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Published on: August 2, 2024
Circ0004390 promotes cell proliferation through sponging miR-198 in ovarian cancer
Fei Xu1, Mengdong Ni1, Jiajia Li1
1Department of Gynecologic Oncology, Fudan University Shanghai Cancer Center, Shanghai, China; Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China.
Abstract:
Circular RNAs (circRNAs) are a novel class of non-coding RNAs which play important roles in human diseases and tumor progression. However, the function of circRNAs in ovarian cancer remains to be uncovered. Here we found a large amount of circRNAs that are differentially expressed in ovarian cancer tissues compared with normal ovarian tissues. We further identified one circRNA derived from the LPAR3 gene and termed Circ0004390, which was frequently upregulated in ovarian cancer tissues. The knockdown of Circ0004390 can significantly reduce the proliferation of ovarian cancer cells. We further demonstrated that Circ0004390 may promote cell proliferation by acting as a sponge for the miR-198 family to regulated the MET expression in ovarian cancer cells. The level of Circ0004390 was closely related with overall survival of ovarian cancer patients. Our findings suggested that Circ0004390 regulated ovarian cancer proliferation by miR-198/MET axis, which might provide a potential target for the treatment of ovarian cancer.
Insights
Circular RNAs (circRNAs) are implicated in ovarian cancer. Researchers identified Circ0004390, upregulated in tumors, which promotes proliferation by sponging miR-198 to regulate MET, offering a potential therapeutic target.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Circular RNAs (circRNAs) are emerging as critical regulators in human diseases, including cancer.
- The specific roles of circRNAs in ovarian cancer pathogenesis remain largely unexplored.
- This study investigates the function of circRNAs in ovarian cancer progression.
Purpose of the Study:
- To identify differentially expressed circRNAs in ovarian cancer tissues.
- To characterize the function and mechanism of a novel circRNA, Circ0004390, in ovarian cancer.
- To evaluate Circ0004390 as a potential therapeutic target for ovarian cancer.
Main Methods:
- Differential expression analysis of circRNAs in ovarian cancer and normal tissues.
- Functional assays including knockdown of Circ0004390 to assess its impact on cell proliferation.
- Mechanism investigation involving RNA immunoprecipitation and luciferase reporter assays to elucidate the interaction between Circ0004390, miR-198, and MET.
- Correlation analysis between Circ0004390 levels and patient survival data.
Main Results:
- A significant number of circRNAs were found to be differentially expressed in ovarian cancer tissues.
- Circ0004390, derived from the LPAR3 gene, was frequently upregulated in ovarian cancer tissues.
- Knockdown of Circ0004390 significantly inhibited ovarian cancer cell proliferation.
- Circ0004390 acts as a molecular sponge for the miR-198 family, thereby regulating MET expression.
- Higher levels of Circ0004390 correlated with poorer overall survival in ovarian cancer patients.
Conclusions:
- Circ0004390 plays a crucial role in promoting ovarian cancer cell proliferation.
- The Circ0004390/miR-198/MET axis is a key regulatory pathway in ovarian cancer.
- Circ0004390 represents a promising diagnostic biomarker and therapeutic target for ovarian cancer treatment.
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