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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
来源:
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.
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页码:75425 / 75440
页数:16
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