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Alternative Energy: Breaking Down the Diverse Metabolic Features of Lung Cancers
Metabolic reprogramming is a hallmark of cancer initiation, progression, and relapse. From the initial observation that cancer cells preferentially ferment glucose to lactate, termed the Warburg effect, to emerging evidence indicating that metabolic heterogeneity and mitochondrial metabolism are als...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8566922/ https://www.ncbi.nlm.nih.gov/pubmed/34745994 http://dx.doi.org/10.3389/fonc.2021.757323 |
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author | Cargill, Kasey R. Hasken, William L. Gay, Carl M. Byers, Lauren A. |
author_facet | Cargill, Kasey R. Hasken, William L. Gay, Carl M. Byers, Lauren A. |
author_sort | Cargill, Kasey R. |
collection | PubMed |
description | Metabolic reprogramming is a hallmark of cancer initiation, progression, and relapse. From the initial observation that cancer cells preferentially ferment glucose to lactate, termed the Warburg effect, to emerging evidence indicating that metabolic heterogeneity and mitochondrial metabolism are also important for tumor growth, the complex mechanisms driving cancer metabolism remain vastly unknown. These unique shifts in metabolism must be further investigated in order to identify unique therapeutic targets for individuals afflicted by this aggressive disease. Although novel therapies have been developed to target metabolic vulnerabilities in a variety of cancer models, only limited efficacy has been achieved. In particular, lung cancer metabolism has remained relatively understudied and underutilized for the advancement of therapeutic strategies, however recent evidence suggests that lung cancers have unique metabolic preferences of their own. This review aims to provide an overview of essential metabolic mechanisms and potential therapeutic agents in order to increase evidence of targeted metabolic inhibition for the treatment of lung cancer, where novel therapeutics are desperately needed. |
format | Online Article Text |
id | pubmed-8566922 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85669222021-11-05 Alternative Energy: Breaking Down the Diverse Metabolic Features of Lung Cancers Cargill, Kasey R. Hasken, William L. Gay, Carl M. Byers, Lauren A. Front Oncol Oncology Metabolic reprogramming is a hallmark of cancer initiation, progression, and relapse. From the initial observation that cancer cells preferentially ferment glucose to lactate, termed the Warburg effect, to emerging evidence indicating that metabolic heterogeneity and mitochondrial metabolism are also important for tumor growth, the complex mechanisms driving cancer metabolism remain vastly unknown. These unique shifts in metabolism must be further investigated in order to identify unique therapeutic targets for individuals afflicted by this aggressive disease. Although novel therapies have been developed to target metabolic vulnerabilities in a variety of cancer models, only limited efficacy has been achieved. In particular, lung cancer metabolism has remained relatively understudied and underutilized for the advancement of therapeutic strategies, however recent evidence suggests that lung cancers have unique metabolic preferences of their own. This review aims to provide an overview of essential metabolic mechanisms and potential therapeutic agents in order to increase evidence of targeted metabolic inhibition for the treatment of lung cancer, where novel therapeutics are desperately needed. Frontiers Media S.A. 2021-10-21 /pmc/articles/PMC8566922/ /pubmed/34745994 http://dx.doi.org/10.3389/fonc.2021.757323 Text en Copyright © 2021 Cargill, Hasken, Gay and Byers https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Cargill, Kasey R. Hasken, William L. Gay, Carl M. Byers, Lauren A. Alternative Energy: Breaking Down the Diverse Metabolic Features of Lung Cancers |
title | Alternative Energy: Breaking Down the Diverse Metabolic Features of Lung Cancers |
title_full | Alternative Energy: Breaking Down the Diverse Metabolic Features of Lung Cancers |
title_fullStr | Alternative Energy: Breaking Down the Diverse Metabolic Features of Lung Cancers |
title_full_unstemmed | Alternative Energy: Breaking Down the Diverse Metabolic Features of Lung Cancers |
title_short | Alternative Energy: Breaking Down the Diverse Metabolic Features of Lung Cancers |
title_sort | alternative energy: breaking down the diverse metabolic features of lung cancers |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8566922/ https://www.ncbi.nlm.nih.gov/pubmed/34745994 http://dx.doi.org/10.3389/fonc.2021.757323 |
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