Author/Authors :
Amini Chermahini, Fatemeh Cellular and Molecular Research Center - Shahrekord University of Medical Sciences, Shahrekord, Iran , Raeisi, Elham Department of Medical Physics and Radiology - School of Allied Medical Sciences - Shahrekord University of Medical Sciences, Shahrekord, Iran , Aazami, Mathias Hossain Department of Cardiology and Cardiac Surgery - School of Medicine - Shahrekord University of Medical Sciences, Shahrekord, Iran , Mirzaei, Abbas Cellular and Molecular Research Center - Shahrekord University of Medical Sciences, Shahrekord, Iran , Heidarian, Esfandiar Clinical Biochemistry Research Center - Shahrekord University of Medical Sciences, Shahrekord, Iran , Lemoigne, Yves Department of Medical Physics - Institute for Medical Physics, Ambilly, France
Abstract :
Background: Bromelain enhances anticancer impacts to chemotherapeutic agents. The question as to whether bromelain does promote in-vitro cytotoxic and proapoptotic effects of cisplatin on human prostatic carcinoma PC3 cell line was investigated. Materials and Methods: PC3 (human prostatic carcinoma) cells were treated either single or in combination with bromelain and/or cisplatin. MTT, clonogenic assay, flow cytometry and real-time quantitative polymerase chain reaction were used to investigate cell viability, colony formation, proapoptotic potential and p53 gene expression, respectively. Results: Cisplatin (IC10) combined with bromelain (IC40) significantly affected PC3 cell viability, inhibited colony formation, as well increased p53 proapoptotic gene expression compared to cisplatin single treatment. Nevertheless, bromelain-cisplatin chemoherbal combination did not display any additive proapoptotic effect compared to single treatments. Conclusion: Bromelain-cisplatin chemoherbal combination demonstrated synergistic in-vitro anticancer effect on human prostatic carcinoma cell line, PC3, that drastically reduced required cisplatin dose.
Keywords :
PC3 Cells , Bromelain , Cisplatin , Synergistic Effect , Clonogenic Cell Assay , p53 Gene