A glutamine ‘tug-of-war’: targets to manipulate glutamine metabolism for cancer immunotherapy

Author:

Pallett Laura J1ORCID,Dimeloe Sarah2,Sinclair Linda V3ORCID,Byrne Adam J4,Schurich Anna5ORCID

Affiliation:

1. Division of Infection and Immunity, Institute of Immunity and Transplantation, University College London, London, UK

2. Institute of Immunology and Immunotherapy, Institute of Metabolism and Systems Research, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK

3. Division of Cell Signalling and Immunology, School of Life Sciences, University of Dundee, Dundee, UK

4. Inflammation, Repair and Development Section, National Heart and Lung Institute, Imperial College London, London, UK

5. Department of Infectious Diseases, School of Immunology and Microbial Sciences, King’s College London, London, UK

Abstract

Summary Within the tumour microenvironment (TME), there is a cellular ‘tug-of-war’ for glutamine, the most abundant amino acid in the body. This competition is most evident when considering the balance between a successful anti-tumour immune response and the uncontrolled growth of tumour cells that are addicted to glutamine. The differential effects of manipulating glutamine abundance in individual cell types is an area of intense research and debate. Here, we discuss some of the current strategies in development altering local glutamine availability focusing on inhibition of enzymes involved in the utilisation of glutamine and its uptake by cells in the TME. Further studies are urgently needed to complete our understanding of glutamine metabolism, to provide critical insights into the pathways that represent promising targets and for the development of novel therapeutic strategies for the treatment of advanced or drug resistant cancers.

Funder

Wellcome Trust

Cancer Research UK

Leukaemia UK

Publisher

Oxford University Press (OUP)

Subject

General Medicine

Reference75 articles.

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4. Autophagy is required for PDAC glutamine metabolism;Seo;Sci Rep,2016

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