首页> 美国卫生研究院文献>Blood >Inhibition of proliferation and survival of diffuse large B-cell lymphoma cells by a small-molecule inhibitor of the ubiquitin-conjugating enzyme Ubc13-Uev1A
【2h】

Inhibition of proliferation and survival of diffuse large B-cell lymphoma cells by a small-molecule inhibitor of the ubiquitin-conjugating enzyme Ubc13-Uev1A

机译:泛素结合酶Ubc13-Uev1A的小分子抑制剂抑制弥漫性大B细胞淋巴瘤细胞的增殖和存活

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

Diffuse large B-cell lymphoma (DLBCL), the most common type of non-Hodgkin lymphoma, remains a partially curable disease. Genetic alterations affecting components of NF-κB signaling pathways occur frequently in DLBCL. Almost all activated B cell–like (ABC) DLBCL, which is the least curable group among the 3 major subtypes of this malignancy, and a substantial fraction of germinal center B cell–like (GCB) DLBCL exhibit constitutive NF-κB pathway activity. It has been demonstrated that ABC-DLBCL cells require such activity for proliferation and survival. Therefore, inhibition of NF-κB activation in DLBCL may provide an efficient and targeted therapy. In screening for small-molecule compounds that may inhibit NF-κB activation in DLBCL cells, we identified a compound, NSC697923, which inhibits the activity of the ubiquitin-conjugating (E2) enzyme Ubc13-Uev1A. NSC697923 impedes the formation of the Ubc13 and ubiquitin thioester conjugate and suppresses constitutive NF-κB activity in ABC-DLBCL cells. Importantly, NSC697923 inhibits the proliferation and survival of ABC-DLBCL cells and GCB-DLBCL cells, suggesting the Ubc13-Uev1A may be crucial for DLBCL growth. Consistently, knockdown of Ubc13 expression also inhibited DLBCL cell survival. The results of the present study indicate that Ubc13-Uev1A may represent a potential therapeutic target in DLBCL. In addition, compound NSC697923 may be exploited for the development of DLBCL therapeutic agents.
机译:弥漫性大B细胞淋巴瘤(DLBCL)是非霍奇金淋巴瘤的最常见类型,仍然可以部分治愈。在DLBCL中,影响NF-κB信号通路成分的遗传改变频繁发生。几乎所有活化的B细胞样(ABC)DLBCL(在该恶性肿瘤的3种主要亚型中都是最难治愈的),而大部分生发中心B细胞样(GCB)DLBCL则表现出本构性NF-κB通路活性。已经证明,ABC-DLBCL细胞需要这种活性才能增殖和存活。因此,抑制DLBCL中的NF-κB活化可提供有效的靶向治疗。在筛选可能抑制DLBCL细胞中NF-κB活化的小分子化合物时,我们鉴定了一种化合物NSC697923,该化合物可抑制泛素结合(E2)酶Ubc13-Uev1A的活性。 NSC697923阻止Ubc13和泛素硫酯共轭物的形成,并抑制ABC-DLBCL细胞的本构NF-κB活性。重要的是,NSC697923抑制ABC-DLBCL细胞和GCB-DLBCL细胞的增殖和存活,这表明Ubc13-Uev1A对DLBCL的生长可能至关重要。一致地,Ubc13表达的敲低也抑制了DLBCL细胞的存活。本研究的结果表明,Ubc13-Uev1A可能代表DLBCL的潜在治疗靶标。另外,化合物NSC697923可用于开发DLBCL治疗剂。

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