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Emerging Therapeutic RNAs for the Targeting of Cancer Associated Fibroblasts

Tumor mass consists of a complex ensemble of malignant cancer cells and a wide variety of resident and infiltrating cells, secreted factors, and extracellular matrix proteins that are referred as tumor microenvironment (TME). Cancer associated fibroblasts (CAFs) are key TME components that support t...

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Detalles Bibliográficos
Autores principales: Santana-Viera, Laura, Ibba, Maria L., Rotoli, Deborah, Catuogno, Silvia, Esposito, Carla L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7352655/
https://www.ncbi.nlm.nih.gov/pubmed/32466591
http://dx.doi.org/10.3390/cancers12061365
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author Santana-Viera, Laura
Ibba, Maria L.
Rotoli, Deborah
Catuogno, Silvia
Esposito, Carla L.
author_facet Santana-Viera, Laura
Ibba, Maria L.
Rotoli, Deborah
Catuogno, Silvia
Esposito, Carla L.
author_sort Santana-Viera, Laura
collection PubMed
description Tumor mass consists of a complex ensemble of malignant cancer cells and a wide variety of resident and infiltrating cells, secreted factors, and extracellular matrix proteins that are referred as tumor microenvironment (TME). Cancer associated fibroblasts (CAFs) are key TME components that support tumor growth, generating a physical barrier against drugs and immune infiltration, and contributing to regulate malignant progression. Thus, it is largely accepted that therapeutic approaches aimed at hampering the interactions between tumor cells and CAFs can enhance the effectiveness of anti-cancer treatments. In this view, nucleic acid therapeutics have emerged as promising molecules. Here, we summarize recent knowledge about their role in the regulation of CAF transformation and tumor-promoting functions, highlighting their therapeutic utility and challenges.
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spelling pubmed-73526552020-07-21 Emerging Therapeutic RNAs for the Targeting of Cancer Associated Fibroblasts Santana-Viera, Laura Ibba, Maria L. Rotoli, Deborah Catuogno, Silvia Esposito, Carla L. Cancers (Basel) Review Tumor mass consists of a complex ensemble of malignant cancer cells and a wide variety of resident and infiltrating cells, secreted factors, and extracellular matrix proteins that are referred as tumor microenvironment (TME). Cancer associated fibroblasts (CAFs) are key TME components that support tumor growth, generating a physical barrier against drugs and immune infiltration, and contributing to regulate malignant progression. Thus, it is largely accepted that therapeutic approaches aimed at hampering the interactions between tumor cells and CAFs can enhance the effectiveness of anti-cancer treatments. In this view, nucleic acid therapeutics have emerged as promising molecules. Here, we summarize recent knowledge about their role in the regulation of CAF transformation and tumor-promoting functions, highlighting their therapeutic utility and challenges. MDPI 2020-05-26 /pmc/articles/PMC7352655/ /pubmed/32466591 http://dx.doi.org/10.3390/cancers12061365 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
Santana-Viera, Laura
Ibba, Maria L.
Rotoli, Deborah
Catuogno, Silvia
Esposito, Carla L.
Emerging Therapeutic RNAs for the Targeting of Cancer Associated Fibroblasts
title Emerging Therapeutic RNAs for the Targeting of Cancer Associated Fibroblasts
title_full Emerging Therapeutic RNAs for the Targeting of Cancer Associated Fibroblasts
title_fullStr Emerging Therapeutic RNAs for the Targeting of Cancer Associated Fibroblasts
title_full_unstemmed Emerging Therapeutic RNAs for the Targeting of Cancer Associated Fibroblasts
title_short Emerging Therapeutic RNAs for the Targeting of Cancer Associated Fibroblasts
title_sort emerging therapeutic rnas for the targeting of cancer associated fibroblasts
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7352655/
https://www.ncbi.nlm.nih.gov/pubmed/32466591
http://dx.doi.org/10.3390/cancers12061365
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