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Updated: Apr 30, 2026

Murine Model for Non-invasive Imaging to Detect and Monitor Ovarian Cancer Recurrence
Published on: November 2, 2014
MiR-718 represses VEGF and inhibits ovarian cancer cell progression
Ruobing Leng1, Lang Zha2, Liangdan Tang1
1Department of Obstetrics and Gynecology, The First Affiliated Hospital of Chongqing Medical University, People's Republic of China.
Abstract:
Oncogenic activation of VEGF is found in various malignancies, including ovarian cancer. In this study, we investigate the role of microRNA (miRNA) in the regulation of VEGF in ovarian cancer. We find that miR-718 is expressed at low levels and inversely correlates with VEGF expression in ovarian cancer specimens. MiR-718 also directly targets and represses VEGF expression. In addition, miR-718 restoration inhibits ovarian cancer proliferation both in vitro and in vivo. Moreover, VEGF expression could reverse the effect of miR-718 on ovarian cancer by increasing the levels of phosphorylated AKT. These results suggest a new therapeutic strategy in ovarian cancer by restoring miR-718 expression, which is involved in VEGF regulation.
Insights
Restoring microRNA-718 (miR-718) expression inhibits ovarian cancer growth by targeting vascular endothelial growth factor (VEGF). This finding offers a potential new therapeutic strategy for ovarian cancer.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Vascular endothelial growth factor (VEGF) oncogenic activation is implicated in various cancers, including ovarian cancer.
- MicroRNAs (miRNAs) are key regulators of gene expression and play critical roles in cancer development.
Purpose of the Study:
- To investigate the role of miR-718 in regulating VEGF expression in ovarian cancer.
- To explore the therapeutic potential of restoring miR-718 in ovarian cancer.
Main Methods:
- Correlation analysis of miR-718 and VEGF expression in ovarian cancer tissues.
- Luciferase reporter assays to confirm direct targeting of VEGF by miR-718.
- In vitro and in vivo assays to assess the effect of miR-718 restoration on ovarian cancer proliferation.
- Western blot analysis to evaluate the impact of VEGF on AKT phosphorylation.
Main Results:
- miR-718 expression is significantly downregulated in ovarian cancer specimens and inversely correlates with VEGF levels.
- miR-718 directly targets and represses VEGF expression.
- Restoration of miR-718 inhibits ovarian cancer cell proliferation in vitro and tumor growth in vivo.
- VEGF overexpression can counteract the anti-proliferative effects of miR-718 by increasing phosphorylated AKT levels.
Conclusions:
- miR-718 acts as a tumor suppressor in ovarian cancer by inhibiting VEGF expression.
- Restoring miR-718 represents a promising therapeutic strategy for ovarian cancer, targeting the VEGF pathway.
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