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Updated: Feb 2, 2026

Author Spotlight: Unveiling the Role of TMOD3 in Platinum Resistance and Immune Infiltration in Ovarian Cancer
Published on: August 2, 2024
miR-509-3p enhances platinum drug sensitivity in ovarian cancer
Leilei Niu1, Hua Ni2, Yingzi Hou3
1Department of Obstetrics and Gynecology, Third Hospital, Peking University, Beijing 100191, China; Department of Obstetrics and Gynecology, He Nan Provincial People's Hospital, Zhengzhou 450000, China.
Abstract:
Drug-resistance of platinum remains a big challenge for effective treatment of patients with ovarian cancer. MicroRNAs (miRNAs) act as post-transcriptional regulators of gene expression and are associated with multi-drug resistance. Our study aims on identifying role of miRNAs in drug-resistance of platinum in ovarian cancer. In present study, we compared the expression profiles of miRNAs between three pairs of platinum-resistant and platinum-sensitive ovarian tissues and found that miR-509-3p was significantly down-regulated in cisplatin-resistant ovarian cancer tissues. The different expression of miR-509-3p was further determined by RT-qPCR analyses of tissue samples from groups of 20 patients with cisplatin-sensitive ovarian cancer and 7 patients with cisplatin-resistant ovarian cancer. Functional studies demonstrated that miR-509-3p inhibitor decreased cell response to cisplatin (CDDP) and promoted cell survival in SKOV3 ovarian cancer cells. Furthermore, we found gene expression level of Golgi phosphoprotein-3 (GOLPH3) and wntless Wnt ligand secretion mediator (WLS) were regulated by miR-509-3p. The direct bindings of miR-509-3p to GOLPH3 and WLS genes were confirmed by dual-luciferase reporter assay. And the negative correlation between their expression levels in SKOV3 cells was further verified with RT-qPCR. Altogether, our data provide preliminary evidence, supporting that targeting miR-509-3p might be a potential therapeutic strategy for patients with platinum-resistant ovarian cancer.
Insights
MicroRNAs regulate gene expression and drug resistance. This study found miR-509-3p is down-regulated in platinum-resistant ovarian cancer, suggesting it
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Platinum-based chemotherapy is a cornerstone in ovarian cancer treatment.
- Drug resistance, particularly to platinum agents, significantly limits treatment efficacy.
- MicroRNAs (miRNAs) are key regulators of gene expression implicated in multi-drug resistance.
Purpose of the Study:
- To investigate the role of specific microRNAs in platinum drug resistance in ovarian cancer.
- To identify potential miRNA biomarkers for platinum-resistant ovarian cancer.
Main Methods:
- Comparative miRNA expression profiling of platinum-resistant versus sensitive ovarian cancer tissues.
- Quantitative reverse transcription polymerase chain reaction (RT-qPCR) for miR-509-3p validation.
- In vitro functional assays using SKOV3 ovarian cancer cells to assess the impact of miR-509-3p inhibition on cisplatin sensitivity.
- Dual-luciferase reporter assays to confirm direct targeting of GOLPH3 and WLS by miR-509-3p.
Main Results:
- miR-509-3p was significantly downregulated in cisplatin-resistant ovarian cancer tissues and cells.
- Inhibition of miR-509-3p reduced cellular response to cisplatin and promoted cell survival.
- miR-509-3p directly targets and negatively regulates the expression of Golgi phosphoprotein-3 (GOLPH3) and wntless Wnt ligand secretion mediator (WLS).
Conclusions:
- Downregulation of miR-509-3p is associated with platinum resistance in ovarian cancer.
- miR-509-3p may play a crucial role in modulating chemoresistance by targeting GOLPH3 and WLS.
- Targeting miR-509-3p presents a potential therapeutic strategy for overcoming platinum resistance in ovarian cancer.
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