MiR-106b-5p promotes gastric cancer progression by directly targeting the tumor suppressor RBL2

Gastric cancer (GC) is the fifth most common malignancy and the fifth highest cause of cancer-related deaths on a global scale. This study reveals that miR-106b-5p promotes malignant phenotypes in GC by targeting retinoblastoma-like protein 2 (RBL2). Using miR-106b-5p mimic/inhibitor and RBL2 overexpression plasmids in AGS/HGC-27 cells, this study demonstrates that miR-106b-5p promotes proliferation (CCK-8/clone formation) and migration/invasion (Transwell assay) and suppresses apoptosis (flow cytometry), while RBL2 rescues these effects. Luciferase assays confirm that miR-106b-5p directly binds the 3’UTR of RBL2 and western blotting demonstrates the presence of RBL2 downregulation. Animal studies further validate the tumour-promoting role of miR-106b-5p via RBL2 suppression, which suggests its therapeutic potential.

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Publication Details

Journal
Scientific Reports
Published
2025-11-29
DOI
https://doi.org/10.1038/s41598-025-30601-5
Primary Topic
Retinoids in leukemia and cellular processes
Type
article
Field-Weighted Citation Impact
0.00
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article

MiR-106b-5p promotes gastric cancer progression by directly targeting the tumor suppressor RBL2

Biyun Zhang, Yuqing Niu, H. Zhang, Chen Luo et al.
Scientific Reports
Retinoids in leukemia and cellular processes
article

MiR-106b-5p promotes gastric cancer progression by directly targeting the tumor suppressor RBL2

Biyun Zhang, Yuqing Niu, H. Zhang, Chen Luo, Chunyan Wang, Feng Li, T.-Q. Chang
article en

Abstract

Gastric cancer (GC) is the fifth most common malignancy and the fifth highest cause of cancer-related deaths on a global scale. This study reveals that miR-106b-5p promotes malignant phenotypes in GC by targeting retinoblastoma-like protein 2 (RBL2). Using miR-106b-5p mimic/inhibitor and RBL2 overexpression plasmids in AGS/HGC-27 cells, this study demonstrates that miR-106b-5p promotes proliferation (CCK-8/clone formation) and migration/invasion (Transwell assay) and suppresses apoptosis (flow cytometry), while RBL2 rescues these effects. Luciferase assays confirm that miR-106b-5p directly binds the 3’UTR of RBL2 and western blotting demonstrates the presence of RBL2 downregulation. Animal studies further validate the tumour-promoting role of miR-106b-5p via RBL2 suppression, which suggests its therapeutic potential.

Scientific ReportsVol. 16(1)
Shanxi Medical University (CN), Maternal and Child Health Hospital of Xinjiang Uygur Autonomous Region (CN), Shanxi Provincial Cancer Hospital (CN), Shanxi University of Traditional Chinese Medicine (CN)
Openalex Percentile: Top 66%
Retinoids in leukemia and cellular processes
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