Related Experiment Video
Updated: Mar 2, 2026

An In Vitro Protocol for Evaluating MicroRNA Levels, Functions, and Associated Target Genes in Tumor Cells
Published on: May 21, 2019
MicroRNA-195 inhibits human gastric cancer by directly targeting basic fibroblast growth factor
1Department of General Surgery, The First Affiliated Hospital of Anhui Medical University, 218 Jixi Road, Hefei, 230032, Anhui, China.
Purpose:
Gastric cancer (GC) is one of the fatal malignancies worldwide with high occurrences but poor outcomes. bFGF has been shown to play significant roles in GC. Yet, whether bFGF affects the development of GC is less studied.
Methods:
MicroRNA assays, real-time PCR, and western blot were conducted for expression analysis of miR-195-5p and basic fibroblast growth factor (bFGF). Luciferase activity was measured with mutated bFGF 3'-UTR sequence at the 3' end of the luciferase gene. Two GC cell lines, SNU-1 and KATO-3 overexpressing miR-195-5p and bFGF were subjected to wound healing assay and transwell invasion assay. Mouse GC xenograft model was established and subjected to tumor size analysis.
Results:
Expression levels of miR-195-5p and bFGF showed negative correlation in human GC tissues. MiR-195-5p directly targeted bFGF 3'-UTR as demonstrated by luciferase activity assay. MiR-195-5p, through downregulating bFGF, inhibited the migration and invasion of SNU-1 and KATO-3 cells, as well as tumorigenesis in a xenograft mouse model, which could be restored by re-introduction of bFGF.
Conclusions:
MiR-195-5p inhibits tumorigenesis of GC through suppressing bFGF, which supports both miR-195-5p and bFGF as potential therapeutic targets in the treatment of GC.
Insights
MicroRNA-195-5p suppresses gastric cancer (GC) development by targeting basic fibroblast growth factor (bFGF). This finding highlights miR-195-5p and bFGF as potential therapeutic targets for GC treatment.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Gastric cancer (GC) is a leading cause of cancer mortality globally.
- Basic fibroblast growth factor (bFGF) is implicated in GC progression, but its regulatory mechanisms are not fully understood.
Purpose of the Study:
- To investigate the role of miR-195-5p in gastric cancer.
- To elucidate the relationship between miR-195-5p and bFGF in GC development.
Main Methods:
- Expression analysis of miR-195-5p and bFGF using real-time PCR and western blot.
- Luciferase activity assays to confirm direct targeting of bFGF by miR-195-5p.
- In vitro (cell migration and invasion assays) and in vivo (xenograft mouse model) experiments to assess the functional impact of miR-195-5p and bFGF.
Main Results:
- A negative correlation was observed between miR-195-5p and bFGF expression in human GC tissues.
- MiR-195-5p directly targets the 3'-UTR of bFGF, leading to its downregulation.
- Downregulation of bFGF by miR-195-5p inhibited GC cell migration, invasion, and tumorigenesis in vivo, effects that were reversible upon bFGF reintroduction.
Conclusions:
- MiR-195-5p exerts tumor-suppressive effects in gastric cancer by inhibiting bFGF.
- Both miR-195-5p and bFGF represent promising therapeutic targets for gastric cancer treatment.
Related Concept Videos
MicroRNAs
MicroRNAs
Mitogens and the Cell Cycle
mTOR Signaling and Cancer Progression
The mTOR pathway or the...
Targeted Cancer Therapies
There are several types of targeted therapies against...
Abnormal Proliferation

