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Dissecting the Role of Autophagy-Related Proteins in Cancer Metabolism and Plasticity

Modulation of autophagy as an anticancer strategy has been widely studied and evaluated in several cell models. However, little attention has been paid to the metabolic changes that occur in a cancer cell when autophagy is inhibited or induced. In this review, we describe how the expression and regu...

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Autores principales: Torres-López, Liliana, Dobrovinskaya, Oxana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10605719/
https://www.ncbi.nlm.nih.gov/pubmed/37887330
http://dx.doi.org/10.3390/cells12202486
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author Torres-López, Liliana
Dobrovinskaya, Oxana
author_facet Torres-López, Liliana
Dobrovinskaya, Oxana
author_sort Torres-López, Liliana
collection PubMed
description Modulation of autophagy as an anticancer strategy has been widely studied and evaluated in several cell models. However, little attention has been paid to the metabolic changes that occur in a cancer cell when autophagy is inhibited or induced. In this review, we describe how the expression and regulation of various autophagy-related (ATGs) genes and proteins are associated with cancer progression and cancer plasticity. We present a comprehensive review of how deregulation of ATGs affects cancer cell metabolism, where inhibition of autophagy is mainly reflected in the enhancement of the Warburg effect. The importance of metabolic changes, which largely depend on the cancer type and form part of a cancer cell’s escape strategy after autophagy modulation, is emphasized. Consequently, pharmacological strategies based on a dual inhibition of metabolic and autophagy pathways emerged and are reviewed critically here.
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spelling pubmed-106057192023-10-28 Dissecting the Role of Autophagy-Related Proteins in Cancer Metabolism and Plasticity Torres-López, Liliana Dobrovinskaya, Oxana Cells Review Modulation of autophagy as an anticancer strategy has been widely studied and evaluated in several cell models. However, little attention has been paid to the metabolic changes that occur in a cancer cell when autophagy is inhibited or induced. In this review, we describe how the expression and regulation of various autophagy-related (ATGs) genes and proteins are associated with cancer progression and cancer plasticity. We present a comprehensive review of how deregulation of ATGs affects cancer cell metabolism, where inhibition of autophagy is mainly reflected in the enhancement of the Warburg effect. The importance of metabolic changes, which largely depend on the cancer type and form part of a cancer cell’s escape strategy after autophagy modulation, is emphasized. Consequently, pharmacological strategies based on a dual inhibition of metabolic and autophagy pathways emerged and are reviewed critically here. MDPI 2023-10-19 /pmc/articles/PMC10605719/ /pubmed/37887330 http://dx.doi.org/10.3390/cells12202486 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Torres-López, Liliana
Dobrovinskaya, Oxana
Dissecting the Role of Autophagy-Related Proteins in Cancer Metabolism and Plasticity
title Dissecting the Role of Autophagy-Related Proteins in Cancer Metabolism and Plasticity
title_full Dissecting the Role of Autophagy-Related Proteins in Cancer Metabolism and Plasticity
title_fullStr Dissecting the Role of Autophagy-Related Proteins in Cancer Metabolism and Plasticity
title_full_unstemmed Dissecting the Role of Autophagy-Related Proteins in Cancer Metabolism and Plasticity
title_short Dissecting the Role of Autophagy-Related Proteins in Cancer Metabolism and Plasticity
title_sort dissecting the role of autophagy-related proteins in cancer metabolism and plasticity
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10605719/
https://www.ncbi.nlm.nih.gov/pubmed/37887330
http://dx.doi.org/10.3390/cells12202486
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