Related Experiment Video
Updated: Oct 4, 2025

An In Vitro Protocol for Evaluating MicroRNA Levels, Functions, and Associated Target Genes in Tumor Cells
Published on: May 21, 2019
Metformin up-regulated miR-107 expression and enhanced the inhibitory effect of miR-107 on gastric cancer growth
Yongyi Chen1,2,3, Wangang Gong1,2,3, Yun Zhou1,2,3
1Institute of Cancer Research and Basic Medical Sciences of Chinese Academy of Sciences, Hangzhou 310022, China.
Abstract:
Gastric cancer (GC) is one of the most common malignant neoplasms and is the third leading cause of cancer-related death around the world. Metformin has been well reported to have an inhibitory effect on the growth of various cancers by regulating the expression of microRNAs (miRNAs). However, the specific miRNA(s) regulated by metformin in GC have not been identified. In this study, real-time reverse transcription polymerase chain reaction (RT-PCR) analysis in vitro indicated that miR-107 expression was up-regulated in metformin-treated SGC-7901 cells compared with untreated SGC-7901 and MGC803 cells. Amplification of miR-107 expression further reduced cell proliferation in metformin-treated GC cells. A bioinformatics analysis showed that mitogen-activated protein kinase 8 (MAPK8) was the common target of metformin and miR-107. MAPK8 expression is associated with immune cell infiltration in GC as well as overall GC patient survival. Our study demonstrates that miR-107 enhances the anti-cancer effects of metformin in GC tissues, which offers a novel strategy for the treatment of GC.
Insights
Metformin enhances anti-cancer effects in gastric cancer (GC) by up-regulating miR-107. This microRNA (miRNA) targets MAPK8, offering a new therapeutic strategy for GC treatment.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Gastric cancer (GC) is a leading cause of cancer-related death globally.
- Metformin shows anti-cancer properties by regulating microRNAs (miRNAs).
- The specific miRNAs influenced by metformin in GC remain largely unidentified.
Purpose of the Study:
- To identify microRNAs regulated by metformin in gastric cancer cells.
- To investigate the role of miR-107 in metformin's anti-cancer effects on GC.
- To explore the molecular mechanisms linking metformin, miR-107, and GC progression.
Main Methods:
- In vitro cell culture using SGC-7901 and MGC803 gastric cancer cell lines.
- Real-time reverse transcription polymerase chain reaction (RT-PCR) to quantify miR-107 expression.
- Bioinformatics analysis to identify potential molecular targets of metformin and miR-107.
Main Results:
- Metformin treatment significantly up-regulated miR-107 expression in GC cells.
- Increased miR-107 expression further inhibited cell proliferation in metformin-treated GC cells.
- Mitogen-activated protein kinase 8 (MAPK8) was identified as a common target of metformin and miR-107, with its expression linked to GC patient survival and immune cell infiltration.
Conclusions:
- miR-107 plays a crucial role in mediating the anti-cancer effects of metformin in gastric cancer.
- The miR-107/MAPK8 pathway represents a novel therapeutic target for gastric cancer.
- This study provides a new strategy for enhancing metformin-based treatments for GC.
Related Concept Videos
MicroRNAs
Oral Hypoglycemic Agents: Biguanides and Glitazones
mTOR Signaling and Cancer Progression
The mTOR pathway or the...
Mitogens and the Cell Cycle
Abnormal Proliferation

