Diosmetin suppresses human prostate cancer cell proliferation through the induction of apoptosis and cell cycle arrest

被引:53
作者
Oak, Christine [1 ,2 ]
Khalifa, Ahmad O. [1 ,2 ,3 ]
Isali, Ilaha [1 ,2 ]
Bhaskaran, Natarajan [1 ,2 ]
Walker, Ethan [4 ]
Shukla, Sanjeev [1 ,2 ]
机构
[1] Case Western Reserve Univ, Sch Med, Dept Urol, 10900 Euclid Ave, Cleveland, OH 44106 USA
[2] Univ Hosp Cleveland Med Ctr, Urol Inst, Cleveland, OH 44106 USA
[3] Menoufia Univ, Dept Urol, Menoufia 32519, Egypt
[4] Case Western Reserve Univ, Dept Biomed Engn, Cleveland, OH 44106 USA
关键词
prostate cancer cells; diosmetin; growth inhibition; DEPENDENT KINASE INHIBITOR; FLAVONOID DIOSMETIN; CDK INHIBITORS; HEPG2; CELLS; IN-VIVO; METABOLISM; ACTIVATION; MYC; PROGRESSION; EXPRESSION;
D O I
10.3892/ijo.2018.4407
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Diosmetin, a plant flavonoid, has been shown to exert promising effects on prostate cancer cells as an anti-proliferative and anticancer agent. In this study, using western blot analysis for protein expression and flow cytometry for cell cycle analysis, we determined that the treatment of the LNCaP and PC-3 prostate cancer cells with diosmetin resulted in a marked decrease in cyclin D1, Cdk2 and Cdk4 expression levels (these proteins remain active in the G(0)-G(1) phases of the cell cycle). These changes were accompanied by a decrease in c-Myc and Bcl-2 expression, and by an increase in Bax, p27(Kip1) and FOXO3a protein expression, which suggests the potential modulatory effects of diosmetin on protein transcription. The treatment of prostate cancer cells with diosmetin set in motion an apoptotic machinery by inhibiting X-linked inhibitor of apoptosis (XIAP) and increasing cleaved PARP and cleaved caspase-3 expression levels. On the whole, the findings of this study provide an in-depth analysis of the molecular mechanisms responsible for the regulatory effects of diosmetin on key molecules that perturb the cell cycle to inhibit cell growth, and suggest that diosmetin may prove to be an effective anticancer agent for use in the treatment of prostate cancer in the future.
引用
收藏
页码:835 / 843
页数:9
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