Naringenin inhibits migration of bladder cancer cells through downregulation of AKT and MMP-2

doi:10.3892/mmr.2014.2375

CNU IR > College of Smart Living > Dept. of Senior Service and Health Management > Periodical Articles > Item 310902800/28629

Please use this identifier to cite or link to this item: https://ir.cnu.edu.tw/handle/310902800/28629

Title:	Naringenin inhibits migration of bladder cancer cells through downregulation of AKT and MMP-2
Authors:	Liao, Alex Chien Hwa Kuo, Chia-Cheng Huang, Yei-Chung Yeh, Chi-Wei Hseu, You-Cheng Liu, Jer-Yuh Hsu, Li-Sung
Contributors:	老人服務事業管理系
Keywords:	bladder cancer migration matrix metalloproteinase-2 naringenin
Date:	2014-09
Issue Date:	2015-05-06 21:23:06 (UTC+8)
Publisher:	Spandidos Publ Ltd
Abstract:	Bladder cancer is one of the causes of cancer-related death and has a high mortality rate due to its metastatic ability. Naringenin, a bioactive compound predominantly found in citrus fruits, exhibits several cellular functions, including anti-oxidant, -lipidemia and -cancer abilities. However, the effects of naringenin on bladder cancer cells are yet to be elucidated. The present study investigated the molecular mechanisms underlying the effects of naringenin on the migration of TSGH-8301 bladder cancer cells. Treatment with naringenin at doses ranging between 0 and 300 mu M over a period of 24 h was found to reduce cell viability. Furthermore, zymography and western blot analysis revealed that naringenin reduced the expression of matrix metalloproteinase (MMP)-2 in a dose-dependent manner, and repressed its activity. Naringenin also reduced TSGH-8301 cell migration in a concentration-dependent manner, as evidenced by wound healing and Transwell (R) assays. In addition, naringenin was found to inhibit AKT activity and block the nuclear translocation of nuclear factor x-light-chain-enhancer of activated B cells. In conclusion, the findings of the present study show that naringenin is capable of inhibiting bladder cancer cell migration through the downregulation of the AKT and MMP-2 pathways.
Relation:	Molecular Medicine Reports, v.10 n.3, pp.1531-1536
Appears in Collections:	[Dept. of Senior Service and Health Management] Periodical Articles

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