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Published on: August 2, 2024
LncRNA-MSC-AS1 inhibits the ovarian cancer progression by targeting miR-425-5p
Yinling Zhao1, Donglan Yuan2, Dandan Zhu1
1Department of Obstetrics and Gynaecology, Taizhou People's Hospital, 399 Hailing South Road, Taizhou, 225300, Jiangsu, China.
Background:
Long non-coding RNAs (lncRNAs) and microRNAs (miRNAs) were reported to be aberrantly expressed and related to the pathogenesis of ovarian cancer. However, the role and regulatory mechanism of MSC-AS1 in ovarian cancer has yet to be fully elucidated.
Methods:
Expression of lncRNA MSC-AS1 (MSC-AS1) and microRNA-425-5p (miR-425-5p) in the ovarian cancer tissue samples and cell lines was examined by quantitative real-time polymerase chain reaction (qRT-PCR). The functions of MSC-AS1 on ovarian cancer cell proliferation, cell cycle and apoptosis were determined using MTT, colony formation and flow cytometry analyses. The protein expression levels were evaluated using western blot assay. The targeting relationship MSC-AS1 and miR-425-5p was verified via dual-luciferase reporter assay.
Results:
MSC-AS1 expression level was lowly expressed, while miR-425-5p level was highly in ovarian cancer tissues and cells. Elevation of MSC-AS1 has the ability to significantly inhibit cell proliferation and facilitate cell apoptosis in SKOV3 and A2780 cells. Moreover, MSC-AS1 targeted and negatively modulated miR-425-5p. MiR-425-5p up-regulation has been proved to partially reverse the tumor suppressive function of MSC-AS1 overexpression CONCLUSION: MSC-AS1 sponged miR-425-5p to inhibit the ovarian cancer progression. These findings may provide a promising therapeutic target for the treatment of ovarian cancer.
Insights
Long non-coding RNA MSC-AS1 inhibits ovarian cancer progression by sponging microRNA-425-5p. This interaction suppresses cell proliferation and promotes apoptosis, offering a potential therapeutic target for ovarian cancer treatment.
Area of Science:
- Molecular Biology
- Oncology
- Genetics
Background:
- Aberrant expression of long non-coding RNAs (lncRNAs) and microRNAs (miRNAs) is linked to ovarian cancer pathogenesis.
- The specific role and regulatory mechanisms of lncRNA MSC-AS1 in ovarian cancer remain unclear.
Purpose of the Study:
- To investigate the role of lncRNA MSC-AS1 in ovarian cancer.
- To elucidate the regulatory mechanism of MSC-AS1 involving microRNA-425-5p in ovarian cancer.
Main Methods:
- Quantitative real-time PCR (qRT-PCR) to assess MSC-AS1 and miR-425-5p expression in ovarian cancer tissues and cell lines.
- MTT, colony formation, and flow cytometry assays to evaluate MSC-AS1 function on cell proliferation, cell cycle, and apoptosis.
- Western blot for protein expression analysis and dual-luciferase reporter assay to confirm the targeting relationship between MSC-AS1 and miR-425-5p.
Main Results:
- MSC-AS1 was lowly expressed, while miR-425-5p was highly expressed in ovarian cancer tissues and cells.
- Overexpression of MSC-AS1 inhibited ovarian cancer cell proliferation and induced apoptosis in SKOV3 and A2780 cells.
- MSC-AS1 directly targeted and negatively regulated miR-425-5p; miR-425-5p upregulation partially reversed the tumor-suppressive effects of MSC-AS1.
Conclusions:
- MSC-AS1 acts as a tumor suppressor in ovarian cancer by sponging miR-425-5p, thereby inhibiting cancer progression.
- The MSC-AS1/miR-425-5p axis represents a potential therapeutic target for ovarian cancer treatment.
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