Metabolic reprogramming of T regulatory cells in the hypoxic tumor microenvironment

<p dir="ltr">Metabolic dysregulation in the hypoxic tumor microenvironment (TME) is considered as a hallmark of solid tumors, leading to changes in biosynthetic pathways favoring onset, survival and proliferation of malignant cells. Within the TME, hypoxic milieu favors metabolic rep...

وصف كامل

محفوظ في:
التفاصيل البيبلوغرافية
المؤلف الرئيسي: Varun Sasidharan Nair (5396393) (author)
مؤلفون آخرون: Reem Saleh (3513056) (author), Salman M. Toor (8854751) (author), Farhan S. Cyprian (11924492) (author), Eyad Elkord (5396390) (author)
منشور في: 2021
الموضوعات:
الوسوم: إضافة وسم
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author Varun Sasidharan Nair (5396393)
author2 Reem Saleh (3513056)
Salman M. Toor (8854751)
Farhan S. Cyprian (11924492)
Eyad Elkord (5396390)
author2_role author
author
author
author
author_facet Varun Sasidharan Nair (5396393)
Reem Saleh (3513056)
Salman M. Toor (8854751)
Farhan S. Cyprian (11924492)
Eyad Elkord (5396390)
author_role author
dc.creator.none.fl_str_mv Varun Sasidharan Nair (5396393)
Reem Saleh (3513056)
Salman M. Toor (8854751)
Farhan S. Cyprian (11924492)
Eyad Elkord (5396390)
dc.date.none.fl_str_mv 2021-02-03T03:00:00Z
dc.identifier.none.fl_str_mv 10.1007/s00262-020-02842-y
dc.relation.none.fl_str_mv https://figshare.com/articles/journal_contribution/Metabolic_reprogramming_of_T_regulatory_cells_in_the_hypoxic_tumor_microenvironment/25709139
dc.rights.none.fl_str_mv CC BY 4.0
info:eu-repo/semantics/openAccess
dc.subject.none.fl_str_mv Biomedical and clinical sciences
Oncology and carcinogenesis
T regulatory cells
Hypoxia
Tumor microenvironment
Metabolism
Glycolysis
Fatty acid metabolism
dc.title.none.fl_str_mv Metabolic reprogramming of T regulatory cells in the hypoxic tumor microenvironment
dc.type.none.fl_str_mv Text
Journal contribution
info:eu-repo/semantics/publishedVersion
text
contribution to journal
description <p dir="ltr">Metabolic dysregulation in the hypoxic tumor microenvironment (TME) is considered as a hallmark of solid tumors, leading to changes in biosynthetic pathways favoring onset, survival and proliferation of malignant cells. Within the TME, hypoxic milieu favors metabolic reprogramming of tumor cells, which subsequently affects biological properties of tumor-infiltrating immune cells. T regulatory cells (Tregs), including both circulating and tissue-resident cells, are particularly susceptible to hypoxic metabolic signaling that can reprogram their biological and physicochemical properties. Furthermore, metabolic reprogramming modifies Tregs to utilize alternative substrates and undergo a plethora of metabolic events to meet their energy demands. Major impact of this metabolic reprogramming can result in differentiation, survival, excessive secretion of immunosuppressive cytokines and proliferation of Tregs within the TME, which in turn dampen anti-tumor immune responses. Studies on fine-tuning of Treg metabolism are challenging due to heterogenicity of tissue-resident Tregs and their dynamic functions. In this review, we highlight tumor intrinsic and extrinsic factors, which can influence Treg metabolism in the hypoxic TME. Moreover, we focus on metabolic reprogramming of Tregs that could unveil potential regulatory networks favoring tumorigenesis/progression, and provide novel insights, including inhibitors against acetyl-coA carboxylase 1 and transforming growth factor beta into targeting Treg metabolism for therapeutic benefits.</p><p dir="ltr">Correction: Metabolic reprogramming of T regulatory cells in the hypoxic tumor microenvironment. <a href="https://dx.doi.org/10.1007/s00262-021-02999-0" target="_blank">https://dx.doi.org/10.1007/s00262-021-02999-0</a>, published online 07 July 2021.</p><h2>Other Information</h2><p dir="ltr">Published in: Cancer Immunology, Immunotherapy<br>License: <a href="https://creativecommons.org/licenses/by/4.0" target="_blank">https://creativecommons.org/licenses/by/4.0</a><br>See article on publisher's website: <a href="https://dx.doi.org/10.1007/s00262-020-02842-y" target="_blank">https://dx.doi.org/10.1007/s00262-020-02842-y</a></p>
eu_rights_str_mv openAccess
id Manara2_0f2995c103c61747b177f7651e551fae
