Volume 12, Issue 3 (Aug & Sep 2018)
payavard 2018, 12(3): 221-229 |
Back to browse issues page
Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:
Valizadeh M, Rouhi L, Hejazi S H. The Viability and Pro Apoptotic Effect of Green Tea on Breast Cancer Cell Line (SK-BR-3) and Human Fibroblast Cells (HU-02). payavard 2018; 12 (3) :221-229
URL: http://payavard.tums.ac.ir/article-1-6573-en.html
URL: http://payavard.tums.ac.ir/article-1-6573-en.html
1- Biology Department, School of Basic Sciences, Islamic Azad University, Shahrekord Branch, Shahrekord, Iran
2- Biology Department, School of Basic Sciences, Islamic Azad University, Shahrekord Branch, Shahrekord, Iran ,Lrouhi59@gmail.com
3- Biology Department, School of Basic Sciences, Islamic Azad University, Shahrekord Branch, Shahrekord, Iran - Parasitology & Mycology Department, School of Medicine, Skin Diseases and Leishmaniosis Research Center, Isfahan University of Medical Sciences, Isfahan, Iran
2- Biology Department, School of Basic Sciences, Islamic Azad University, Shahrekord Branch, Shahrekord, Iran ,
3- Biology Department, School of Basic Sciences, Islamic Azad University, Shahrekord Branch, Shahrekord, Iran - Parasitology & Mycology Department, School of Medicine, Skin Diseases and Leishmaniosis Research Center, Isfahan University of Medical Sciences, Isfahan, Iran
Abstract: (3391 Views)
Background and Aim: Breast cancer is one of the most common types of cancers and is the second leading cause of death form of cancer in women. In recent years, many scientific and medical studies have shown that Green tea has anti-proliferative, anti-mutagenic, anti-oxidant, antibacterial and antiviral effects. Some Green tea polyphenols have anti-cancer activity. In the present study, the effect of Green tea extract was evaluated on the Breast cancer cell line (SK-BR-3) and compared with human fibroblast cell line (HU-02).
Materials and Methods: SK-BR-3 and HU-02 cell lines were treated for 24, 48 and 72 hours with different concentrations of Green tea (50, 100, 200, 400 and 800 μg/ml). Then, Bioavailability was analyzed by MTT kit and Apoptosis was analyzed by flow cytometry using an Annexin V-FITS Kit.
Results: With increasing concentrations of Green tea extract in dose and time dependent manner, bioavailability of cells showed a decrease as compared to control group. Increased incidence of apoptosis was significantly higher in other experimental groups than the control group, while the concentration of 800 μg/ml of Green tea extract was more effective in SKBR3 cell line. Green tea did not show significant effect in HU-02 cells.
Conclusion: Due to the fact that cell proliferation and abnormal apoptosis are one of the main characteristics of cancer cells, Green tea can be used to reduce cell proliferation and increase apoptosis in prevention and treatment of Breast cancer.
Materials and Methods: SK-BR-3 and HU-02 cell lines were treated for 24, 48 and 72 hours with different concentrations of Green tea (50, 100, 200, 400 and 800 μg/ml). Then, Bioavailability was analyzed by MTT kit and Apoptosis was analyzed by flow cytometry using an Annexin V-FITS Kit.
Results: With increasing concentrations of Green tea extract in dose and time dependent manner, bioavailability of cells showed a decrease as compared to control group. Increased incidence of apoptosis was significantly higher in other experimental groups than the control group, while the concentration of 800 μg/ml of Green tea extract was more effective in SKBR3 cell line. Green tea did not show significant effect in HU-02 cells.
Conclusion: Due to the fact that cell proliferation and abnormal apoptosis are one of the main characteristics of cancer cells, Green tea can be used to reduce cell proliferation and increase apoptosis in prevention and treatment of Breast cancer.
Send email to the article author
| Rights and permissions | |
 |
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. |
