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Oncol Rep. 2016 Jan;35(1):334-42. doi: 10.3892/or.2015.4335. Epub 2015 Oct 16.

Icaritin acts synergistically with epirubicin to suppress bladder cancer growth through inhibition of autophagy.

Author information

1
Department of Urinary Surgery of Changzheng Hospital, Second Military Medical University, Huangpu, Sanghai 200003, P.R. China.
2
The Urology Research Center of the Chinese People's Liberation Army, Changzheng Hospital, Second Military Medical University, Huangpu, Shanghai 200003, P.R. China.
3
Navy No. 411 Hospital of PLA, Hongkou, Shanghai 200003, P.R. China.

Abstract

Bladder cancer is one of the most commonly diagnosed urological malignancies. Acquired resistance to chemotherapy is a great barrier for achieving successful treatment of bladder cancer. In the present study, we investigated the effect and mechanisms of icaritin, a flavonol glycoside derived from genus Epimedium, against human bladder cancer cells. It was found that despite the low cytotoxicity in normal human HEK293 cells, icaritin significantly inhibited the proliferation and colony formation of BT5637 and T24 bladder cancer cells time- and dose-dependently compared to the DMSO vehicle control. Moreover, cell viability monitored through mitochondrial membrane potential was inhibited markedly after icaritin treatment. Further investigation indicated that icaritin may inhibit epirubicin (EPI)-induced autophagy, and acted synergistically with EPI to suppress the proliferation of BT5637 and T24 cells. These findings suggest that icaritin may prove to be a novel potent therapeutic agent for the treatment of bladder cancer.

PMID:
26496799
DOI:
10.3892/or.2015.4335
[Indexed for MEDLINE]

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