國家衛生研究院 NHRI:Item 3990099045/14207
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    題名: Novel insights into the anti-cancer effects of 3-bromopyruvic acid against castration-resistant prostate cancer
    作者: Yeh, HC;Su, CC;Wu, YH;Lee, CH;Bao, BY;Cheng, WC;Wang, SC;Liu, PL;Chiu, CC;Chuu, CP;Ke, CC;Wu, HE;Chen, YR;Chung, WJ;Huang, SP;Li, CY
    貢獻者: Institute of Cellular and Systems Medicine
    摘要: 3-bromopyruvic acid (3-BP), a small molecule alkylating agent, has been emerged as a glycolytic inhibitor with anticancer activities. However, the effects of 3-BP on the growth and metastasis in prostate cancer have not been well investigated. Here we investigated the anti-cancer effects of 3-BP on prostate cancer in vitro and in vivo. Cell growth, apoptosis, migration, motility, and invasion were examined. The tumor growth ability was determined using a xenograft murine model. Transcriptome analysis using RNA-seq was performed to explore the mechanism of action of 3-BP. Our experimental results showed that 3-BP effectively inhibits prostate cancer cell growth, especially in castration-resistant prostate cancer (CRPC) cells. Moreover, 3-BP induces apoptosis and suppresses cell migration, motility, epithelial-mesenchymal transition (EMT), and invasion in CRPC cells. In addition, 3-BP also attenuates tumor growth in a xenograft murine model. Through transcriptome analysis using RNA-seq, 3-BP significantly regulates the cell cycle pathway and decreases the expression of downstream cycle cycle-associated genes in CRPC cells. The results of cell cycle analysis indicated that 3-BP arrests cell cycle progression at G2/M in CRPC cells. These results suggest that 3-BP has the potential in inhibiting CRPC progression and might be a promising drug for CRPC treatment.
    日期: 2022-05-15
    關聯: European Journal of Pharmacology. 2022 May 15;923:Article number 174929.
    Link to: http://dx.doi.org/10.1016/j.ejphar.2022.174929
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=0014-2999&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000806938300001
    Cited Times(Scopus): https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85127335871
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