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The TGF-β Pathway: A Pharmacological Target in Hepatocellular Carcinoma?

SIMPLE SUMMARY: Transforming Growth Factor-beta (TGF-β) signaling is crucial to maintain tissue homeostasis. Alterations in TGF-β signaling impact tissue functions and favor the development of diseases, including cancer. In hepatocellular carcinoma (HCC), the most frequent liver tumor, TGF-β plays a...

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Autores principales: Gonzalez-Sanchez, Ester, Vaquero, Javier, Férnandez-Barrena, Maite G., Lasarte, Juan José, Avila, Matías A., Sarobe, Pablo, Reig, María, Calvo, Mariona, Fabregat, Isabel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8268320/
https://www.ncbi.nlm.nih.gov/pubmed/34209646
http://dx.doi.org/10.3390/cancers13133248
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author Gonzalez-Sanchez, Ester
Vaquero, Javier
Férnandez-Barrena, Maite G.
Lasarte, Juan José
Avila, Matías A.
Sarobe, Pablo
Reig, María
Calvo, Mariona
Fabregat, Isabel
author_facet Gonzalez-Sanchez, Ester
Vaquero, Javier
Férnandez-Barrena, Maite G.
Lasarte, Juan José
Avila, Matías A.
Sarobe, Pablo
Reig, María
Calvo, Mariona
Fabregat, Isabel
author_sort Gonzalez-Sanchez, Ester
collection PubMed
description SIMPLE SUMMARY: Transforming Growth Factor-beta (TGF-β) signaling is crucial to maintain tissue homeostasis. Alterations in TGF-β signaling impact tissue functions and favor the development of diseases, including cancer. In hepatocellular carcinoma (HCC), the most frequent liver tumor, TGF-β plays a dual role, acting as a tumor-suppressor at early stages but contributing to tumor progression at late stages. TGF-β can also act on the stroma, favoring progression and driving immune evasion of cancer cells. Therefore, inhibiting the TGF-β pathway may constitute an effective option for HCC treatment. However, its inhibition in the wrong patients could have negative effects. To overcome this obstacle, it is mandatory to identify relevant biomarkers of the status of TGF-β signaling in HCC. In this review we summarize the functions of TGF-β in HCC and the available strategies for targeting TGF-β signaling. We also present the clinical results of the use of TGF-β inhibitors and their future in HCC. ABSTRACT: Transforming Growth Factor-beta (TGF-β) superfamily members are essential for tissue homeostasis and consequently, dysregulation of their signaling pathways contributes to the development of human diseases. In the liver, TGF-β signaling participates in all the stages of disease progression from initial liver injury to hepatocellular carcinoma (HCC). During liver carcinogenesis, TGF-β plays a dual role on the malignant cell, behaving as a suppressor factor at early stages, but contributing to later tumor progression once cells escape from its cytostatic effects. Moreover, TGF-β can modulate the response of the cells forming the tumor microenvironment that may also contribute to HCC progression, and drive immune evasion of cancer cells. Thus, targeting the TGF-β pathway may constitute an effective therapeutic option for HCC treatment. However, it is crucial to identify biomarkers that allow to predict the response of the tumors and appropriately select the patients that could benefit from TGF-β inhibitory therapies. Here we review the functions of TGF-β on HCC malignant and tumor microenvironment cells, and the current strategies targeting TGF-β signaling for cancer therapy. We also summarize the clinical impact of TGF-β inhibitors in HCC patients and provide a perspective on its future use alone or in combinatorial strategies for HCC treatment.
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spelling pubmed-82683202021-07-10 The TGF-β Pathway: A Pharmacological Target in Hepatocellular Carcinoma? Gonzalez-Sanchez, Ester Vaquero, Javier Férnandez-Barrena, Maite G. Lasarte, Juan José Avila, Matías A. Sarobe, Pablo Reig, María Calvo, Mariona Fabregat, Isabel Cancers (Basel) Review SIMPLE SUMMARY: Transforming Growth Factor-beta (TGF-β) signaling is crucial to maintain tissue homeostasis. Alterations in TGF-β signaling impact tissue functions and favor the development of diseases, including cancer. In hepatocellular carcinoma (HCC), the most frequent liver tumor, TGF-β plays a dual role, acting as a tumor-suppressor at early stages but contributing to tumor progression at late stages. TGF-β can also act on the stroma, favoring progression and driving immune evasion of cancer cells. Therefore, inhibiting the TGF-β pathway may constitute an effective option for HCC treatment. However, its inhibition in the wrong patients could have negative effects. To overcome this obstacle, it is mandatory to identify relevant biomarkers of the status of TGF-β signaling in HCC. In this review we summarize the functions of TGF-β in HCC and the available strategies for targeting TGF-β signaling. We also present the clinical results of the use of TGF-β inhibitors and their future in HCC. ABSTRACT: Transforming Growth Factor-beta (TGF-β) superfamily members are essential for tissue homeostasis and consequently, dysregulation of their signaling pathways contributes to the development of human diseases. In the liver, TGF-β signaling participates in all the stages of disease progression from initial liver injury to hepatocellular carcinoma (HCC). During liver carcinogenesis, TGF-β plays a dual role on the malignant cell, behaving as a suppressor factor at early stages, but contributing to later tumor progression once cells escape from its cytostatic effects. Moreover, TGF-β can modulate the response of the cells forming the tumor microenvironment that may also contribute to HCC progression, and drive immune evasion of cancer cells. Thus, targeting the TGF-β pathway may constitute an effective therapeutic option for HCC treatment. However, it is crucial to identify biomarkers that allow to predict the response of the tumors and appropriately select the patients that could benefit from TGF-β inhibitory therapies. Here we review the functions of TGF-β on HCC malignant and tumor microenvironment cells, and the current strategies targeting TGF-β signaling for cancer therapy. We also summarize the clinical impact of TGF-β inhibitors in HCC patients and provide a perspective on its future use alone or in combinatorial strategies for HCC treatment. MDPI 2021-06-29 /pmc/articles/PMC8268320/ /pubmed/34209646 http://dx.doi.org/10.3390/cancers13133248 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Gonzalez-Sanchez, Ester
Vaquero, Javier
Férnandez-Barrena, Maite G.
Lasarte, Juan José
Avila, Matías A.
Sarobe, Pablo
Reig, María
Calvo, Mariona
Fabregat, Isabel
The TGF-β Pathway: A Pharmacological Target in Hepatocellular Carcinoma?
title The TGF-β Pathway: A Pharmacological Target in Hepatocellular Carcinoma?
title_full The TGF-β Pathway: A Pharmacological Target in Hepatocellular Carcinoma?
title_fullStr The TGF-β Pathway: A Pharmacological Target in Hepatocellular Carcinoma?
title_full_unstemmed The TGF-β Pathway: A Pharmacological Target in Hepatocellular Carcinoma?
title_short The TGF-β Pathway: A Pharmacological Target in Hepatocellular Carcinoma?
title_sort tgf-β pathway: a pharmacological target in hepatocellular carcinoma?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8268320/
https://www.ncbi.nlm.nih.gov/pubmed/34209646
http://dx.doi.org/10.3390/cancers13133248
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