Title of article :
Apoptosis Induction with Combined Use of Cisplatin and Fisetin in Cisplatin- Resistant Ovarian Cancer Cells (A2780)
Author/Authors :
Jafarzadeh, S Department of Biology - Mashhad branch - Islamic Azad University - Mashhad, Iran , Baharara, J Department of Biology - Mashhad branch - Islamic Azad University - Mashhad, Iran , Tehranipour, M Department of Biology - Mashhad branch - Islamic Azad University - Mashhad, Iran
Abstract :
Ovarian cancer is the leading cause of death caused by genital cancers.
One of the most common treatments for this type of cancer is chemotherapy by cisplatin,
which induces apoptosis in cancer cells. Apoptosis is a type of physiological cell
death. Cisplatin chemotherapy usually has several side effects and cellular resistance
to cisplatin is a common incidence. In order to overcome these problems, the use of
combination therapies using natural substances has been considered. Fisetin is a flavonoid
with anti-cancer activity which induces apoptosis .In this study, the apoptosis
induced by cisplatin along with Fisetin in cisplatin-resistant ovarian cancer cell line
(A2780) was investigated.
Methods: In the present experimental study, the effect of combined use of Fisetin and
cisplatin on ovarian cancer cell lines (A2780) was investigated by using MTT assay.
Cell death was also determined by DAPI, acridine orange/propidium iodide, and Annexin/
PI assay. Apoptotic gene expression of Bax, BCL-2, caspase 3, and caspase 9 was
also assessed by real time PCR.
Results: The results of MTT assay indicated that the combined treatment of Fisetin
and cisplatin effectively inhibits proliferation of A2780 cells. The results of DAPI staining
showed that fragmentation of chromatin in cells occurred in the combined treatment.
Acridine orange-propidium iodide staining and Annexin/PI staining showed an
increase in the rate of apoptotic cells in cells under combined treatment. The results of
the study regarding changes in gene expression also indicated that Bax pro-apoptotic
gene expression and BCL-2 anti-apoptotic gene expression increased in cells under
treatment; moreover, gene expression of caspases 3 and 9 significantly increased as
well.
Conclusion: According to the findings of this study, the combined use of cisplatin and
Fisetin increases the induction of apoptosis in cisplatin-resistant ovarian cancer cells
(A2780); therefore, the combined use of cisplatin and Fisetin can be considered a
promising strategy in the treatment of ovarian cancer.
Keywords :
Ovarian neoplasms , Fisetin , Cisplatin , Apoptosis
Journal title :
AJMB Avicenna Journal of Medical Biotechnology