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Experimental research of quercetin inhibits proliferation and migration of human cervical cancer cells via inhibiting β-catenin
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DOI   10.11656/j.issn.1672-1519.2019.02.25
Key Words   quercetin;cervical cancer cell;Wnt/β-catenin signaling pathway;cell proliferation;cell migration
Author NameAffiliation
WANG Xiangqing Department of Gynaecology and Obstetrics, 464 Hospital of the PLA, Tianjin 300381, China 
MA Zhenjun Department of Gynaecology and Obstetrics, 464 Hospital of the PLA, Tianjin 300381, China 
BAO Hongyun Department of Gynaecology and Obstetrics, 464 Hospital of the PLA, Tianjin 300381, China 
WANG Ru Department of Gynaecology and Obstetrics, 464 Hospital of the PLA, Tianjin 300381, China 
CHEN Xuelian Department of Gynaecology and Obstetrics, 464 Hospital of the PLA, Tianjin 300381, China 
LIU Zhiyong Department of Pathology, Tianjin Medical University Cancer Institute and Hospital, Tianjin 300060, China 
KONG Fangfang Department of Gynaecology and Obstetrics, 464 Hospital of the PLA, Tianjin 300381, China 
Abstract
    [Objective] To investigate the effects of quercetinon proliferation and migration of human cervical cancer (CC) cells by Wnt/β-catenin signaling pathway and its mechanism and to provide a new gene target in the treatment of CC.[Methods] The research objects were the human CC HeLa cells. After treatment with different concentrations ofquercetin for 24 hours, the proliferation of HeLa cells was detected by CCK-8 test, the horizontal and vertical migration were detected by Transwell and wound scraching assays, the activation of Wnt/β-catenin signaling pathway was detected by β-catenin immunofluorescence assay and TOP-flash luciferase reporter system.[Results] CCK-8 test indicated that the cell proliferation rate of the quercetin group was significantly lower than the control group (P<0.01), and the inhibition of quercetinon proliferation was dose-dependent. The horizontal and vertical migration of Hela cells in the quercetin group was significantly decreased compared to the control group(P<0.01). The β-catenin immunofluorescence was distributed in nuclear and cytoplasm in the control cells, while mainly in the cytoplasm in the quercetin-treated cells. Top Flashluciferase reporter system indicated the Wnt/β-catenin signaling pathway was inhibited in the quercetin-treated cells.[Conclusion] Quercetin may inhibit proliferation and migration of human cervical cancer cells via inhibiting Wnt/β-catenin signaling pathway.

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