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The acidic tumor microenvironment drives a stem-like phenotype in melanoma cells
ABSTRACT: Acidosis characterizes the microenvironment of most solid tumors and is considered a new hallmark of cancer. It is mainly caused by both “aerobic” and “anaerobic” glycolysis of differently adapted cancer cells, with the final product lactic acid being responsible of the extracellular acidi...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7525286/ https://www.ncbi.nlm.nih.gov/pubmed/32803272 http://dx.doi.org/10.1007/s00109-020-01959-y |
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author | Andreucci, Elena Peppicelli, Silvia Ruzzolini, Jessica Bianchini, Francesca Biagioni, Alessio Papucci, Laura Magnelli, Lucia Mazzanti, Benedetta Stecca, Barbara Calorini, Lido |
author_facet | Andreucci, Elena Peppicelli, Silvia Ruzzolini, Jessica Bianchini, Francesca Biagioni, Alessio Papucci, Laura Magnelli, Lucia Mazzanti, Benedetta Stecca, Barbara Calorini, Lido |
author_sort | Andreucci, Elena |
collection | PubMed |
description | ABSTRACT: Acidosis characterizes the microenvironment of most solid tumors and is considered a new hallmark of cancer. It is mainly caused by both “aerobic” and “anaerobic” glycolysis of differently adapted cancer cells, with the final product lactic acid being responsible of the extracellular acidification. Many evidences underline the role of extracellular acidosis in tumor progression. Among the different findings, we demonstrated that acidosis-exposed cancer cells are characterized by an epithelial-to-mesenchymal transition phenotype with high invasive ability, high resistance to apoptosis, anchorage-independent growth, and drug therapy. Acidic melanoma cells over-express SOX2, which is crucial for the maintenance of their oxidative metabolism, and carbonic anhydrase IX, that correlates with poor prognosis of cancer patients. Considering these evidences, we realized that the profile outlined for acid cancer cells inevitably remind us the stemness profile. Therefore, we wondered whether extracellular acidosis might induce in cancer cells the acquisition of stem-like properties and contribute to the expansion of the cancer stem cell sub-population. We found that a chronic adaptation to acidosis stimulates in cancer cells the expression of stem-related markers, also providing a high in vitro/in vivo clonogenic and trans-differentiating ability. Moreover, we observed that the acidosis-induced stem-like phenotype of melanoma cells was reversible and related to the EMT induction. These findings help to characterize a further aspect of stem cell niche, contributing to the sustainment and expansion of cancer stem cell subpopulation. Thus, the usage of agents controlling tumor extracellular acidosis might acquire great importance in the clinic for the treatment of aggressive solid tumor. KEY MESSAGES: • Extracellular acidosis up-regulates EMT and stem-related markers in melanoma cells • Acidic medium up-regulates in vitro self-renewal capacity of melanoma cells • Chronic acidosis adaptation induces trans-differentiation ability in melanoma cells • Melanoma cells adapted to acidosis show higher tumor-initiating potential than control cells • Extracellular acidosis promotes a stem-like phenotype in prostate and colorectal carcinoma cells |
format | Online Article Text |
id | pubmed-7525286 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-75252862020-10-14 The acidic tumor microenvironment drives a stem-like phenotype in melanoma cells Andreucci, Elena Peppicelli, Silvia Ruzzolini, Jessica Bianchini, Francesca Biagioni, Alessio Papucci, Laura Magnelli, Lucia Mazzanti, Benedetta Stecca, Barbara Calorini, Lido J Mol Med (Berl) Original Article ABSTRACT: Acidosis characterizes the microenvironment of most solid tumors and is considered a new hallmark of cancer. It is mainly caused by both “aerobic” and “anaerobic” glycolysis of differently adapted cancer cells, with the final product lactic acid being responsible of the extracellular acidification. Many evidences underline the role of extracellular acidosis in tumor progression. Among the different findings, we demonstrated that acidosis-exposed cancer cells are characterized by an epithelial-to-mesenchymal transition phenotype with high invasive ability, high resistance to apoptosis, anchorage-independent growth, and drug therapy. Acidic melanoma cells over-express SOX2, which is crucial for the maintenance of their oxidative metabolism, and carbonic anhydrase IX, that correlates with poor prognosis of cancer patients. Considering these evidences, we realized that the profile outlined for acid cancer cells inevitably remind us the stemness profile. Therefore, we wondered whether extracellular acidosis might induce in cancer cells the acquisition of stem-like properties and contribute to the expansion of the cancer stem cell sub-population. We found that a chronic adaptation to acidosis stimulates in cancer cells the expression of stem-related markers, also providing a high in vitro/in vivo clonogenic and trans-differentiating ability. Moreover, we observed that the acidosis-induced stem-like phenotype of melanoma cells was reversible and related to the EMT induction. These findings help to characterize a further aspect of stem cell niche, contributing to the sustainment and expansion of cancer stem cell subpopulation. Thus, the usage of agents controlling tumor extracellular acidosis might acquire great importance in the clinic for the treatment of aggressive solid tumor. KEY MESSAGES: • Extracellular acidosis up-regulates EMT and stem-related markers in melanoma cells • Acidic medium up-regulates in vitro self-renewal capacity of melanoma cells • Chronic acidosis adaptation induces trans-differentiation ability in melanoma cells • Melanoma cells adapted to acidosis show higher tumor-initiating potential than control cells • Extracellular acidosis promotes a stem-like phenotype in prostate and colorectal carcinoma cells Springer Berlin Heidelberg 2020-08-15 2020 /pmc/articles/PMC7525286/ /pubmed/32803272 http://dx.doi.org/10.1007/s00109-020-01959-y Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Original Article Andreucci, Elena Peppicelli, Silvia Ruzzolini, Jessica Bianchini, Francesca Biagioni, Alessio Papucci, Laura Magnelli, Lucia Mazzanti, Benedetta Stecca, Barbara Calorini, Lido The acidic tumor microenvironment drives a stem-like phenotype in melanoma cells |
title | The acidic tumor microenvironment drives a stem-like phenotype in melanoma cells |
title_full | The acidic tumor microenvironment drives a stem-like phenotype in melanoma cells |
title_fullStr | The acidic tumor microenvironment drives a stem-like phenotype in melanoma cells |
title_full_unstemmed | The acidic tumor microenvironment drives a stem-like phenotype in melanoma cells |
title_short | The acidic tumor microenvironment drives a stem-like phenotype in melanoma cells |
title_sort | acidic tumor microenvironment drives a stem-like phenotype in melanoma cells |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7525286/ https://www.ncbi.nlm.nih.gov/pubmed/32803272 http://dx.doi.org/10.1007/s00109-020-01959-y |
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