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Recent Advances in the Development of TGF-β Signaling Inhibitors for Anticancer Therapy

TGF-β is a multifunctional cytokine that plays an important role in both physiologic and pathologic processes, including cancer. Importantly, TGF-β has a dual role in tumorigenesis, acting as a tumor suppressor or a tumor promoter, depending on the stage of tumor development. The aberrantly upregula...

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Autor principal: Lee, Ho-Jae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Cancer Prevention 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7783242/
https://www.ncbi.nlm.nih.gov/pubmed/33409254
http://dx.doi.org/10.15430/JCP.2020.25.4.213
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author Lee, Ho-Jae
author_facet Lee, Ho-Jae
author_sort Lee, Ho-Jae
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description TGF-β is a multifunctional cytokine that plays an important role in both physiologic and pathologic processes, including cancer. Importantly, TGF-β has a dual role in tumorigenesis, acting as a tumor suppressor or a tumor promoter, depending on the stage of tumor development. The aberrantly upregulated production of TGF-β has been strongly implicated in tumor progression, angiogenesis, and metastasis, as well as immune evasion. Therefore, hyperactivated TGF-β signaling is considered a potential therapeutic target for cancer therapy. Numerous inhibitors of overactivated TGF-β signaling have been developed, and some of them are currently in clinical trials. This review focuses on the TGF-β signaling that contributes to tumor progression and immune evasion in the tumor microenvironment and presents recent achievements on TGF-β signaling inhibition as a single or combined therapeutic approach in cancer therapy.
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spelling pubmed-77832422021-01-05 Recent Advances in the Development of TGF-β Signaling Inhibitors for Anticancer Therapy Lee, Ho-Jae J Cancer Prev Review TGF-β is a multifunctional cytokine that plays an important role in both physiologic and pathologic processes, including cancer. Importantly, TGF-β has a dual role in tumorigenesis, acting as a tumor suppressor or a tumor promoter, depending on the stage of tumor development. The aberrantly upregulated production of TGF-β has been strongly implicated in tumor progression, angiogenesis, and metastasis, as well as immune evasion. Therefore, hyperactivated TGF-β signaling is considered a potential therapeutic target for cancer therapy. Numerous inhibitors of overactivated TGF-β signaling have been developed, and some of them are currently in clinical trials. This review focuses on the TGF-β signaling that contributes to tumor progression and immune evasion in the tumor microenvironment and presents recent achievements on TGF-β signaling inhibition as a single or combined therapeutic approach in cancer therapy. Korean Society of Cancer Prevention 2020-12-30 2020-12-30 /pmc/articles/PMC7783242/ /pubmed/33409254 http://dx.doi.org/10.15430/JCP.2020.25.4.213 Text en Copyright © 2020 Korean Society of Cancer Prevention This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Lee, Ho-Jae
Recent Advances in the Development of TGF-β Signaling Inhibitors for Anticancer Therapy
title Recent Advances in the Development of TGF-β Signaling Inhibitors for Anticancer Therapy
title_full Recent Advances in the Development of TGF-β Signaling Inhibitors for Anticancer Therapy
title_fullStr Recent Advances in the Development of TGF-β Signaling Inhibitors for Anticancer Therapy
title_full_unstemmed Recent Advances in the Development of TGF-β Signaling Inhibitors for Anticancer Therapy
title_short Recent Advances in the Development of TGF-β Signaling Inhibitors for Anticancer Therapy
title_sort recent advances in the development of tgf-β signaling inhibitors for anticancer therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7783242/
https://www.ncbi.nlm.nih.gov/pubmed/33409254
http://dx.doi.org/10.15430/JCP.2020.25.4.213
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