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The Role of Metabolic Changes in Shaping the Fate of Cancer-Associated Adipose Stem Cells
Adipose tissue in physiological and in metabolically altered conditions (obesity, diabetes, metabolic syndrome) strictly interacts with the developing tumors both systemically and locally. In addition to the cancer-associated fibroblasts, adipose cells have also recently been described among the piv...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7242628/ https://www.ncbi.nlm.nih.gov/pubmed/32478073 http://dx.doi.org/10.3389/fcell.2020.00332 |
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author | Cantini, Giulia Di Franco, Alessandra Mannelli, Massimo Scimè, Anthony Maggi, Mario Luconi, Michaela |
author_facet | Cantini, Giulia Di Franco, Alessandra Mannelli, Massimo Scimè, Anthony Maggi, Mario Luconi, Michaela |
author_sort | Cantini, Giulia |
collection | PubMed |
description | Adipose tissue in physiological and in metabolically altered conditions (obesity, diabetes, metabolic syndrome) strictly interacts with the developing tumors both systemically and locally. In addition to the cancer-associated fibroblasts, adipose cells have also recently been described among the pivotal actors of the tumor microenvironment responsible for sustaining tumor development and progression. In particular, emerging evidence suggests that not only the mature adipocytes but also the adipose stem cells (ASCs) are able to establish a strict crosstalk with the tumour cells, thus resulting in a reciprocal reprogramming of both the tumor and adipose components. This review will focus on the metabolic changes induced by this interaction as a driver of fate determination occurring in cancer-associated ASCs (CA-ASCs) to support the tumor metabolic requirements. We will showcase the major role played by the metabolic changes occurring in the adipose tumor microenvironment that regulates ASC fate and consequently cancer progression. Our new results will also highlight the CA-ASC response in vitro by using a coculture system of primary ASCs grown with cancer cells originating from two different types of adrenal cancers [adrenocortical carcinoma (ACC) and pheochromocytoma]. In conclusion, the different factors involved in this crosstalk process will be analyzed and their effects on the adipocyte differentiation potential and functions of CA-ASCs will be discussed. |
format | Online Article Text |
id | pubmed-7242628 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72426282020-05-29 The Role of Metabolic Changes in Shaping the Fate of Cancer-Associated Adipose Stem Cells Cantini, Giulia Di Franco, Alessandra Mannelli, Massimo Scimè, Anthony Maggi, Mario Luconi, Michaela Front Cell Dev Biol Cell and Developmental Biology Adipose tissue in physiological and in metabolically altered conditions (obesity, diabetes, metabolic syndrome) strictly interacts with the developing tumors both systemically and locally. In addition to the cancer-associated fibroblasts, adipose cells have also recently been described among the pivotal actors of the tumor microenvironment responsible for sustaining tumor development and progression. In particular, emerging evidence suggests that not only the mature adipocytes but also the adipose stem cells (ASCs) are able to establish a strict crosstalk with the tumour cells, thus resulting in a reciprocal reprogramming of both the tumor and adipose components. This review will focus on the metabolic changes induced by this interaction as a driver of fate determination occurring in cancer-associated ASCs (CA-ASCs) to support the tumor metabolic requirements. We will showcase the major role played by the metabolic changes occurring in the adipose tumor microenvironment that regulates ASC fate and consequently cancer progression. Our new results will also highlight the CA-ASC response in vitro by using a coculture system of primary ASCs grown with cancer cells originating from two different types of adrenal cancers [adrenocortical carcinoma (ACC) and pheochromocytoma]. In conclusion, the different factors involved in this crosstalk process will be analyzed and their effects on the adipocyte differentiation potential and functions of CA-ASCs will be discussed. Frontiers Media S.A. 2020-05-15 /pmc/articles/PMC7242628/ /pubmed/32478073 http://dx.doi.org/10.3389/fcell.2020.00332 Text en Copyright © 2020 Cantini, Di Franco, Mannelli, Scimè, Maggi and Luconi. http://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 | Cell and Developmental Biology Cantini, Giulia Di Franco, Alessandra Mannelli, Massimo Scimè, Anthony Maggi, Mario Luconi, Michaela The Role of Metabolic Changes in Shaping the Fate of Cancer-Associated Adipose Stem Cells |
title | The Role of Metabolic Changes in Shaping the Fate of Cancer-Associated Adipose Stem Cells |
title_full | The Role of Metabolic Changes in Shaping the Fate of Cancer-Associated Adipose Stem Cells |
title_fullStr | The Role of Metabolic Changes in Shaping the Fate of Cancer-Associated Adipose Stem Cells |
title_full_unstemmed | The Role of Metabolic Changes in Shaping the Fate of Cancer-Associated Adipose Stem Cells |
title_short | The Role of Metabolic Changes in Shaping the Fate of Cancer-Associated Adipose Stem Cells |
title_sort | role of metabolic changes in shaping the fate of cancer-associated adipose stem cells |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7242628/ https://www.ncbi.nlm.nih.gov/pubmed/32478073 http://dx.doi.org/10.3389/fcell.2020.00332 |
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