Related Experiment Video
Updated: Apr 26, 2026

Studying TGF-β Signaling and TGF-β-induced Epithelial-to-mesenchymal Transition in Breast Cancer and Normal Cells
Published on: October 27, 2020
miR-129-1-3p promote BGC-823 cell proliferation by targeting PDCD2
Yantao Du1, Danping Wang, Lin Luo
1Zhejiang Provincial Key Laboratory of Pathophysiology, Medical School of Ningbo University, Zhejiang, China; Ningbo Institute of Medical Sciences, Medical School of Ningbo University, Ningbo, Zhejiang, China.
Abstract:
MicroRNAs (miRNAs) are the class of small noncoding RNAs, and play an important role in the regulation of gene expression at the posttranscriptional level. In this study, we explored the effect of miR-129-1-3p on the growth and cell cycle of human gastric cancer cell line BGC-823. The miR-129-1-3p mimics or inhibitors were transfected into the BGC-823 cell line, and the cell cycle and cell growth was measured by flow cytometry and real-time cell analyzer, respectively. The possible targets of miR-129-1-3p were analyzed by quantitative real time-PCR (QRT-PCR), Western blotting and Luciferase reporter assay. The results showed that miR-129-1-3p could promote the growth and cell cycle of BGC-823 cells. Although protein expression of programmed cell death 2 (PDCD2) was not changed with miR-129-1-3p, QRT-PCR showed that expression of PDCD2 mRNA was negatively related to the miR-129-1-3p. Luciferase reporter assay revealed that PDCD2 is one of the targets of miR-129-1-3p. Our results indicated that miR-129-1-3p might promote proliferation of BGC-823 cells by targeting PDCD2.
Related Concept Videos
Abnormal Proliferation
TGF - β Signaling Pathway
Mitogens and the Cell Cycle
Cell Specific Gene Expression
Negative Regulator Molecules

