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一种新型时相依赖的 CENP-E 抑制剂,具有强大的抗肿瘤活性。

A Novel Time-Dependent CENP-E Inhibitor with Potent Antitumor Activity.

机构信息

Oncology Drug Discovery Unit, Pharmaceutical Research Division, Takeda Pharmaceutical Company Limited, Fujisawa, Japan.

DMPK Research Laboratories, Pharmaceutical Research Division, Takeda Pharmaceutical Company Limited, Fujisawa, Japan.

出版信息

PLoS One. 2015 Dec 9;10(12):e0144675. doi: 10.1371/journal.pone.0144675. eCollection 2015.

Abstract

Centromere-associated protein E (CENP-E) regulates both chromosome congression and the spindle assembly checkpoint (SAC) during mitosis. The loss of CENP-E function causes chromosome misalignment, leading to SAC activation and apoptosis during prolonged mitotic arrest. Here, we describe the biological and antiproliferative activities of a novel small-molecule inhibitor of CENP-E, Compound-A (Cmpd-A). Cmpd-A inhibits the ATPase activity of the CENP-E motor domain, acting as a time-dependent inhibitor with an ATP-competitive-like behavior. Cmpd-A causes chromosome misalignment on the metaphase plate, leading to prolonged mitotic arrest. Treatment with Cmpd-A induces antiproliferation in multiple cancer cell lines. Furthermore, Cmpd-A exhibits antitumor activity in a nude mouse xenograft model, and this antitumor activity is accompanied by the elevation of phosphohistone H3 levels in tumors. These findings demonstrate the potency of the CENP-E inhibitor Cmpd-A and its potential as an anticancer therapeutic agent.

摘要

着丝粒相关蛋白 E(CENP-E)在有丝分裂过程中调节染色体的向心性和纺锤体组装检查点(SAC)。CENP-E 功能的丧失导致染色体错位,导致 SAC 激活和长时间有丝分裂阻滞时的细胞凋亡。在这里,我们描述了一种新型 CENP-E 小分子抑制剂,化合物-A(Cmpd-A)的生物学和抗增殖活性。Cmpd-A 抑制 CENP-E 马达结构域的 ATP 酶活性,作为一种时变抑制剂,具有 ATP 竞争性样行为。Cmpd-A 导致中期板上的染色体错位,导致有丝分裂阻滞延长。用 Cmpd-A 处理可诱导多种癌细胞系的增殖抑制。此外,Cmpd-A 在裸鼠异种移植模型中表现出抗肿瘤活性,并且这种抗肿瘤活性伴随着肿瘤中磷酸组蛋白 H3 水平的升高。这些发现证明了 CENP-E 抑制剂 Cmpd-A 的效力及其作为抗癌治疗剂的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afb9/4674098/2852ab420992/pone.0144675.g001.jpg

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