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RUNX Family in Hypoxic Microenvironment and Angiogenesis in Cancers

The tumor microenvironment (TME) is broadly implicated in tumorigenesis, as tumor cells interact with surrounding cells to influence the development and progression of the tumor. Blood vessels are a major component of the TME and are attributed to the creation of a hypoxic microenvironment, which is...

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Detalles Bibliográficos
Autor principal: Lee, You Mie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9564080/
https://www.ncbi.nlm.nih.gov/pubmed/36231060
http://dx.doi.org/10.3390/cells11193098
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author Lee, You Mie
author_facet Lee, You Mie
author_sort Lee, You Mie
collection PubMed
description The tumor microenvironment (TME) is broadly implicated in tumorigenesis, as tumor cells interact with surrounding cells to influence the development and progression of the tumor. Blood vessels are a major component of the TME and are attributed to the creation of a hypoxic microenvironment, which is a common feature of advanced cancers and inflamed premalignant tissues. Runt-related transcription factor (RUNX) proteins, a transcription factor family of developmental master regulators, are involved in vital cellular processes such as differentiation, proliferation, cell lineage specification, and apoptosis. Furthermore, the RUNX family is involved in the regulation of various oncogenic processes and signaling pathways as well as tumor suppressive functions, suggesting that the RUNX family plays a strategic role in tumorigenesis. In this review, we have discussed the relevant findings that describe the crosstalk of the RUNX family with the hypoxic TME and tumor angiogenesis or with their signaling molecules in cancer development and progression.
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spelling pubmed-95640802022-10-15 RUNX Family in Hypoxic Microenvironment and Angiogenesis in Cancers Lee, You Mie Cells Review The tumor microenvironment (TME) is broadly implicated in tumorigenesis, as tumor cells interact with surrounding cells to influence the development and progression of the tumor. Blood vessels are a major component of the TME and are attributed to the creation of a hypoxic microenvironment, which is a common feature of advanced cancers and inflamed premalignant tissues. Runt-related transcription factor (RUNX) proteins, a transcription factor family of developmental master regulators, are involved in vital cellular processes such as differentiation, proliferation, cell lineage specification, and apoptosis. Furthermore, the RUNX family is involved in the regulation of various oncogenic processes and signaling pathways as well as tumor suppressive functions, suggesting that the RUNX family plays a strategic role in tumorigenesis. In this review, we have discussed the relevant findings that describe the crosstalk of the RUNX family with the hypoxic TME and tumor angiogenesis or with their signaling molecules in cancer development and progression. MDPI 2022-10-01 /pmc/articles/PMC9564080/ /pubmed/36231060 http://dx.doi.org/10.3390/cells11193098 Text en © 2022 by the author. 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
Lee, You Mie
RUNX Family in Hypoxic Microenvironment and Angiogenesis in Cancers
title RUNX Family in Hypoxic Microenvironment and Angiogenesis in Cancers
title_full RUNX Family in Hypoxic Microenvironment and Angiogenesis in Cancers
title_fullStr RUNX Family in Hypoxic Microenvironment and Angiogenesis in Cancers
title_full_unstemmed RUNX Family in Hypoxic Microenvironment and Angiogenesis in Cancers
title_short RUNX Family in Hypoxic Microenvironment and Angiogenesis in Cancers
title_sort runx family in hypoxic microenvironment and angiogenesis in cancers
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9564080/
https://www.ncbi.nlm.nih.gov/pubmed/36231060
http://dx.doi.org/10.3390/cells11193098
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