Research Paper Advance Articles
Deregulated miR-145 and miR-27b in hutchinson-gilford progeria syndrome: implications for adipogenesis
- 1 Epigenetics of Aging, Department of Dermatology and Allergy, TUM School of Medicine, Munich Institute of Biomedical Engineering (MIBE), Technical University of Munich (TUM), Garching 85748, Germany
Received: May 9, 2025 Accepted: August 6, 2025 Published: August 27, 2025
https://doi.org/10.18632/aging.206309How to Cite
Copyright: © 2025 Fenzl et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Abstract
Hutchinson-Gilford progeria syndrome (HGPS) is a rare and fatal disorder that causes premature aging, affecting approximately one in 4–8 million births. Most cases result from a mutation in the lamin A/C (LMNA) gene, leading to the production of progerin, an aberrant lamin A variant that disrupts nuclear architecture and alters gene expression, including microRNA (miRNA) deregulation. This study aimed to investigate the molecular mechanisms underlying HGPS and aging using global miRNA sequencing to identify key deregulated miRNAs. Both miR-145 and miR-27b were significantly altered in HGPS. Functional experiments further revealed their crucial role in adipogenesis. Downregulation of these miRNAs in HGPS cells enhanced adipocyte differentiation, whereas their upregulation in control cells suppressed this process. These findings indicate that elevated levels of miR-145-5p and miR-27b-3p impair adipogenesis, providing mechanistic insights into HGPS pathophysiology and highlight new potential therapeutic avenues for both HGPS and metabolic disorders.