首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >A tropomyosin-like Meretrix meretrix Linnaeus polypeptide inhibits the proliferation and metastasis of glioma cells via microtubule polymerization and FAK/Akt/MMPs signaling
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A tropomyosin-like Meretrix meretrix Linnaeus polypeptide inhibits the proliferation and metastasis of glioma cells via microtubule polymerization and FAK/Akt/MMPs signaling

机译:类似物质素的Meretrix Meretrix Linnaeus多肽通过微管聚合和FAK / AKT / MMPS信号抑制胶质瘤细胞的增殖和转移

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摘要

Glioblastoma (GBM) represents the most common, aggressive and deadliest primary tumors with poor prognosis as available therapeutic approaches fail to control its aberrant proliferation and high invasiveness. Thus, the therapeutic agents targeting these two characteristics will be more effective. In present study, a novel polypeptide (MM15), which was originally purified from Meretrix meretrix Linnaeus and has been proven to possess potent antitumor activity by our laboratory, was recombinant expressed and identified as a tropomyosin homologous protein. The recombinant polypeptide (re-MM15) could induce the U87 cell cycle arrest in G2/M phase and cell apoptosis by inducing tubulin polymerization. Additionally. re-MM15 displayed the significant inhibition to the migration and invasion of U87 cells through downregulating FAK/Akt/MMPs signaling. Furthermore, the in vivo analysis suggested that re-MM15 significantly blocked tumor growth in U87 xenograft model. Collectively, our results indicated that re-MM15, with anti-GBM properties in vitro and in vivo, has promising potential as a new anticancer candidate for GBM. (C) 2019 Elsevier B.V. All rights reserved.
机译:胶质母细胞瘤(GBM)代表最常见,侵略性和最致命性的主要肿瘤,以可用治疗方法未能控制其异常增殖和高侵袭性。因此,靶向这两个特征的治疗剂将更有效。在目前的研究中,新的多肽(MM15)最初由Meretrix Meretrix Linnaeus纯化,并且已被证明是我们实验室具有有效的抗肿瘤活性,其重组表达并鉴定为具有冠状蛋白质蛋白质的冠状蛋白。重组多肽(RE-MM15)可以通过诱导管蛋白聚合来诱导G2 / M相和细胞凋亡中的U87细胞周期停滞。此外。 RE-MM15通过下调FAK / AKT / MMPS信号显示对U87细胞的迁移和侵袭的显着抑制。此外,体内分析表明,RE-MM15在U87异种移植模型中显着阻断了肿瘤生长。总的来说,我们的结果表明,重新MM15,在体外和体内,具有广阔的潜力作为一种新的抗癌候选GBM抗GBM性能。 (c)2019 Elsevier B.v.保留所有权利。

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