROWTH; CONTRIBUTES; EXPRESSION;
D O I
10.37796/2211-8039.1445
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The overexpression of glutaminase is reported to influence cancer growth and metastasis through glutaminolysis. Upregulation of glutamine catabolism is recently recognized as a critical feature of cancer, and cancer cells are observed to reprogram glutamine metabolism to maintain its survival and proliferation. Special focus is given on the glutaminase isoform, GLS1 (kidney type glutaminase), as the other isoform GLS2 (Liver type glutaminase) acts as a tumour suppressor in some conditions. Glutaminolysis linked with autophagy, which is mediated via mTORC1, also serves as a promising target for cancer therapy. Glutamine also plays a vital role in maintaining redox homeostasis. Inhibition of glutaminase aggravates oxidative stress by reducing glutathione level, thus leading to apoptotic-mediated cell death in cancer cells Therefore, inhibiting the glutaminase activity using glutaminase inhibitors such as BPTES, DON, JHU-083, CB-839, compound 968, etc. may answer many intriguing questions behind the uncontrolled proliferation of cancer cells and serve as a prophylactic treatment for cancer. Earlier reports neither discuss nor provide perspectives on exact signaling gene or pathway. Hence, the present review highlights the plausible role of glutaminase in cancer and the current therapeutic approaches and clinical trials to target and inhibit glutaminase enzymes for better cancer treatment.
引用
收藏
页码:29 / 37
页数:9
相关论文
共 74 条
[1]   Role of AMPK-mTOR-Ulk1/2 in the Regulation of Autophagy: Cross Talk, Shortcuts, and Feedbacks [J].
Alers, Sebastian ;
Loeffler, Antje S. ;
Wesselborg, Sebastian ;
Stork, Bjoern .
MOLECULAR AND CELLULAR BIOLOGY, 2012, 32 (01) :2-11
[2]   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
[3]   Regulation of mTORC1 by amino acids [J].
Bar-Peled, Liron ;
Sabatini, David M. .
TRENDS IN CELL BIOLOGY, 2014, 24 (07) :400-406
[4]   PHOSPHORYLATION OF RIBOSOMAL-PROTEIN S6 IS INHIBITORY FOR AUTOPHAGY IN ISOLATED RAT HEPATOCYTES [J].
BLOMMAART, EFC ;
LUIKEN, JJFP ;
BLOMMAART, PJE ;
VANWOERKOM, GM ;
MEIJER, AJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (05) :2320-2326
[5]   Glutamine, MTOR and autophagy: a multiconnection relationship [J].
Bodineau, Clement ;
Tome, Mercedes ;
Murdoch, Piedad del Socorro ;
Duran, Raul V. .
AUTOPHAGY, 2022, 18 (11) :2749-2750
[6]   Two parallel pathways connect glutamine metabolism and mTORC1 activity to regulate glutamoptosis [J].
Bodineau, Clement ;
Tome, Mercedes ;
Courtois, Sarah ;
Costa, Ana S. H. ;
Sciacovelli, Marco ;
Rousseau, Benoit ;
Richard, Elodie ;
Vacher, Pierre ;
Parejo-Perez, Carlos ;
Bessede, Emilie ;
Varon, Christine ;
Soubeyran, Pierre ;
Frezza, Christian ;
Murdoch, Piedad del Socorro ;
Villar, Victor H. ;
Duran, Raul, V .
NATURE COMMUNICATIONS, 2021, 12 (01)
[7]   Prolyl hydroxylases as regulators of cell metabolism [J].
Boulahbel, Houda ;
Duran, Raul V. ;
Gottlieb, Eyal .
BIOCHEMICAL SOCIETY TRANSACTIONS, 2009, 37 :291-294
[8]   Alanyl-glutamine consumption modifies the suppressive effect of L-asparaginase on lymphocyte Populations in mice1,2 [J].
Bunpo, Piyawan ;
Murray, Betty ;
Cundiff, Judy ;
Brizius, Emma ;
Aldrich, Carla J. ;
Anthony, Tracy G. .
JOURNAL OF NUTRITION, 2008, 138 (02) :338-343
[9]   The mTORC1 Pathway Stimulates Glutamine Metabolism and Cell Proliferation by Repressing SIRT4 [J].
Csibi, Alfred ;
Fendt, Sarah-Maria ;
Li, Chenggang ;
Poulogiannis, George ;
Choo, Andrew Y. ;
Chapski, Douglas J. ;
Jeong, Seung Min ;
Dempsey, Jamie M. ;
Parkhitko, Andrey ;
Morrison, Tasha ;
Henske, Elizabeth P. ;
Haigis, Marcia C. ;
Cantley, Lewis C. ;
Stephanopoulos, Gregory ;
Yu, Jane ;
Blenis, John .
CELL, 2013, 153 (04) :840-854
[10]   Full-Length Human Glutaminase in Complex with an Allosteric Inhibitor [J].
DeLaBarre, Byron ;
Gross, Stefan ;
Fang, Cheng ;
Gao, Yi ;
Jha, Abhishek ;
Jiang, Fan ;
Song, Juanhua J. ;
Wei, Wentao ;
Hurov, Jonathan B. .
BIOCHEMISTRY, 2011, 50 (50) :10764-10770