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Updated: Jun 29, 2025

Author Spotlight: Unveiling the Role of TMOD3 in Platinum Resistance and Immune Infiltration in Ovarian Cancer
Published on: August 2, 2024
Anlotinib Inhibits Ovarian Cancer and Enhances Cisplatinum Sensitivity via Suppressing NOTCH2 Expression and Stemness
Xiaosheng Xu1, Qun Wang1, Lifei Shen1
1Department of Obstetrics and Gynecology, Ruijin Hospital, Shanghai Jiao Tong University, School of Medicine, Shanghai, P.R. China.
Background/Aim:
The prognosis of ovarian cancer (OC) patients is especially poor for patients with chemotherapy resistance. Anlotinib, a novel multi-targeted tyrosine kinase inhibitor, has shown encouraging clinical efficacy in several tumor types. The aim of the present study was to examine the inhibitory efficacy and mechanism of anlotinib on the proliferation and chemosensitivity of OC cells.
Materials And Methods:
The inhibitory effects of Anlotinib on SKOV3 and OVCAR3 OC cells were examined using CCK-8 cell-viability, colony-formation, flow-cytometry, transwell-migration and sphere-formation assays. A xenograft mouse model was used for in vivo studies. RT-qPCR and western blotting were used to detect gene expression.
Results:
Molecular targets of anlotinib were elevated in OC patient tumors. Anlotinib significantly inhibited ovarian cancer cell proliferation and migration in vitro. Anlotinib enhanced the sensitivity of ovarian cancer cells to cisplatinum both in vitro and in vivo. Anlotinib suppressed sphere formation and the stemness phenotype of OC cells by inhibiting NOTCH2 expression.
Conclusion:
Anlotinib inhibits ovarian cancer and enhances cisplatinum sensitivity, suggesting its future clinical promise.
Insights
Anlotinib effectively inhibits ovarian cancer (OC) cell proliferation and migration. This multi-targeted tyrosine kinase inhibitor also enhances chemotherapy sensitivity, showing promise for OC treatment.
Area of Science:
- Oncology
- Pharmacology
Background:
- Ovarian cancer (OC) poses a poor prognosis, particularly with chemotherapy resistance.
- Anlotinib, a multi-targeted tyrosine kinase inhibitor, demonstrates efficacy across various cancers.
Purpose of the Study:
- To investigate the inhibitory effects of anlotinib on ovarian cancer cell proliferation.
- To determine anlotinib's mechanism in modulating ovarian cancer cell chemosensitivity.
Main Methods:
- In vitro assays (CCK-8, colony-formation, flow-cytometry, transwell-migration, sphere-formation) were used on OC cell lines.
- In vivo xenograft mouse models and molecular analyses (RT-qPCR, western blotting) were employed.
Main Results:
- Anlotinib significantly inhibited proliferation and migration of ovarian cancer cells in vitro.
- The drug enhanced ovarian cancer cell sensitivity to cisplatin both in vitro and in vivo.
- Anlotinib suppressed sphere formation and stemness by inhibiting NOTCH2 expression.
Conclusions:
- Anlotinib demonstrates inhibitory effects on ovarian cancer.
- The drug enhances cisplatin sensitivity in ovarian cancer, indicating potential clinical utility.
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