Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Turdo, Alice, Porcelli, Gaetana, D’Accardo, Caterina, Di Franco, Simone, Verona, Francesco, Forte, Stefano, Giuffrida, Dario, Memeo, Lorenzo, Todaro, Matilde, Stassi, Giorgio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
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
_version_ 1783557680334372864
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
work_keys_str_mv AT turdoalice metabolicescaperoutesofcancerstemcellsandtherapeuticopportunities
AT porcelligaetana metabolicescaperoutesofcancerstemcellsandtherapeuticopportunities
AT daccardocaterina metabolicescaperoutesofcancerstemcellsandtherapeuticopportunities
AT difrancosimone metabolicescaperoutesofcancerstemcellsandtherapeuticopportunities
AT veronafrancesco metabolicescaperoutesofcancerstemcellsandtherapeuticopportunities
AT fortestefano metabolicescaperoutesofcancerstemcellsandtherapeuticopportunities
AT giuffridadario metabolicescaperoutesofcancerstemcellsandtherapeuticopportunities
AT memeolorenzo metabolicescaperoutesofcancerstemcellsandtherapeuticopportunities
AT todaromatilde metabolicescaperoutesofcancerstemcellsandtherapeuticopportunities
AT stassigiorgio metabolicescaperoutesofcancerstemcellsandtherapeuticopportunities