Reprogramming the oncogenic response: SET protein as a potential therapeutic target in cancer

被引:21
|
作者
Hung, Man-Hsin [1 ,2 ]
Chen, Kuen-Feng [3 ]
机构
[1] Taipei Vet Gen Hosp, Dept Oncol, Div Med Oncol, Taipei, Taiwan
[2] Natl Yang Ming Univ, Sch Med, Taipei, Taiwan
[3] Natl Taiwan Univ Hosp, Dept Med Res, 7 Chung Shan S Rd, Taipei, Taiwan
关键词
SET; PP2A; cancer; target therapy; oncoprotein; CELL LUNG-CANCER; TYROSINE KINASE INHIBITORS; ACUTE MYELOID-LEUKEMIA; TUMOR-SUPPRESSOR PP2A; CHRONIC LYMPHOCYTIC-LEUKEMIA; ERLOTINIB-INDUCED APOPTOSIS; HISTONE CHAPERONE ACTIVITY; PHOSPHATASE; 2A; HEPATOCELLULAR-CARCINOMA; METASTASIS SUPPRESSOR;
D O I
10.1080/14728222.2017.1336226
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: 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.
引用
收藏
页码:685 / 694
页数:10
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