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PDZ结合激酶/T-LAK细胞源蛋白激酶是褐藻消失墨角藻岩藻依聚糖预防表皮生长因子诱导的肿瘤细胞转化和结肠癌生长的一个靶点。

PDZ-binding kinase/T-LAK cell-originated protein kinase is a target of the fucoidan from brown alga Fucus evanescens in the prevention of EGF-induced neoplastic cell transformation and colon cancer growth.

作者信息

Vishchuk Olesia S, Sun Huimin, Wang Zhe, Ermakova Svetlana P, Xiao JuanJuan, Lu Tao, Xue PeiPei, Zvyagintseva Tatyana N, Xiong Hua, Shao Chen, Yan Wei, Duan Qiuhong, Zhu Feng

机构信息

Department of Biochemistry and Molecular Biology, School of Basic Medicine, Huazhong University of Science and Technology, Wuhan, Hubei 430030, PR China.

G.B. Elyakov Pacific Institute of Bioorganic Chemistry, Far Eastern Branch of Russian Academy of Sciences, Laboratory of Enzyme Chemistry, 690022 Vladivostok, Russian Federation.

出版信息

Oncotarget. 2016 Apr 5;7(14):18763-73. doi: 10.18632/oncotarget.7708.

Abstract

The fucoidan with high anticancer activity was isolated from brown alga Fucus evanescens. The compound effectively prevented EGF-induced neoplastic cell transformation through inhibition of TOPK/ERK1/2/MSK 1 signaling axis. In vitro studies showed that the fucoidan attenuated mitogen-activated protein kinases downstream signaling in a colon cancer cells with different expression level of TOPK, resulting in growth inhibition. The fucoidan exerts its effects by directly interacting with TOPK kinase in vitro and ex vivo and inhibits its kinase activity. In xenograft animal model, oral administration of the fucoidan suppressed HCT 116 colon tumor growth. The phosphorylation of TOPK downstream signaling molecules in tumor tissues was also inhibited by the fucoidan. Taken together, our findings support the cancer preventive efficacy of the fucoidan through its targeting of TOPK for the prevention of neoplastic cell transformation and progression of colon carcinomas in vitro and ex vivo.

摘要

从褐藻消失墨角藻中分离出具有高抗癌活性的岩藻依聚糖。该化合物通过抑制TOPK/ERK1/2/MSK 1信号轴有效预防表皮生长因子诱导的肿瘤细胞转化。体外研究表明,岩藻依聚糖在具有不同TOPK表达水平的结肠癌细胞中减弱丝裂原活化蛋白激酶下游信号传导,从而导致生长抑制。岩藻依聚糖通过在体外和体内与TOPK激酶直接相互作用发挥其作用,并抑制其激酶活性。在异种移植动物模型中,口服岩藻依聚糖可抑制HCT 116结肠肿瘤生长。岩藻依聚糖还可抑制肿瘤组织中TOPK下游信号分子的磷酸化。综上所述,我们的研究结果支持岩藻依聚糖通过靶向TOPK预防体外和体内肿瘤细胞转化及结肠癌进展的防癌功效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d855/4951327/b1a0b2c3edfd/oncotarget-07-18763-g001.jpg

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