Related Experiment Video
Updated: Jun 23, 2026

Assessing Cell Viability and Death in 3D Spheroid Cultures of Cancer Cells
Published on: June 16, 2019
Effect of proliferation, cell cycle, and Bcl-2s of MCF-7 cells by resveratrol
Yi-Zheng Wang1, Bo Cao, Shao-Xiong Li
1Tianjin Key Laboratory for Biomarkers of Occupational and Environmental Hazard, Tianjin, China.
Abstract:
Our goals were to examine the dual-directional regulation effects of resveratrol (1) in vitro by using MCF-7 cells (estradiol receptor-positive cells), study its mechanism of action, and give a systematical analysis of the regulatory networks of each related factor. An MTT test and growth curve showed that the proliferation of MCF-7 cells was inhibited by a high concentration of 1, and that its IC(50) was 8.70 x 10(-5) +/- 0.23 mol/l. However, 1 induced the proliferation of MCF-7 cells at 10(-7)-10(-5) mol/l, and resulted in a peak proliferation at 1.0 x 10(-7) mol/l. A high concentration of 1 arrested cell cycle progression at the G(1) phase, and a typical "sub-G(1) peak" of apoptotic cells was also observed by flow cytometry. The proliferation index of MCF-7 cells increased significantly with a low concentration of 1 (p < 0.05). 1 in high concentrations induced Bax, caspase-3, and cyclin-dependent kinase (CDK) inhibitor P21 expression, whereas the expressions of cyclin CDK2, Bcl-2, and proliferating cell nuclear antigen (PCNA) were decreased by 1 treatment. Conversely, treatment with low concentrations of 1 decreased the expression of P21 and Bax, while the expressions of cyclin CDK2, Bcl-2, and PCNA were increased. These results suggest that 1 had a dual-regulatory effect on MCF-7 cells. CDK-associated protein was a key factor at both the high and low concentrations used in this study.
Insights
Resveratrol exhibits dual effects on MCF-7 cells: high concentrations inhibit proliferation and induce apoptosis, while low concentrations stimulate cell growth. Cyclin-dependent kinase (CDK) associated proteins play a key role in these regulatory networks.
Area of Science:
- Molecular Biology
- Cell Biology
- Pharmacology
Background:
- Resveratrol, a natural polyphenol, is known for its potential health benefits.
- MCF-7 cells are a widely used human breast cancer cell line, positive for estradiol receptors.
- Understanding the dose-dependent effects of compounds like resveratrol is crucial for therapeutic applications.
Purpose of the Study:
- To investigate the dual-directional regulatory effects of resveratrol on MCF-7 cells in vitro.
- To elucidate the mechanism of action of resveratrol in these cells.
- To systematically analyze the regulatory networks influenced by resveratrol.
Main Methods:
- MTT assay and growth curve analysis to assess cell proliferation.
- Flow cytometry to analyze cell cycle progression and apoptosis.
- Western blotting or similar techniques to evaluate the expression of key proteins (Bax, caspase-3, P21, cyclin CDK2, Bcl-2, PCNA).
Main Results:
- Resveratrol demonstrated a dual effect: high concentrations (IC50 = 8.70 x 10(-5) mol/l) inhibited MCF-7 cell proliferation and induced G1 phase arrest and apoptosis.
- Low concentrations (10(-7)-10(-5) mol/l) stimulated MCF-7 cell proliferation, with peak effect at 1.0 x 10(-7) mol/l.
- High concentrations increased Bax, caspase-3, and P21 expression while decreasing cyclin CDK2, Bcl-2, and PCNA. Low concentrations showed opposite effects on these proteins.
Conclusions:
- Resveratrol exerts a dose-dependent, dual regulatory effect on MCF-7 cells.
- CDK-associated proteins are identified as key factors in resveratrol's regulatory network at both high and low concentrations.
- These findings provide insights into the complex mechanisms of resveratrol in breast cancer cells.
More Related Videos
Related Concept Videos
Molecular Factors Affecting Cell Division
Several proteins function as internal regulators to ensure each cell cycle stage is completed faithfully before proceeding to the next. Regulator molecules may act directly or influence the activity or production of other...
Abnormal Proliferation
Cells Coordinate Growth and Proliferation
Negative Regulator Molecules
Replicative Cell Senescence
The Cell Cycle Control System

