Literature DB >> 28292200

Therapeutic effects of methionine sulfoximine in multiple diseases include and extend beyond inhibition of glutamine synthetase.

William S A Brusilow1, Tyler J Peters1.   

Abstract

INTRODUCTION: Methionine sulfoximine (MSO), a well-characterized inhibitor of glutamine synthetase, displays significant therapeutic benefits in animal models for several human diseases. This amino acid might therefore be a viable candidate for drug development to treat diseases for which there are few effective therapies. Areas covered: We describe the effects of MSO on brain swelling occurring in overt hepatic encephalopathy resulting from liver failure, the effects of MSO on excitotoxic damage involved in amyotrophic lateral sclerosis (ALS) or resulting from stroke, and the effects of MSO on a model for an inflammatory immune response involved in a range of diseases. We conclude that these results imply the existence of another therapeutic target for MSO in addition to glutamine synthetase. Expert opinion: We summarize the various diseases for which MSO treatment might be a candidate for drug development. We discuss why MSO has limited enthusiasm in the scientific and medical communities for use in humans, with a rebuttal to those negative opinions. And we conclude that MSO should be considered a candidate drug to treat brain swelling involved in overt hepatic encephalopathy and diseases involving an inflammatory immune response.

Entities:  

Keywords:  ALS; Glutamine synthetase; hepatic encephalopathy; inflammation; methionine sulfoximine

Mesh:

Substances:

Year:  2017        PMID: 28292200     DOI: 10.1080/14728222.2017.1303484

Source DB:  PubMed          Journal:  Expert Opin Ther Targets        ISSN: 1472-8222            Impact factor:   6.902


  7 in total

1.  In vitro suppression of inflammatory cytokine response by methionine sulfoximine.

Authors:  Tyler J Peters; Amruta A Jambekar; William S A Brusilow
Journal:  J Inflamm (Lond)       Date:  2018-09-10       Impact factor: 4.981

2.  Glutamine synthetase is necessary for sarcoma adaptation to glutamine deprivation and tumor growth.

Authors:  Sameer H Issaq; Arnulfo Mendoza; Stephen D Fox; Lee J Helman
Journal:  Oncogenesis       Date:  2019-02-26       Impact factor: 7.485

Review 3.  Glutamine Synthetase as a Therapeutic Target for Cancer Treatment.

Authors:  Go Woon Kim; Dong Hoon Lee; Yu Hyun Jeon; Jung Yoo; So Yeon Kim; Sang Wu Lee; Ha Young Cho; So Hee Kwon
Journal:  Int J Mol Sci       Date:  2021-02-08       Impact factor: 5.923

4.  Azithromycin resistance mutations in Streptococcus pneumoniae as revealed by a chemogenomic screen.

Authors:  Hélène Gingras; Kévin Patron; Philippe Leprohon; Marc Ouellette
Journal:  Microb Genom       Date:  2020-11

5.  Pharmacological Vitamin C Treatment Impedes the Growth of Endogenous Glutamine-Dependent Cancers by Targeting Glutamine Synthetase.

Authors:  Yali Long; Jia Qiu; Bing Zhang; Peng He; Xinchong Shi; Qiao He; Zhifeng Chen; Wanqing Shen; Zhoulei Li; Xiangsong Zhang
Journal:  Front Pharmacol       Date:  2021-05-11       Impact factor: 5.810

6.  Inhibition of Glutamate Release, but Not of Glutamine Recycling to Glutamate, Is Involved in Delaying the Onset of Initial Lithium-Pilocarpine-Induced Seizures in Young Rats by a Non-Convulsive MSO Dose.

Authors:  Marek J Pawlik; Blanca I Aldana; Lautaro F Belfiori-Carrasco; Marta Obara-Michlewska; Mariusz P Popek; Anna Maria Czarnecka; Jan Albrecht
Journal:  Int J Mol Sci       Date:  2021-10-15       Impact factor: 5.923

7.  Penicillin induces alterations in glutamine metabolism in Streptococcus pneumoniae.

Authors:  Jessica Y El Khoury; Nancy Boucher; Michel G Bergeron; Philippe Leprohon; Marc Ouellette
Journal:  Sci Rep       Date:  2017-11-06       Impact factor: 4.379

  7 in total

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