Targeting SALL4 by entinostat in lung cancer

被引:32
|
作者
Yong, Kol Jia [1 ]
Li, Ailing [2 ]
Ou, Wen-Bin [2 ,3 ]
Hong, Clarice Kit Yee [1 ]
Zhao, Wenxiu [2 ]
Wang, Fei [2 ]
Tatetsu, Hiro [2 ]
Yan, Benedict [4 ]
Qi, Lihua [1 ]
Fletcher, Jonathan A. [2 ]
Yang, Henry [1 ]
Soo, Ross [1 ]
Tenen, Daniel G. [1 ,5 ]
Chai, Li [2 ]
机构
[1] Natl Univ Singapore, Canc Sci Inst Singapore, Singapore, Singapore
[2] Harvard Med Sch, Dept Pathol, Brigham & Womens Hosp, Boston, MA 02115 USA
[3] Zhejiang Sci Tech Univ, Coll Life Sci, Zhejiang Prov Key Lab Silkworm Bioreactor & Biome, Hangzhou, Zhejiang, Peoples R China
[4] Natl Univ Hlth Syst, Natl Univ Singapore Hosp, Dept Lab Med, Singapore, Singapore
[5] Harvard Stem Cell Inst, Boston, MA USA
基金
英国医学研究理事会; 新加坡国家研究基金会;
关键词
entinostat; HDAC inhibitor; lung cancer; SALL4; GERM-CELL TUMORS; RECEPTOR TYROSINE KINASE; FACTOR-I RECEPTOR; ACQUIRED-RESISTANCE; GEFITINIB; EXPRESSION; MUTATIONS; MARKER; GENES; OVEREXPRESSION;
D O I
10.18632/oncotarget.12251
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The overall survival of lung cancer patients remains dismal despite the availability of targeted therapies. Oncofetal protein SALL4 is a novel cancer target. We herein report that SALL4 was aberrantly expressed in a subset of lung cancer patients with poor survival. SALL4 silencing by RNA interference or SALL4 peptide inhibitor treatment led to impaired lung cancer cell growth. Expression profiling of SALL4-knockdown cells demonstrated that both the EGFR and IGF1R signaling pathways were affected. Connectivity Map analysis revealed the HDAC inhibitor entinostat as a potential drug in treating SALL4-expressing cancers, and this was confirmed in 17 lung cancer cell lines. In summary, we report for the first time that entinostat can target SALL4-positive lung cancer. This lays the foundation for future clinical studies evaluating the therapeutic efficacy of entinostat in SALL4-positive lung cancer patients.
引用
收藏
页码:75425 / 75440
页数:16
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