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Metabolic Escape Routes of Cancer Stem Cells and Therapeutic Opportunities
Although improvement in early diagnosis and treatment ameliorated life expectancy of cancer patients, metastatic disease still lacks effective therapeutic approaches. Resistance to anticancer therapies stems from the refractoriness of a subpopulation of cancer cells—termed cancer stem cells (CSCs)—w...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7352619/ https://www.ncbi.nlm.nih.gov/pubmed/32486505 http://dx.doi.org/10.3390/cancers12061436 |
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author | Turdo, Alice Porcelli, Gaetana D’Accardo, Caterina Di Franco, Simone Verona, Francesco Forte, Stefano Giuffrida, Dario Memeo, Lorenzo Todaro, Matilde Stassi, Giorgio |
author_facet | Turdo, Alice Porcelli, Gaetana D’Accardo, Caterina Di Franco, Simone Verona, Francesco Forte, Stefano Giuffrida, Dario Memeo, Lorenzo Todaro, Matilde Stassi, Giorgio |
author_sort | Turdo, Alice |
collection | PubMed |
description | Although improvement in early diagnosis and treatment ameliorated life expectancy of cancer patients, metastatic disease still lacks effective therapeutic approaches. Resistance to anticancer therapies stems from the refractoriness of a subpopulation of cancer cells—termed cancer stem cells (CSCs)—which is endowed with tumor initiation and metastasis formation potential. CSCs are heterogeneous and diverge by phenotypic, functional and metabolic perspectives. Intrinsic as well as extrinsic stimuli dictated by the tumor microenvironment (TME)have critical roles in determining cell metabolic reprogramming from glycolytic toward an oxidative phenotype and vice versa, allowing cancer cells to thrive in adverse milieus. Crosstalk between cancer cells and the surrounding microenvironment occurs through the interchange of metabolites, miRNAs and exosomes that drive cancer cells metabolic adaptation. Herein, we identify the metabolic nodes of CSCs and discuss the latest advances in targeting metabolic demands of both CSCs and stromal cells with the scope of improving current therapies and preventing cancer progression. |
format | Online Article Text |
id | pubmed-7352619 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-73526192020-07-21 Metabolic Escape Routes of Cancer Stem Cells and Therapeutic Opportunities Turdo, Alice Porcelli, Gaetana D’Accardo, Caterina Di Franco, Simone Verona, Francesco Forte, Stefano Giuffrida, Dario Memeo, Lorenzo Todaro, Matilde Stassi, Giorgio Cancers (Basel) Review Although improvement in early diagnosis and treatment ameliorated life expectancy of cancer patients, metastatic disease still lacks effective therapeutic approaches. Resistance to anticancer therapies stems from the refractoriness of a subpopulation of cancer cells—termed cancer stem cells (CSCs)—which is endowed with tumor initiation and metastasis formation potential. CSCs are heterogeneous and diverge by phenotypic, functional and metabolic perspectives. Intrinsic as well as extrinsic stimuli dictated by the tumor microenvironment (TME)have critical roles in determining cell metabolic reprogramming from glycolytic toward an oxidative phenotype and vice versa, allowing cancer cells to thrive in adverse milieus. Crosstalk between cancer cells and the surrounding microenvironment occurs through the interchange of metabolites, miRNAs and exosomes that drive cancer cells metabolic adaptation. Herein, we identify the metabolic nodes of CSCs and discuss the latest advances in targeting metabolic demands of both CSCs and stromal cells with the scope of improving current therapies and preventing cancer progression. MDPI 2020-05-31 /pmc/articles/PMC7352619/ /pubmed/32486505 http://dx.doi.org/10.3390/cancers12061436 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Turdo, Alice Porcelli, Gaetana D’Accardo, Caterina Di Franco, Simone Verona, Francesco Forte, Stefano Giuffrida, Dario Memeo, Lorenzo Todaro, Matilde Stassi, Giorgio Metabolic Escape Routes of Cancer Stem Cells and Therapeutic Opportunities |
title | Metabolic Escape Routes of Cancer Stem Cells and Therapeutic Opportunities |
title_full | Metabolic Escape Routes of Cancer Stem Cells and Therapeutic Opportunities |
title_fullStr | Metabolic Escape Routes of Cancer Stem Cells and Therapeutic Opportunities |
title_full_unstemmed | Metabolic Escape Routes of Cancer Stem Cells and Therapeutic Opportunities |
title_short | Metabolic Escape Routes of Cancer Stem Cells and Therapeutic Opportunities |
title_sort | metabolic escape routes of cancer stem cells and therapeutic opportunities |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7352619/ https://www.ncbi.nlm.nih.gov/pubmed/32486505 http://dx.doi.org/10.3390/cancers12061436 |
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