Proteomic profiling identifies miR-423-5p as a modulator of oncogenic metabolism in HCC

miR-423-5p acts as a tumor suppressor in HCC by targeting key nodes of pro-tumorigenic signalling. miR-423-5p significantly altered metabolic pathways, including purine/pyrimidine metabolism and gluconeogenesis. Seven miR-423-5p targets correlate with poor prognosis in TCGA-LIHC patients and are downregulated in miR-423-5p overexpressing HCC cells. miR-423-5p over-expression induces a significant downregulation of MCM7, DVL3, IMPDH1, SPEE in HCC cell models. miR-423-5p limits tumor metabolic plasticity, suggesting therapeutic potential.

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Publication Details

Journal
Journal of Translational Medicine
Published
2025-09-24
DOI
https://doi.org/10.1186/s12967-025-07039-4
Primary Topic
RNA modifications and cancer
Type
article
Field-Weighted Citation Impact
0.00

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article

Proteomic profiling identifies miR-423-5p as a modulator of oncogenic metabolism in HCC

Elisabetta A. M. Verderio, Madhura S. Tathode, Rossella Sperlongano, Amalia Luce et al.
Journal of Translational Medicine
RNA modifications and cancer
article

Proteomic profiling identifies miR-423-5p as a modulator of oncogenic metabolism in HCC

Elisabetta A. M. Verderio, Madhura S. Tathode, Rossella Sperlongano, Amalia Luce, Luigi Mele, Gabriella Misso, Silvia Zappavigna, David J. Boocock, Maria Preziosa Romano, Michele Caraglia, Ines Simeone, Marco Bocchetti, Clare Coveney, Alessia Maria Cossu, Giovanni Vitale, Maria Roberta De Iesu
article en

Abstract

miR-423-5p acts as a tumor suppressor in HCC by targeting key nodes of pro-tumorigenic signalling. miR-423-5p significantly altered metabolic pathways, including purine/pyrimidine metabolism and gluconeogenesis. Seven miR-423-5p targets correlate with poor prognosis in TCGA-LIHC patients and are downregulated in miR-423-5p overexpressing HCC cells. miR-423-5p over-expression induces a significant downregulation of MCM7, DVL3, IMPDH1, SPEE in HCC cell models. miR-423-5p limits tumor metabolic plasticity, suggesting therapeutic potential.

Journal of Translational MedicineVol. 23(1)
University of Sannio (IT), University of Milan (IT), University of Campania "Luigi Vanvitelli" (IT), University of Basilicata (IT), Biogem (IT), University of Campania "Luigi Vanvitelli" (IT), IRCCS Istituto Auxologico Italiano (IT), Istituti di Ricovero e Cura a Carattere Scientifico (IT), IRCCS Humanitas Research Hospital (IT), Link Campus University (IT), Nottingham Trent University (GB), University of Bologna (IT)
National Eye Institute
Openalex Percentile: Top 77%
RNA modifications and cancer
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