@article{ce0043f93e244b42a0cd106a1a962a7e,
title = "Inhibition of glutaminolysis in combination with other therapies to improve cancer treatment",
abstract = "Targeting glutamine catabolism has been attracting more research attention on the development of successful cancer therapy. Catalytic enzymes such as glutaminase (GLS) in glutaminolysis, a series of biochemical reactions by which glutamine is converted to glutamate and then alpha-ketoglutarate, an intermediate of the tricarboxylic acid (TCA) cycle, can be targeted by small molecule inhibitors, some of which are undergoing early phase clinical trials and exhibiting promising safety profiles. However, resistance to glutaminolysis targeting treatments has been observed, necessitating the development of treatments to combat this resistance. One option is to use synergy drug combinations, which improve tumor chemotherapy's effectiveness and diminish drug resistance and side effects. This review will focus on studies involving the glutaminolysis pathway and diverse combination therapies with therapeutic implications.",
keywords = "Combination therapy, Glutaminase, Glutaminolysis, Metabolic reprogramming, Therapeutic resistance",
author = "Shen, {Yao An} and Chen, {Chi Long} and Huang, {Yi Hsuan} and Evans, {Emily Elizabeth} and Cheng, {Chun Chia} and Chuang, {Ya Jie} and Cissy Zhang and Anne Le",
note = "Funding Information: This review has been prepared on the basis of the research works carried out in the laboratory of A Le supported by the National Institutes of Health (NIH) Grants R01-CA193895 , R01-CA112314 (to AL). The work in the laboratory of YA Shen was supported by a TMU grant 108-5403-003-112 and a grant from the Ministry of Science and Technology , Taiwan ( MOST 109-2314-B-038-021-MY3 ). Special thanks to Dr. Arthur Cooper for his helpful suggestions. Publisher Copyright: {\textcopyright} 2021 The Author(s)",
year = "2021",
month = jun,
doi = "10.1016/j.cbpa.2021.01.006",
language = "English",
volume = "62",
pages = "64--81",
journal = "Current Opinion in Chemical Biology",
issn = "1367-5931",
publisher = "Elsevier Ltd",
}