Kulinski Michal, Achkar Iman W, Haris Mohammad, Dermime Said, Mohammad Ramzi M, Uddin Shahab
a Translational Research Institute, Academic Health System , Hamad Medical Corporation , Doha , Qatar.
b Translational Medicine Research Branch , Sidra Medical and Research Center , Doha , Qatar.
Leuk Lymphoma. 2018 May;59(5):1051-1063. doi: 10.1080/10428194.2017.1359740. Epub 2017 Aug 10.
S-phase kinase-associated protein 2 (SKP2) is a well-studied F-box protein and a critical part of the Skp1-Cul1-Fbox (SCF) E3 ligase complex. It controls cell cycle by regulating the expression level of p27 and p21 through ubiquitination and proteasomal degradation. SKP2-mediated loss of p27Kip1 is associated with poor clinical outcome in various types of cancers including hematological malignancies. It is however well established that SKP2 is an oncogene, and its targeting may be an attractive therapeutic strategy for the management of hematological malignancies. In this article, we have highlighted the recent findings from our group and other investigators regarding the role of SKP2 in the pathogenesis of hematological malignancies.
S期激酶相关蛋白2(SKP2)是一种经过充分研究的F盒蛋白,也是Skp1-Cul1-F盒(SCF)E3连接酶复合体的关键组成部分。它通过泛素化和蛋白酶体降解来调节p27和p21的表达水平,从而控制细胞周期。SKP2介导的p27Kip1缺失与包括血液系统恶性肿瘤在内的多种癌症的不良临床预后相关。然而,众所周知SKP2是一种癌基因,靶向作用于它可能是治疗血液系统恶性肿瘤的一种有吸引力的治疗策略。在本文中,我们重点介绍了我们团队以及其他研究人员关于SKP2在血液系统恶性肿瘤发病机制中的作用的最新研究发现。