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The Dual Role of Bone Morphogenetic Proteins in Cancer

Bone morphogenetic proteins (BMPs) are a diverse class of molecules with over 20 growth factor proteins that belong to the transforming growth factor-β (TGF-β) family and are highly associated with bone formation and disease development. Aberrant expression of various BMPs has been reported in sever...

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Autores principales: Bach, Duc-Hiep, Park, Hyen Joo, Lee, Sang Kook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5723373/
https://www.ncbi.nlm.nih.gov/pubmed/29234727
http://dx.doi.org/10.1016/j.omto.2017.10.002
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author Bach, Duc-Hiep
Park, Hyen Joo
Lee, Sang Kook
author_facet Bach, Duc-Hiep
Park, Hyen Joo
Lee, Sang Kook
author_sort Bach, Duc-Hiep
collection PubMed
description Bone morphogenetic proteins (BMPs) are a diverse class of molecules with over 20 growth factor proteins that belong to the transforming growth factor-β (TGF-β) family and are highly associated with bone formation and disease development. Aberrant expression of various BMPs has been reported in several cancer tissues. Biological function studies have elicited the dual role of BMPs in both cancer development and suppression. Furthermore, a variety of BMP antagonists, ligands, and receptors have been shown to reduce or enhance tumorigenesis and metastasis. Knockout mouse models of BMP signaling components have also revealed that the suppression of BMP signaling impairs cancer metastasis. Herein, we highlight the basic clinical background and involvement of BMPs in modulating cancer progression and their dynamic interactions (e.g., with microRNAs) in the tumor microenvironment in addition to their mutations and roles in chemoprevention. We also suggest that BMPs should be considered a powerful putative therapeutic target in tumorigenesis and bone metastasis.
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spelling pubmed-57233732017-12-11 The Dual Role of Bone Morphogenetic Proteins in Cancer Bach, Duc-Hiep Park, Hyen Joo Lee, Sang Kook Mol Ther Oncolytics Article Bone morphogenetic proteins (BMPs) are a diverse class of molecules with over 20 growth factor proteins that belong to the transforming growth factor-β (TGF-β) family and are highly associated with bone formation and disease development. Aberrant expression of various BMPs has been reported in several cancer tissues. Biological function studies have elicited the dual role of BMPs in both cancer development and suppression. Furthermore, a variety of BMP antagonists, ligands, and receptors have been shown to reduce or enhance tumorigenesis and metastasis. Knockout mouse models of BMP signaling components have also revealed that the suppression of BMP signaling impairs cancer metastasis. Herein, we highlight the basic clinical background and involvement of BMPs in modulating cancer progression and their dynamic interactions (e.g., with microRNAs) in the tumor microenvironment in addition to their mutations and roles in chemoprevention. We also suggest that BMPs should be considered a powerful putative therapeutic target in tumorigenesis and bone metastasis. American Society of Gene & Cell Therapy 2017-10-24 /pmc/articles/PMC5723373/ /pubmed/29234727 http://dx.doi.org/10.1016/j.omto.2017.10.002 Text en © 2017 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Bach, Duc-Hiep
Park, Hyen Joo
Lee, Sang Kook
The Dual Role of Bone Morphogenetic Proteins in Cancer
title The Dual Role of Bone Morphogenetic Proteins in Cancer
title_full The Dual Role of Bone Morphogenetic Proteins in Cancer
title_fullStr The Dual Role of Bone Morphogenetic Proteins in Cancer
title_full_unstemmed The Dual Role of Bone Morphogenetic Proteins in Cancer
title_short The Dual Role of Bone Morphogenetic Proteins in Cancer
title_sort dual role of bone morphogenetic proteins in cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5723373/
https://www.ncbi.nlm.nih.gov/pubmed/29234727
http://dx.doi.org/10.1016/j.omto.2017.10.002
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