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Bone Morphogenetic Protein Signaling in Cancer; Some Topics in the Recent 10 Years

Journal

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fcell.2022.883523

Keywords

BMPs; ALKs; Smads; cancer; metastasis; angiogeneis

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Bone morphogenetic proteins (BMPs), members of the transforming growth factor-beta (TGF-beta) family, are multifunctional cytokines that play a dual role in cancer, acting as both tumor promoters and suppressors. They regulate cancer cell proliferation, malignant phenotypes, and angiogenesis in the tumor microenvironment.
Bone morphogenetic proteins (BMPs), members of the transforming growth factor-beta (TGF-beta) family, are multifunctional cytokines. BMPs have a broad range of functions, and abnormalities in BMP signaling pathways are involved in cancer progression. BMPs activate the proliferation of certain cancer cells. Malignant phenotypes of cancer cells, such as increased motility, invasiveness, and stemness, are enhanced by BMPs. Simultaneously, BMPs act on various cellular components and regulate angiogenesis in the tumor microenvironment. Thus, BMPs function as pro-tumorigenic factors in various types of cancer. However, similar to TGF-beta, which shows both positive and negative effects on tumorigenesis, BMPs also act as tumor suppressors in other types of cancers. In this article, we review important findings published in the recent decade and summarize the pro-oncogenic functions of BMPs and their underlying mechanisms. The current status of BMP-targeted therapies for cancers is also discussed.

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