Hung Man-Hsin, Chen Kuen-Feng
a Division of Medical Oncology, Department of Oncology , Taipei Veterans General Hospital , Taipei , Taiwan.
b School of Medicine , National Yang-Ming University , Taipei , Taiwan.
Expert Opin Ther Targets. 2017 Jul;21(7):685-694. doi: 10.1080/14728222.2017.1336226. Epub 2017 Jun 6.
SET is a multitask oncoprotein that promotes the initiation and progression of cancer. Overexpression of SET has been characterized as being tumor-specific and is associated with adverse clinical outcomes in many different human malignant diseases. Notably, SET has been shown to promote the development of therapeutic resistance in cancer cells. Area covered: In this review, we summarized the currently available evidence relating to the oncogenic roles, biological functions and clinical relevance of SET protein in cancer. The anti-cancer effects of three different SET antagonists undergoing preclinical investigation are also discussed. Expert opinion: Emerging evidence supports the critical role of SET in regulating various different cancer hallmarks. Targeting the SET-associated protein interfaces may be a potential anti-cancer strategy for future development. However, more studies are required to clarify the best strategy to combine SET antagonists with other anti-cancer treatments and to explore possible biomarkers that predict responsiveness.
SET是一种多任务癌蛋白,可促进癌症的发生和发展。SET的过表达具有肿瘤特异性,并且与许多不同人类恶性疾病的不良临床结果相关。值得注意的是,SET已被证明可促进癌细胞产生治疗抗性。涵盖领域:在本综述中,我们总结了目前关于SET蛋白在癌症中的致癌作用、生物学功能和临床相关性的现有证据。还讨论了三种正在进行临床前研究的不同SET拮抗剂的抗癌作用。专家观点:新出现的证据支持SET在调节各种不同癌症特征中的关键作用。靶向与SET相关的蛋白质界面可能是未来发展的一种潜在抗癌策略。然而,需要更多研究来阐明将SET拮抗剂与其他抗癌治疗相结合的最佳策略,并探索可能预测反应性的生物标志物。