Suppr超能文献

抑制蛋白激酶 CK2 的表达和活性可阻断肿瘤细胞的生长。

Inhibition of protein kinase CK2 expression and activity blocks tumor cell growth.

机构信息

Celgene Corporation, 4550 Towne Centre Court, San Diego, CA 92121, USA.

出版信息

Mol Cell Biochem. 2010 Jan;333(1-2):159-67. doi: 10.1007/s11010-009-0216-0. Epub 2009 Jul 21.

Abstract

Protein kinase CK2 (CK2) is a highly conserved and ubiquitous serine/threonine kinase. It is a multifunctional and pleiotropic protein kinase implicated in the regulation of cell proliferation, survival, and differentiation. Deregulation of CK2 is observed in a wide variety of tumors. It has been the focus of intensive research efforts to establish the cause-effect relationship between CK2 and neoplastic growth. Here, we further validate the role of CK2 in cancer cell growth using siRNA approach. We also screened a library of more than 200,000 compounds and identified several molecules, which inhibit CK2 with IC(50) < 1 microM. The binding mode of a representative compound with maize CK2 was determined. In addition, the cellular activity of the compounds was demonstrated by their inhibition of phosphorylation of PTEN Ser370 in HCT116 cells. Treatment of a variety of cancer cell lines with the newly identified CK2 inhibitor significantly blocked cell growth with IC(50)s as low as 300 nM.

摘要

蛋白激酶 CK2(CK2)是一种高度保守且普遍存在的丝氨酸/苏氨酸激酶。它是一种多功能、多效性的蛋白激酶,参与细胞增殖、存活和分化的调节。在各种肿瘤中都观察到 CK2 的失调。它一直是研究人员努力确立 CK2 与肿瘤生长之间因果关系的焦点。在这里,我们使用 siRNA 方法进一步验证 CK2 在癌细胞生长中的作用。我们还筛选了一个包含超过 20 万个化合物的文库,并鉴定出几种抑制 CK2 的分子,其 IC50 值<1μM。确定了一种代表性化合物与玉米 CK2 的结合模式。此外,通过抑制 HCT116 细胞中 PTEN Ser370 的磷酸化来证明化合物的细胞活性。用新鉴定的 CK2 抑制剂处理多种癌细胞系,可显著抑制细胞生长,IC50 低至 300 nM。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验