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Updated: May 9, 2026

Comparing Metastatic Clear Cell Renal Cell Carcinoma Model Established in Mouse Kidney and on Chicken Chorioallantoic Membrane
Published on: February 8, 2020
IMP1 promotes choriocarcinoma cell migration and invasion through the novel effectors RSK2 and PPME1
Yeun-Ting Hsieh1, Min-Min Chou, Hong-Chen Chen
1Department of Life Science, National Chung-Hsing University, 250 Kou-Kuang Rd, Taichung 40227, Taiwan; Department of Obstetrics and Gynecology, Taichung Veterans General Hospital, 1650, Sec. 4, Taiwan Boulevard, Taichung 40705, Taiwan.
Objective:
Oncofetal protein insulin-like growth factor II mRNA-binding protein 1 (IMP1) regulates cellular proliferation and migration. Expression of IMP1 is limited to a few adult human tissues. However, it commonly expresses in a variety of cancers. Our objective was to study the regulatory mechanism of IMP1 on the cellular functions of choriocarcinoma (CC) JAR cells.
Methods:
IMP1 protein levels were measured in CC tissues via immunohistochemistry. Specific siRNAs were used to down-regulate gene expressions. The abilities of migration and invasion were estimated by wound-healing and Matrigel chamber assays. The profile of IMP1-binding genes was investigated with an Agilent microarray. RT-qPCR, RNA immunoprecipitation, and IMP1 rescue experiments were performed to confirm the association between IMP1 and its binding genes. Gene expression was further analyzed by using RT-PCR and Western blotting.
Results:
Strong IMP1 expressions were frequently detected in CC tissues. Knockdown of IMP1 expression in JAR cells inhibited cell migration and invasion, but did not affect cellular proliferation and morphology. Microarray and RNA-immunoprecipitation results revealed several candidate genes regulated by IMP1. Among them, ribosomal protein S6 kinase (RSK2) and protein phosphatase methylesterase 1 (PPME1) were confirmed to be down-regulated in IMP1-depleted JAR cells. Re-expression of IMP1 into the cells restored the expressions of RSK2 and PPME1. Furthermore, the depletion of RSK2 or PPME1 decreased the migration and invasion of JAR cells.
Conclusion:
Our results suggest that IMP1 plays an essential role in the regulation of migration and invasion of human CC cells, possibly through the novel effectors RSK2 and PPME1.
Insights
Insulin-like growth factor II mRNA-binding protein 1 (IMP1) drives choriocarcinoma cell migration and invasion. IMP1 regulates RSK2 and PPME1, key factors in these cellular processes.
Area of Science:
- Oncology
- Molecular Biology
- Cell Biology
Background:
- Oncofetal protein IMP1 is expressed in various cancers, including choriocarcinoma (CC).
- IMP1 regulates cellular proliferation and migration, but its precise role in CC is unclear.
Purpose of the Study:
- To investigate the regulatory mechanism of IMP1 in choriocarcinoma (CC) JAR cells.
- To identify downstream targets of IMP1 involved in CC cell functions.
Main Methods:
- Immunohistochemistry to assess IMP1 levels in CC tissues.
- siRNA-mediated knockdown of IMP1 in JAR cells.
- Wound-healing and Matrigel assays for migration and invasion.
- Microarray, RNA immunoprecipitation, RT-qPCR, RT-PCR, and Western blotting to identify and validate IMP1 targets.
Main Results:
- High IMP1 expression correlated with CC.
- IMP1 knockdown inhibited JAR cell migration and invasion but not proliferation.
- IMP1 regulates the expression of RSK2 and PPME1.
- Downregulation of RSK2 or PPME1 mimicked IMP1 depletion effects on migration and invasion.
Conclusions:
- IMP1 is crucial for choriocarcinoma cell migration and invasion.
- RSK2 and PPME1 are novel downstream effectors of IMP1 in CC.
- Targeting IMP1 may offer a therapeutic strategy for choriocarcinoma.
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