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Downregulation of microRNA-29b in cancer and fibrosis: molecular insights and clinical implications

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dc.contributor.author Chitkara, Deepak
dc.date.accessioned 2025-03-03T09:02:48Z
dc.date.available 2025-03-03T09:02:48Z
dc.date.issued 2024-11
dc.identifier.uri https://www.sciencedirect.com/science/article/pii/S1359644624003155
dc.identifier.uri http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/18106
dc.description.abstract MicroRNA-29b (miR-29b) is known for its therapeutic potential as an antifibrotic and anticancer agent. In fibrotic conditions, miR-29b inhibits fibrogenesis by downregulating crucial regulators such as collagens, extracellular matrix proteins and the transforming growth factor-β pathway. Similarly, in cancer, it acts as a tumor suppressor by downregulating various oncogenes and signaling pathways involved in cancer progression, such as Wnt–β-catenin, p38–mitogen-activated protein kinase and nuclear factor-κB. However, the upregulation of these pathways suppresses miR-29b, contributing to fibrosis and cancer development. Preclinical research and clinical trials have shown that delivering exogenous miR-29b mimics can restore its expression, attenuating tumorigenesis and fibrogenesis. This review discusses miR-29b’s potential and its possible therapeutic development for cancer and fibrotic disorders. en_US
dc.language.iso en en_US
dc.publisher Elsevier en_US
dc.subject Pharmacy en_US
dc.subject miR-29b en_US
dc.subject Fibrosis en_US
dc.subject Cancer en_US
dc.subject ECM accumulation en_US
dc.subject TGF-β en_US
dc.subject NF-κB en_US
dc.title Downregulation of microRNA-29b in cancer and fibrosis: molecular insights and clinical implications en_US
dc.type Article en_US


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