【2h】

eEF-2 kinase

机译:eEF-2激酶

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Eukaryotic elongation factor-2 (eEF-2) kinase, also known as calmodulin-dependent protein kinase III, is a unique calcium/calmodulin-dependent enzyme. eEF-2 kinase can act as a negative regulator of protein synthesis and a positive regulator of autophagy under environmental or metabolic stresses. Akt, a key downstream effector of the PI3K signaling pathway that regulates cell survival and proliferation, is an attractive therapeutic target for anticancer treatment. Akt inhibition leads to activation of both apoptosis, type I programmed cell death and autophagy, a cellular degradation process via lysosomal machinery (also termed type II programmed cell death). However, the underlying mechanisms that dictate functional relationship between autophagy and apoptosis in response to Akt inhibition remain to be delineated. Our recent study demonstrated that inhibition of eEF-2 kinase can suppress autophagy but promote apoptosis in tumor cells subjected to Akt inhibition, indicating a role of eEF-2 kinase as a controller in the crosstalk between autophagy and apoptosis. Furthermore, inhibition of eEF-2 kinase can reinforce the efficacy of a novel Akt inhibitor, MK-2206, against human glioma. These findings may help optimize the use of Akt inhibitors in the treatment of cancer and other diseases.
机译:真核延伸因子2(eEF-2)激酶,也称为钙调蛋白依赖性蛋白激酶III,是一种独特的钙/钙调蛋白依赖性酶。在环境或代谢压力下,eEF-2激酶可作为蛋白质合成的负调节剂和自噬的正调节剂。 Akt是调节细胞存活和增殖的PI3K信号传导途径的关键下游效应子,是抗癌治疗的有吸引力的治疗靶标。 Akt抑制导致细胞凋亡,I型程序性细胞死亡和自噬(通过溶酶体机制的细胞降解过程)的激活(也称为II型程序性细胞死亡)。然而,决定响应Akt抑制的自噬和凋亡之间的功能关系的潜在机制仍有待描述。我们最近的研究表明,抑制eEF-2激酶可以抑制自噬,但可以促进受到Akt抑制作用的肿瘤细胞凋亡,这表明eEF-2激酶在自噬和凋亡之间的相互作用中起着控制器的作用。此外,对eEF-2激酶的抑制作用可增强新型Akt抑制剂MK-2206对人神经胶质瘤的功效。这些发现可能有助于优化Akt抑制剂在癌症和其他疾病治疗中的使用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号