{"title":"MicroRNA-126: A key regulator of angiogenesis, inflammation, and tumorigenesis — Exploring its multifaceted functions in vascular health and cancer","authors":"Oliwia Woźniak , Bartosz Mierzejewski , Edyta Brzoska","doi":"10.1016/j.bbadis.2025.167984","DOIUrl":null,"url":null,"abstract":"<div><div>MicroRNAs (miRNAs) are small, noncoding RNA molecules (20 to 24 nucleotides) that serve as essential regulators of gene expression through post-transcriptional mechanisms. Among these miRNAs, microRNA-126 (miR-126) has emerged as a key player in angiogenesis, vascular biology, inflammation, and fibrosis. Encoded in the intron of the epidermal growth factor-like domain 7 <em>(EGFL7</em>) gene, miR-126 undergoes canonical biogenesis and forms complexes that repress target messenger RNAs (mRNAs) by binding to complementary sequences in their 3′-untranslated regions (UTRs). MiR-126 have two distinct mature subtypes, namely miR-126-3p and miR-126-5p. The key miR-126 targets include factors such as <em>SPRED1, PIK3R2, PTEN, VEGF, EGFL7, CXCL12,</em> and others. Importantly, changes in miR-126 expression are associated with numerous diseases affecting vascular functions, which highlights its therapeutic potential to improve neovascularisation and underlines its importance as a biomarker for assessing disease risk. This review integrates the current understanding of miR-126 mechanisms of action, its implications in vascular pathologies, and therapeutic strategies, highlighting its importance in cardiovascular health and cancer biology.</div></div>","PeriodicalId":8821,"journal":{"name":"Biochimica et biophysica acta. Molecular basis of disease","volume":"1871 8","pages":"Article 167984"},"PeriodicalIF":4.2000,"publicationDate":"2025-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biochimica et biophysica acta. Molecular basis of disease","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0925443925003321","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
MicroRNAs (miRNAs) are small, noncoding RNA molecules (20 to 24 nucleotides) that serve as essential regulators of gene expression through post-transcriptional mechanisms. Among these miRNAs, microRNA-126 (miR-126) has emerged as a key player in angiogenesis, vascular biology, inflammation, and fibrosis. Encoded in the intron of the epidermal growth factor-like domain 7 (EGFL7) gene, miR-126 undergoes canonical biogenesis and forms complexes that repress target messenger RNAs (mRNAs) by binding to complementary sequences in their 3′-untranslated regions (UTRs). MiR-126 have two distinct mature subtypes, namely miR-126-3p and miR-126-5p. The key miR-126 targets include factors such as SPRED1, PIK3R2, PTEN, VEGF, EGFL7, CXCL12, and others. Importantly, changes in miR-126 expression are associated with numerous diseases affecting vascular functions, which highlights its therapeutic potential to improve neovascularisation and underlines its importance as a biomarker for assessing disease risk. This review integrates the current understanding of miR-126 mechanisms of action, its implications in vascular pathologies, and therapeutic strategies, highlighting its importance in cardiovascular health and cancer biology.
期刊介绍:
BBA Molecular Basis of Disease addresses the biochemistry and molecular genetics of disease processes and models of human disease. This journal covers aspects of aging, cancer, metabolic-, neurological-, and immunological-based disease. Manuscripts focused on using animal models to elucidate biochemical and mechanistic insight in each of these conditions, are particularly encouraged. Manuscripts should emphasize the underlying mechanisms of disease pathways and provide novel contributions to the understanding and/or treatment of these disorders. Highly descriptive and method development submissions may be declined without full review. The submission of uninvited reviews to BBA - Molecular Basis of Disease is strongly discouraged, and any such uninvited review should be accompanied by a coverletter outlining the compelling reasons why the review should be considered.