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Updated: Jul 14, 2026

Heterotypic Three-dimensional In Vitro Modeling of Stromal-Epithelial Interactions During Ovarian Cancer Initiation and Progression
Published on: August 28, 2012
[Expression of phosphatidylinositol-3 kinase in epithelial ovarian carcinoma]
1Department of Gynecology, Obstetrics and Gynecology Hospital, Fudan University, Shanghai 200011, China.
Objective:
To explore the expression and significance of phosphatidylinositol-3 kinase (PI3K) in ovarian cancer, and the effect of combined PI3K inhibitor (LY294002) therapy with cisplatin on epithelial ovarian carcinoma, and to explore if there is a synergistic effect between the two therapies.
Methods:
The expression levels of PI3K p85 subunit proteins and mRNA were evaluated by western blot and RT-PCR in normal ovarian tissue (G1), ovarian benign tumor tissue (G2), ovarian borderline tumor tissue (G3) and ovarian cancer tissue (G4), and the relevant clinical pathological parameters were analyzed. SKOV3 cells were isolated and cultured by enzymolysis method. SKOV3 cells were treated with culture medium only, LY294002 (1, 10, 30, 50, 100 micromol/L), cisplatin (0.33, 1.25, 2.5, 5, 10 micromol/L), LY294002 (50 micromol/L) + cisplatin (10 micromol/L) for 2 days, respectively. The effect of LY294002 and cisplatin on the growth of SKOV3 cells was measured by methyl thiazolyl tetrazolium assay.
Results:
There was no positive expression of PI3K p85 subunit proteins in G1 and G2, while the expression was 2/6 in G3, and 85% (33/39) in G4. PI3K p85 subunit mRNA expression levels were 0.178 +/- 0.102 in G1, 0.643 +/- 0.112 in G2, 0.847 +/- 0.058 in G3, 1.689 +/- 0.423 in G4; there was a significant difference between G1, G2, G3 and G4 (P<0.01). There was no significant correlation between protein expression and age at surgery or clinico-pathological staging (P>0.05). Significant differences were noted between protein expression levels in G4 (III, IV) and G4 (I, II; P<0.05). There was a significant difference between expression levels in tissues of different differentiation degrees (P<0.05). LY294002 and cisplatin inhibited the growth of SKOV3 cell in a concentration-dependent manner. The inhibitory activity of LY294002 at the concentration of 50 micromol/L was (46.0 +/- 2.0)% after treatment for two days. The inhibitory activity of cisplatin at the concentration of 10 micromol/L was (44.4 +/- 3.2)% after treatment for two days. After treatment for two days, the inhibitory activity of LY294002 50 micromol/L + cisplatin 10 micromol/L was (57.1 +/- 4.1)%. The inhibition effect on SKOV3 cell growth of the combined treatment group was better than the LY294002 or cisplatin treated group (P<0.01).
Conclusions:
PI3K p85 subunit is highly expressed and positively correlated with ovarian cancer. Different expression levels exist in tissues of late ovarian cancer, earlier ovarian cancer, borderline tumor, benign ovarian tumor and normal ovarian tissue. The changes in PI3K p85 subunit are correlated with tumor differentiation degree, but not pathologic typing. LY294002 combined with cisplatin can significantly enhance the killing efficiency in ovarian cancer cells.
Insights
Phosphatidylinositol-3 kinase (PI3K) p85 subunit is highly expressed in ovarian cancer, correlating with tumor progression. Combining PI3K inhibitor LY294002 with cisplatin synergistically enhances cancer cell killing efficiency.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Ovarian cancer is a leading cause of cancer-related deaths in women.
- Phosphatidylinositol-3 kinase (PI3K) signaling pathway plays a critical role in cell growth, proliferation, and survival.
- Dysregulation of PI3K is implicated in various cancers, including ovarian cancer.
Purpose of the Study:
- To investigate the expression and clinical significance of PI3K p85 subunit in ovarian cancer.
- To evaluate the efficacy of combined therapy using PI3K inhibitor LY294002 and cisplatin in epithelial ovarian carcinoma.
- To determine if a synergistic effect exists between LY294002 and cisplatin treatment.
Main Methods:
- Western blot and RT-PCR were used to assess PI3K p85 subunit protein and mRNA expression in normal ovarian tissue, benign tumors, borderline tumors, and ovarian cancer tissues.
- SKOV3 ovarian cancer cells were treated with LY294002, cisplatin, or a combination of both.
- Cell viability was measured using the methyl thiazolyl tetrazolium (MTT) assay.
Main Results:
- PI3K p85 subunit expression was significantly higher in ovarian cancer tissues compared to normal and benign tissues, and correlated with tumor differentiation.
- Both LY294002 and cisplatin inhibited SKOV3 cell growth in a dose-dependent manner.
- The combination of LY294002 (50 µmol/L) and cisplatin (10 µmol/L) demonstrated a significantly enhanced inhibitory effect on SKOV3 cell growth compared to either agent alone.
Conclusions:
- PI3K p85 subunit is overexpressed in ovarian cancer and its levels correlate with tumor progression and differentiation.
- Combined treatment with LY294002 and cisplatin exhibits a synergistic effect, significantly improving the killing efficiency of ovarian cancer cells.
- This study supports the potential of targeting the PI3K pathway in combination with chemotherapy for ovarian cancer treatment.
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