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In vitro Enrichment of Ovarian Cancer Tumor-initiating Cells
Published on: February 18, 2015
Effects of ginsenoside Rg3 on epigenetic modification in ovarian cancer cells
Lingqin Zhao1, Huafeng Shou1, Lu Chen1
1Department of Gynecological Oncology, Zhejiang Cancer Hospital, Hangzhou, Zhejiang 310022, P.R. China.
Abstract:
Epigenetic modifications are closely related to oncogene activation and tumor suppressor gene inactivation. The aim of this study was to determine the effects of ginsenoside Rg3 on epigenetic modification in ovarian cancer cells. Cell proliferation, metastasis, invasion and apoptosis were respectively determined using Cell Counting Kit‑8 (CCK‑8), wound healing, Transwell and flow cytometric assays. Methylation levels were determined using methylation specific PCR (MSP). Related‑factor expression was detected by conducting real‑time‑qPCR (RT‑qPCR) and western blotting. The results revealed that cell proliferation was inhibited by ginsenoside Rg3 (0, 25, 50, 100 and 200 µg/ml) in a time‑dependent manner (12, 24 and 48 h). Ginsenoside Rg3 (50, 100 and 200 µg/ml) was selected to treat cells in various experiments. When ovarian cells were treated with ginsenoside Rg3, cell apoptosis was observed to be promoted, while cell metastasis and invasion were inhibited at 48 h. The results of the present study revealed that in the promoter regions of p53, p16 and hMLH1, the methylation levels decreased, while the mRNA and protein levels significantly increased. The activities of DNMTs and mRNA as well as protein levels of DNMT1, DNMT3a and DNMT3b were decreased by Rg3. The data also demonstrated that the mRNA and protein levels of acetyl‑H3 K14/K9 and acetyl‑H4 K12/K5/K16 were increased by Rg3. Hence, ginsenoside Rg3 inhibited ovarian cancer cell viability, migration and invasion as well as promoted cell apoptosis.
Insights
Ginsenoside Rg3 inhibits ovarian cancer cell growth and spread by altering epigenetic modifications. This compound promotes apoptosis and reduces tumor cell proliferation, migration, and invasion.
Area of Science:
- Oncology
- Epigenetics
- Pharmacology
Background:
- Epigenetic modifications are crucial in cancer development, influencing oncogene activation and tumor suppressor gene inactivation.
- Ovarian cancer is a significant health concern, necessitating novel therapeutic strategies.
- Ginsenosides, particularly Rg3, have shown potential anti-cancer properties.
Purpose of the Study:
- To investigate the effects of ginsenoside Rg3 on epigenetic modifications in ovarian cancer cells.
- To evaluate the impact of ginsenoside Rg3 on ovarian cancer cell behavior, including proliferation, apoptosis, metastasis, and invasion.
Main Methods:
- Cell Counting Kit-8 (CCK-8), wound healing, Transwell, and flow cytometry assays were used to assess cell viability, migration, invasion, and apoptosis.
- Methylation-specific PCR (MSP) was employed to determine DNA methylation levels.
- Real-time quantitative PCR (RT-qPCR) and western blotting were utilized to detect gene and protein expression.
Main Results:
- Ginsenoside Rg3 inhibited ovarian cancer cell proliferation in a time-dependent manner.
- Treatment with ginsenoside Rg3 promoted apoptosis and inhibited metastasis and invasion of ovarian cancer cells.
- Rg3 decreased methylation levels in the promoter regions of p53, p16, and hMLH1, leading to increased mRNA and protein expression.
- Ginsenoside Rg3 reduced the activity and expression of DNA methyltransferases (DNMTs) while increasing histone acetylation.
Conclusions:
- Ginsenoside Rg3 demonstrates significant anti-cancer effects against ovarian cancer cells by modulating epigenetic mechanisms.
- The findings suggest that ginsenoside Rg3 is a promising agent for ovarian cancer therapy, capable of inhibiting cell viability, migration, and invasion while promoting apoptosis.
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