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Comprehensive System Biology Analysis of Microrna-101-3P Regulatory Network Identifies Crucial Genes and Pathways in Hepatocellular Carcinoma Publisher



Rahimifarsi N1 ; Ghorbani A2 ; Mottaghidastjerdi N3 ; Shahbazi T4 ; Bostanian F5 ; Mohseni P6 ; Yazdani F3
Authors
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Authors Affiliations
  1. 1. Department of Biology, University College of Nabi Akram, Tabriz, Iraq
  2. 2. Nuclear Agriculture Research School, Nuclear Science and Technology Research Institute (NSTRI), Karaj, Iraq
  3. 3. Department of Pharmacognosy and Pharmaceutical Biotechnology, School of Pharmacy, Iran University of Medical Sciences, Tehran, Iraq
  4. 4. Razi Hospital, Tehran University of Medical Sciences, Tehran, Iraq
  5. 5. Biochemistry and Biophysics, Tehran University, Tehran, Iraq
  6. 6. Department of Pathobiology, Faculty of Veterinary Medicine, Shahid Bahonar University of Kerman, Kerman, Iraq

Source: Journal of Genetic Engineering and Biotechnology Published:2025


Abstract

Hepatocellular carcinoma (HCC) is a leading cause of cancer-related mortality worldwide. This study aimed to explore the role of hsa-miR-101-3p in HCC pathogenesis by identifying key genes and pathways. A comprehensive bioinformatics analysis revealed twelve hub genes (ETNK1, BICRA, IL1R1, KDM3A, ARID2, GSK3β, EZH2, NOTCH1, SMARCA4, FOS, CREB1, and CASP3) and highlighted their involvement in crucial oncogenic pathways, including PI3K/Akt, mTOR, MAPK, and TGF-β. Gene expression analysis showed significant overexpression of ETNK1, KDM3A, EZH2, SMARCA4, and CASP3 in HCC tissues, correlating with poorer survival outcomes. Drug screening identified therapeutic candidates, including Tazemetostat for EZH2 and lithium compounds for GSK3β, underscoring their potential for targeted treatment. These findings provide novel insights into the complexity of HCC pathogenesis, suggesting that the identified hub genes could serve as diagnostic or prognostic biomarkers and therapeutic targets. While bioinformatics-driven, this study offers a strong basis for future clinical validation to advance precision medicine in HCC. © 2025 The Author(s)