Related Experiment Video
Updated: Jul 5, 2025

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
miR-129-2-3p inhibits colon cancer cell proliferation by down-regulating the expression of BZW1
Liang Tao1, Peng Song1, Lihua Shao1
1Department of Gastrointestinal Surgery, Nanjing Drum Tower Hospital, the Affiliated Hospital of Nanjing University Medical School, Nanjing 210008, Jiangsu Province, China.
Background And Study Aims:
MicroRNA (miRNA) is involved in diverse biological and physiological processes of tumors. Dysregulation of miRNA will induce a series of human diseases. miR-129-2-3p has vital effects in the pathogenesis of various tumors. However, the regulatory function of miR-129-2-3p in colon cancer remains to be clarified. This study investigated the role of miR-129-2-3p targeting BZW1 in proliferation, apoptosis, migration, and invasion of colon cancer.
Patients And Methods:
Here, RT-qPCR was applied to measure the miR-129-2-3p levels in colon cancer tissues. The predicted targets of miR-129-2-3p were identified by bioinformatics and verified using luciferase reporter assay. The effects of miR-129-2-3p on colon cancer were detected by CCK-8, colony formation, transwell chamber test, wound healing, and flow cytometry assays. Finally, the influence of miR-129-2-3p on tumor growth was studied. Nude mice were xenografted with transfected Lovo cells by subcutaneous injection of 5 × 105 cells in 100 µl. HE staining and TUNEL were used to assess metastasis ability.
Results:
miR-129-2-3p level in colon cancer tissue was significantly reduced. Furthermore, it was verified that BZW1 was a target of miR-129-2-3p, and its expression in colon cancer cells was inhibited by miR-129-2-3p. Additionally, miR-129-2-3p inhibited colon cancer cell proliferation, colony formation, mobility ability and tumor growth, and promoted cell apoptosis by targeting BZW1. miR-129-2-3p overexpression in tumor xenografts in vivo decreased BZW1 expression, and suppressed tumor growth.
Conclusion:
Collectively, these findings indicated that miR-129-2-3p exerts a suppressive role in colon cancer cells by directly targeting BZW1, and may have significant therapeutic implications for patients with colon cancer.
Insights
MicroRNA 129-2-3p (miR-129-2-3p) is downregulated in colon cancer and inhibits tumor growth by targeting BZW1. Restoring miR-129-2-3p may offer a therapeutic strategy for colon cancer patients.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- MicroRNAs (miRNAs) play crucial roles in tumor development and progression.
- Dysregulation of specific miRNAs, like miR-129-2-3p, is implicated in various cancers.
- The precise role of miR-129-2-3p in colon cancer pathogenesis requires further elucidation.
Purpose of the Study:
- To investigate the regulatory function of miR-129-2-3p in colon cancer.
- To determine if miR-129-2-3p targets BZW1 in colon cancer cells.
- To assess the impact of miR-129-2-3p on colon cancer cell proliferation, apoptosis, migration, and invasion.
Main Methods:
- Quantitative reverse transcription polymerase chain reaction (RT-qPCR) to measure miR-129-2-3p levels.
- Bioinformatics and luciferase reporter assays to identify and validate BZW1 as a miR-129-2-3p target.
- In vitro assays (CCK-8, colony formation, Transwell, wound healing, flow cytometry) to evaluate cellular effects.
- In vivo xenograft studies in nude mice to assess tumor growth and metastasis.
Main Results:
- miR-129-2-3p expression was significantly reduced in colon cancer tissues.
- BZW1 was confirmed as a direct target of miR-129-2-3p, with its expression inhibited by miR-129-2-3p.
- Overexpression of miR-129-2-3p suppressed colon cancer cell proliferation, colony formation, migration, invasion, and tumor growth, while promoting apoptosis.
- In vivo, miR-129-2-3p overexpression reduced BZW1 levels and inhibited tumor growth.
Conclusions:
- miR-129-2-3p acts as a tumor suppressor in colon cancer by directly targeting BZW1.
- This miRNA holds potential as a therapeutic agent for colon cancer treatment.
Related Concept Videos
MicroRNAs
Abnormal Proliferation
Role Of Notch Signalling In Intestinal Stem Cell Renewal
Direct cell-to-cell contact is needed for the activation of Notch signaling. The signal is initiated when a notch ligand binds to a receptor on an adjacent cell, also...
Negative Regulator Molecules

