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Updated: Nov 13, 2025

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
Targeting miR-148b-5p Inhibits Immunity Microenvironment and Gastric Cancer Progression
Yuyu Zhang1, Wei Huo1, Lidi Sun1
1Department of Radiation Oncology, The First Hospital of Jilin University, Changchun, China.
Background:
MicroRNAs (miRNAs) have been discovered to dictate the development of various tumors. However, studies on the roles of miRNAs in the progression of gastric cancer (GC) are still lacking.
Methods:
Herein, by analyzing GC cell lines and patients samples, we observed that miR-148b-5p was significantly downregulated in GC. We also confirmed that miR-148b-5p overexpression significantly inhibited GC cell proliferation and invasion in vitro and in vivo.
Results:
Overexpression of miR-148b-5p not only reprogrammed the metabolic properties of GC but also regulated the immune microenvironment by shifting lymphocyte and myeloid populations. Mechanistically, ATPIF1, an important glycolysis-associated gene, was identified as a direct target of miR-148b-5p and mediated the effect of miR-148b-5p. Notably, the low level of miR-148b-5p was significantly related with poor prognosis of GC patients (P < 0.001). Importantly, the levels of miR-148b-5p significantly changed the sensitivity of GC cells to several anti-cancer drugs (Doxorubicin, P < 0.05, Paclitaxel, P < 0.01, Docetaxel, P < 0.05).
Conclusions:
Targeting miR-148b-5p inhibits immunity microenvironment and gastric cancer progression.
Insights
MicroRNA-148b-5p (miR-148b-5p) is downregulated in gastric cancer (GC), inhibiting tumor progression and affecting drug sensitivity. Restoring miR-148b-5p levels shows potential for GC treatment.
Area of Science:
- Oncology
- Molecular Biology
- Immunology
Background:
- MicroRNAs (miRNAs) play critical roles in tumor development.
- Limited research exists on miRNA involvement in gastric cancer (GC) progression.
Purpose of the Study:
- Investigate the role of miR-148b-5p in gastric cancer (GC) development.
- Determine if miR-148b-5p can be a therapeutic target for GC.
Main Methods:
- Analyzed GC cell lines and patient samples to assess miR-148b-5p levels.
- Performed in vitro and in vivo experiments to evaluate the effects of miR-148b-5p overexpression on GC.
- Identified direct targets of miR-148b-5p using mechanistic studies.
Main Results:
- miR-148b-5p was significantly downregulated in GC.
- Overexpression of miR-148b-5p inhibited GC cell proliferation and invasion.
- miR-148b-5p reprogrammed GC metabolism and modulated the immune microenvironment.
- ATPIF1 was identified as a direct target of miR-148b-5p.
- Low miR-148b-5p levels correlated with poor GC patient prognosis and altered sensitivity to anti-cancer drugs.
Conclusions:
- miR-148b-5p acts as a tumor suppressor in GC.
- Targeting miR-148b-5p may offer a novel therapeutic strategy for GC by modulating the immune microenvironment and inhibiting tumor progression.
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