The potential of miR-29 in modulating tumor angiogenesis: a comprehensive review

Abstract MicroRNAs (miRNAs) are a class of short non-coding RNAs that play a crucial role in the post-transcriptional regulation of gene expression. They are associated with various biological processes related to tumors. Among the numerous miRNAs, miR-29 has garnered attention for its role in regul...

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Main Authors: Rui-Ting Zhou, Xiao-Jie Luo, Xiao-Xin-Ran Zhang, Jiang-Feng Wu, Yi-Ran Ni
Format: Article
Language:English
Published: Springer 2025-04-01
Series:Discover Oncology
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Online Access:https://doi.org/10.1007/s12672-025-02246-3
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author Rui-Ting Zhou
Xiao-Jie Luo
Xiao-Xin-Ran Zhang
Jiang-Feng Wu
Yi-Ran Ni
author_facet Rui-Ting Zhou
Xiao-Jie Luo
Xiao-Xin-Ran Zhang
Jiang-Feng Wu
Yi-Ran Ni
author_sort Rui-Ting Zhou
collection DOAJ
description Abstract MicroRNAs (miRNAs) are a class of short non-coding RNAs that play a crucial role in the post-transcriptional regulation of gene expression. They are associated with various biological processes related to tumors. Among the numerous miRNAs, miR-29 has garnered attention for its role in regulating tumor angiogenesis. In numerous human tumors, miR-29 has been demonstrated to negatively correlate with the capacity for angiogenesis and the degree of malignancy, as well as with the expression levels of pro-angiogenic factors such as vascular endothelial growth factor vascular endothelial growth factor (VEGF), platelet-derived growth factor (PDGF), and matrix metalloproteinase (MMP)-2. Multiple studies, utilizing techniques like dual-luciferase reporter assays, have confirmed that miR-29 directly targets the 3'-untranslated region (UTR) of mRNAs for VEGF, PDGF, and MMP-2. Extensive investigations involving tumor cell lines and animal models have shown that the overexpression of miR-29, achieved through miRNA transfection or the introduction of miRNA mimics, effectively inhibits angiogenesis by upregulating these pro-angiogenic factors. Conversely, downregulation of miR-29 using specific inhibitors promotes angiogenesis. While small molecule inhibitors and antibodies targeting VEGF constitute a primary strategy in anti-angiogenesis therapies, miR-29's ability to target multiple pro-angiogenic molecules positions it as a promising candidate for future therapeutic interventions, especially with ongoing advancements in nucleic acid drug design and delivery systems.
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spelling doaj-art-831cfe94c26d4ddeaa0361e57763a6f32025-08-20T03:10:07ZengSpringerDiscover Oncology2730-60112025-04-0116111110.1007/s12672-025-02246-3The potential of miR-29 in modulating tumor angiogenesis: a comprehensive reviewRui-Ting Zhou0Xiao-Jie Luo1Xiao-Xin-Ran Zhang2Jiang-Feng Wu3Yi-Ran Ni4Hubei Key Laboratory of Tumor Microenvironment and Immunotherapy, China Three Gorges UniversityHubei Key Laboratory of Tumor Microenvironment and Immunotherapy, China Three Gorges UniversityHubei Key Laboratory of Tumor Microenvironment and Immunotherapy, China Three Gorges UniversityHubei Key Laboratory of Tumor Microenvironment and Immunotherapy, China Three Gorges UniversityHubei Key Laboratory of Tumor Microenvironment and Immunotherapy, China Three Gorges UniversityAbstract MicroRNAs (miRNAs) are a class of short non-coding RNAs that play a crucial role in the post-transcriptional regulation of gene expression. They are associated with various biological processes related to tumors. Among the numerous miRNAs, miR-29 has garnered attention for its role in regulating tumor angiogenesis. In numerous human tumors, miR-29 has been demonstrated to negatively correlate with the capacity for angiogenesis and the degree of malignancy, as well as with the expression levels of pro-angiogenic factors such as vascular endothelial growth factor vascular endothelial growth factor (VEGF), platelet-derived growth factor (PDGF), and matrix metalloproteinase (MMP)-2. Multiple studies, utilizing techniques like dual-luciferase reporter assays, have confirmed that miR-29 directly targets the 3'-untranslated region (UTR) of mRNAs for VEGF, PDGF, and MMP-2. Extensive investigations involving tumor cell lines and animal models have shown that the overexpression of miR-29, achieved through miRNA transfection or the introduction of miRNA mimics, effectively inhibits angiogenesis by upregulating these pro-angiogenic factors. Conversely, downregulation of miR-29 using specific inhibitors promotes angiogenesis. While small molecule inhibitors and antibodies targeting VEGF constitute a primary strategy in anti-angiogenesis therapies, miR-29's ability to target multiple pro-angiogenic molecules positions it as a promising candidate for future therapeutic interventions, especially with ongoing advancements in nucleic acid drug design and delivery systems.https://doi.org/10.1007/s12672-025-02246-3AngiogenesismiR-29Vascular endothelial growth factorClinical application
spellingShingle Rui-Ting Zhou
Xiao-Jie Luo
Xiao-Xin-Ran Zhang
Jiang-Feng Wu
Yi-Ran Ni
The potential of miR-29 in modulating tumor angiogenesis: a comprehensive review
Discover Oncology
Angiogenesis
miR-29
Vascular endothelial growth factor
Clinical application
title The potential of miR-29 in modulating tumor angiogenesis: a comprehensive review
title_full The potential of miR-29 in modulating tumor angiogenesis: a comprehensive review
title_fullStr The potential of miR-29 in modulating tumor angiogenesis: a comprehensive review
title_full_unstemmed The potential of miR-29 in modulating tumor angiogenesis: a comprehensive review
title_short The potential of miR-29 in modulating tumor angiogenesis: a comprehensive review
title_sort potential of mir 29 in modulating tumor angiogenesis a comprehensive review
topic Angiogenesis
miR-29
Vascular endothelial growth factor
Clinical application
url https://doi.org/10.1007/s12672-025-02246-3
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