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Updated: Apr 15, 2026

Author Spotlight: Unveiling the Role of TMOD3 in Platinum Resistance and Immune Infiltration in Ovarian Cancer
Published on: August 2, 2024
MicroRNA signatures of platinum-resistance in ovarian cancer
Objectives:
The authors utilized a microRNA (miRNA) array to compare the differentially expressed miRNAs in platinum-resistant associated ovarian cancer cells.
Materials And Methods:
The differential expression of microRNA between COC1 (DDP-sensitive) and platinum-resistant COC1/DDP (DDP-resistant) tumor cell lines was determined using microarray. Expression levels were further validated by real-time quantitive polymerase chain reaction (qRT-PCR).
Results:
The authors identified that several miRNAs are altered in collected 86 samples of human ovarian cancer cell-lines, with four significantly deregulated miRNAs and 13 upregulated miRNAs. Of which, miR-141-3p was the most differentially expressed miRNA between COC1 group (1.7833 ± 0.7213) and COC1/DDP group (14.0433 ± 4.4895) (p < 0.05). Additionally, the product curve of PCR amplification indicated that miR-141-3p had a significant higher expression level in chemotherapy resistant group (n = 20) rather than in chemotherapy sensitive group (n = 20) (9.56 ± 1.04 vs. 1.59 ± 0.91, p < 0.05).
Conclusions:
The present results suggest that miR-141-3p might be used as a therapeutic target to modulate platinum-based chemotherapy and as a biomarker to predict chemotherapy response.
Insights
This study identified miR-141-3p as a significantly upregulated microRNA in platinum-resistant ovarian cancer cells. It shows potential as a therapeutic target and biomarker for predicting chemotherapy response.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Ovarian cancer often develops platinum resistance, necessitating novel therapeutic strategies.
- MicroRNAs (miRNAs) play crucial roles in cancer development and drug resistance.
- Identifying specific miRNAs associated with platinum resistance is vital for improving treatment outcomes.
Purpose of the Study:
- To compare differentially expressed miRNAs in platinum-resistant ovarian cancer cells.
- To identify potential biomarkers for predicting response to platinum-based chemotherapy.
Main Methods:
- Utilized miRNA array technology to analyze miRNA expression profiles.
- Compared miRNA expression between platinum-sensitive (COC1) and platinum-resistant (COC1/DDP) ovarian cancer cell lines.
- Validated differential expression using real-time quantitative polymerase chain reaction (qRT-PCR).
Main Results:
- Identified several differentially expressed miRNAs in ovarian cancer cell lines.
- Found four significantly deregulated and 13 upregulated miRNAs.
- miR-141-3p exhibited the most significant differential expression, being highly upregulated in platinum-resistant cells (p < 0.05).
- qRT-PCR confirmed significantly higher miR-141-3p expression in chemotherapy-resistant versus sensitive groups (p < 0.05).
Conclusions:
- miR-141-3p is a promising candidate for therapeutic targeting to overcome platinum resistance.
- miR-141-3p may serve as a valuable biomarker for predicting patient response to platinum-based chemotherapy.
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