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Updated: Jun 21, 2026

Conditional Knockdown of Gene Expression in Cancer Cell Lines to Study the Recruitment of Monocytes/Macrophages to the Tumor Microenvironment
Published on: November 23, 2017
APRIL knockdown suppresses migration and invasion of human colon carcinoma cells
Weifeng Ding1, Jinchun Wang, Baolan Sun
1Medical Laboratory Center, Affiliated Hospital of Nantong University, No. 20 Road Xisi, Nantong, Jiangsu, PR China.
Objective:
The purpose of this study was to investigate the function of a proliferation-inducing ligand (APRIL) gene among the metastatic colorectal cancer (CRC) disease.
Methods:
Cell adhesion, cell migration and invasion behavior were detected after knockdown of APRIL expression in the colon carcinoma cell line, SW480 by RNAi and the rescue experiments were performed with recombinant human APRIL (rhAPRIL) in vitro.
Results:
This original study indicated that knockdown of APRIL expression strongly inhibited colon carcinoma cell adhesion, cell migration and invasion in vitro. By contrast, reconstitution of APRIL expression with rhAPRIL in these APRILi cells, prominently restores CRC cell migration and invasion.
Conclusion:
These results strongly suggest that APRIL play an important role in the tumor development of the invasive or migratory behavior of CRC cells and may be a useful therapeutic target in the malignant colon carcinomas.
Insights
Proliferation-inducing ligand (APRIL) promotes colorectal cancer (CRC) cell migration and invasion. Inhibiting APRIL reduces CRC cell adhesion, migration, and invasion, suggesting APRIL as a therapeutic target for colon carcinomas.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Metastatic colorectal cancer (CRC) poses a significant health challenge.
- Understanding the molecular mechanisms driving CRC progression is crucial for developing effective treatments.
Purpose of the Study:
- To investigate the role of proliferation-inducing ligand (APRIL) in the development of metastatic colorectal cancer (CRC).
- To determine if APRIL influences key cellular behaviors associated with cancer metastasis.
Main Methods:
- Knockdown of APRIL expression in the SW480 colon carcinoma cell line using RNA interference (RNAi).
- Assessment of cell adhesion, migration, and invasion following APRIL knockdown.
- Rescue experiments using recombinant human APRIL (rhAPRIL) to restore APRIL expression in knockdown cells.
Main Results:
- APRIL gene knockdown significantly inhibited colon carcinoma cell adhesion, migration, and invasion in vitro.
- Reintroduction of APRIL using rhAPRIL in knockdown cells restored CRC cell migration and invasion capabilities.
- These findings highlight APRIL's direct impact on invasive phenotypes of CRC cells.
Conclusions:
- APRIL plays a critical role in promoting tumor development by enhancing the invasive and migratory behavior of colorectal cancer cells.
- APRIL represents a potential therapeutic target for treating malignant colon carcinomas.
- Targeting APRIL could offer a novel strategy to combat CRC metastasis.
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