identifier_str_mv 10.1007/s00262-020-02842-y
network_acronym_str Manara2
network_name_str Manara2
oai_identifier_str oai:figshare.com:article/25709139
publishDate 2021
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spelling Metabolic reprogramming of T regulatory cells in the hypoxic tumor microenvironmentVarun Sasidharan Nair (5396393)Reem Saleh (3513056)Salman M. Toor (8854751)Farhan S. Cyprian (11924492)Eyad Elkord (5396390)Biomedical and clinical sciencesOncology and carcinogenesisT regulatory cellsHypoxiaTumor microenvironmentMetabolismGlycolysisFatty acid metabolism<p dir="ltr">Metabolic dysregulation in the hypoxic tumor microenvironment (TME) is considered as a hallmark of solid tumors, leading to changes in biosynthetic pathways favoring onset, survival and proliferation of malignant cells. Within the TME, hypoxic milieu favors metabolic reprogramming of tumor cells, which subsequently affects biological properties of tumor-infiltrating immune cells. T regulatory cells (Tregs), including both circulating and tissue-resident cells, are particularly susceptible to hypoxic metabolic signaling that can reprogram their biological and physicochemical properties. Furthermore, metabolic reprogramming modifies Tregs to utilize alternative substrates and undergo a plethora of metabolic events to meet their energy demands. Major impact of this metabolic reprogramming can result in differentiation, survival, excessive secretion of immunosuppressive cytokines and proliferation of Tregs within the TME, which in turn dampen anti-tumor immune responses. Studies on fine-tuning of Treg metabolism are challenging due to heterogenicity of tissue-resident Tregs and their dynamic functions. In this review, we highlight tumor intrinsic and extrinsic factors, which can influence Treg metabolism in the hypoxic TME. Moreover, we focus on metabolic reprogramming of Tregs that could unveil potential regulatory networks favoring tumorigenesis/progression, and provide novel insights, including inhibitors against acetyl-coA carboxylase 1 and transforming growth factor beta into targeting Treg metabolism for therapeutic benefits.</p><p dir="ltr">Correction: Metabolic reprogramming of T regulatory cells in the hypoxic tumor microenvironment. <a href="https://dx.doi.org/10.1007/s00262-021-02999-0" target="_blank">https://dx.doi.org/10.1007/s00262-021-02999-0</a>, published online 07 July 2021.</p><h2>Other Information</h2><p dir="ltr">Published in: Cancer Immunology, Immunotherapy<br>License: <a href="https://creativecommons.org/licenses/by/4.0" target="_blank">https://creativecommons.org/licenses/by/4.0</a><br>See article on publisher's website: <a href="https://dx.doi.org/10.1007/s00262-020-02842-y" target="_blank">https://dx.doi.org/10.1007/s00262-020-02842-y</a></p>2021-02-03T03:00:00ZTextJournal contributioninfo:eu-repo/semantics/publishedVersiontextcontribution to journal10.1007/s00262-020-02842-yhttps://figshare.com/articles/journal_contribution/Metabolic_reprogramming_of_T_regulatory_cells_in_the_hypoxic_tumor_microenvironment/25709139CC BY 4.0info:eu-repo/semantics/openAccessoai:figshare.com:article/257091392021-02-03T03:00:00Z
spellingShingle Metabolic reprogramming of T regulatory cells in the hypoxic tumor microenvironment
Varun Sasidharan Nair (5396393)
Biomedical and clinical sciences
Oncology and carcinogenesis
T regulatory cells
Hypoxia
Tumor microenvironment
Metabolism
Glycolysis
Fatty acid metabolism
status_str publishedVersion
title Metabolic reprogramming of T regulatory cells in the hypoxic tumor microenvironment
title_full Metabolic reprogramming of T regulatory cells in the hypoxic tumor microenvironment
title_fullStr Metabolic reprogramming of T regulatory cells in the hypoxic tumor microenvironment
title_full_unstemmed Metabolic reprogramming of T regulatory cells in the hypoxic tumor microenvironment
title_short Metabolic reprogramming of T regulatory cells in the hypoxic tumor microenvironment
title_sort Metabolic reprogramming of T regulatory cells in the hypoxic tumor microenvironment
topic Biomedical and clinical sciences
Oncology and carcinogenesis
T regulatory cells
Hypoxia
Tumor microenvironment
Metabolism
Glycolysis
Fatty acid metabolism