Targeting SALL4 by entinostat in lung cancer

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Yong, Kol Jia
Li, Ailing
Ou, Wen-Bin
Hong, Clarice Kit Yee
Tatetsu, Hiro
Yan, Benedict
Qi, Lihua
Yang, Henry
Soo, Ross
Note: Order does not necessarily reflect citation order of authors.
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https://doi.org/10.18632/oncotarget.12251Metadata
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Yong, K. J., A. Li, W. Ou, C. K. Y. Hong, W. Zhao, F. Wang, H. Tatetsu, et al. 2016. “Targeting SALL4 by entinostat in lung cancer.” Oncotarget 7 (46): 75425-75440. doi:10.18632/oncotarget.12251. http://dx.doi.org/10.18632/oncotarget.12251.Abstract
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.Other Sources
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5342750/pdf/Terms of Use
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