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靶向真核延伸因子-2 激酶抑制卵巢癌的生长和腹腔转移。

Targeting eukaryotic elongation factor-2 kinase suppresses the growth and peritoneal metastasis of ovarian cancer.

机构信息

Department of Experimental Therapeutics, The University of Texas-MD Anderson Cancer Center, Houston, TX, 77054, USA.

Department of Experimental Therapeutics, The University of Texas-MD Anderson Cancer Center, Houston, TX, 77054, USA; Department of Pharmacology and Toxicology, Faculty of Pharmacy, Al-Azhar University, Cairo, Egypt.

出版信息

Cell Signal. 2021 May;81:109938. doi: 10.1016/j.cellsig.2021.109938. Epub 2021 Feb 2.

Abstract

Ovarian cancer (OC) is the deadliest gynecological cancer and is currently incurable with standard treatment regimens. Early invasion, intraperitoneal metastasis, and an aggressive course are the hallmarks of OC. The major reason for poor prognosis is a lack of molecular targets and highly effective targeted therapies. Therefore, identification of novel molecular targets and therapeutic strategies is urgently needed to improve OC survival. Herein we report that eukaryotic elongation factor-2 kinase (EF2K) is highly upregulated in primary and drug-resistant OC cells and its expresssion associated with progression free survival TCGA database) and promotes cell proliferation, survival, and invasion. Downregulation of EF2K reduced expression of integrin β1 and cyclin D1 and the activity of the Src, phosphoinositide 3-kinase/AKT, and nuclear factor-κB signaling pathways. Also, in vivo, therapeutic targeting of EF2K by using single-lipid nanoparticles containing siRNA led to substantial inhibition of ovarian tumor growth and peritoneal metastasis in nude mouse models. Furthermore, EF2K inhibition led to robust apoptosis and markedly reduced intratumoral proliferation in vivo in ovarian tumor xenografts and intraperitoneal metastatic models. Collectively, our data suggest for the first time that EF2K plays an important role in OC growth, metastasis, and progression and may serve as a novel therapeutic target in OCs.

摘要

卵巢癌(OC)是致命的妇科癌症,目前用标准治疗方案无法治愈。早期侵袭、腹腔内转移和侵袭性病程是 OC 的特征。预后不良的主要原因是缺乏分子靶点和高效的靶向治疗。因此,迫切需要鉴定新的分子靶点和治疗策略,以提高 OC 的生存率。在此,我们报告真核延伸因子-2 激酶(EF2K)在原发性和耐药 OC 细胞中高度上调,其表达与无进展生存期相关(TCGA 数据库),并促进细胞增殖、存活和侵袭。EF2K 的下调降低了整合素 β1 和细胞周期蛋白 D1 的表达以及Src、磷酸肌醇 3-激酶/AKT 和核因子-κB 信号通路的活性。此外,在体内,使用含有 siRNA 的单脂质纳米颗粒对 EF2K 进行治疗靶向治疗,导致裸鼠模型中卵巢肿瘤生长和腹膜转移的显著抑制。此外,EF2K 抑制导致卵巢肿瘤异种移植和腹腔转移模型中肿瘤内增殖的强烈凋亡和明显减少。总之,我们的数据首次表明 EF2K 在 OC 的生长、转移和进展中起重要作用,并且可能成为 OC 的新治疗靶点。

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