ChIP-seq and Functional Analysis of the SOX2 Gene in Colorectal Cancers

被引:53
作者
Fang, Xuefeng [1 ,2 ]
Yu, Wei [1 ]
Li, Lisha [1 ]
Shao, Jiaofang [1 ]
Zhao, Na [1 ]
Chen, Qiyun [1 ]
Ye, Zhiyun [3 ]
Lin, Sheng-Cai [3 ]
Zheng, Shu [2 ]
Lin, Biaoyang [1 ,4 ,5 ]
机构
[1] Zhejiang Univ, Syst Biol Div, Zhejiang California Int Nanosyst Inst ZCNI, Hangzhou 310029, Zhejiang, Peoples R China
[2] Zhejiang Univ, Affiliated Hosp 2, Key Lab Canc Prevent & Intervent, China Natl Minist Educ,Canc Inst,Sch Med, Hangzhou 310003, Zhejiang, Peoples R China
[3] Xiamen Univ, Sch Life Sci, Minist Educ Cell Biol & Tumor Cell Engn, Key Lab, Fuzhou, Fujian, Peoples R China
[4] Swedish Med Ctr, Seattle, WA USA
[5] Univ Washington, Dept Urol, Seattle, WA 98195 USA
关键词
PLURIPOTENT STEM-CELLS; FACTOR-I RECEPTOR; COLON-CANCER; REGULATE TRANSCRIPTION; EXPRESSION; OVEREXPRESSION; APOPTOSIS; IDENTIFICATION; CARCINOMA; UPSTREAM;
D O I
10.1089/omi.2010.0053
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
SOX2 is anHMGbox containing transcription factor that has been implicated in various types of cancer, but its role in colorectal cancers (CRC) has not been studied. Here we show that SOX2 is overexpressed in CRC tissues compared with normal adjacent tissues using immunohistochemical staining and RT-PCR. We also observed an increased SOX2 expression in nucleus of colorectal cancer tissues (46%, 14/30 cases vs. 7%, 2/30 adjacent tissues). Furthermore, knockdown of SOX2 in SW620 colorectal cancer cells decreased their growth rates in vitro cell line, and in vivo in xenograft models. ChIP-Seq analysis of SOX2 revealed a consensus sequence of wwTGywTT. An integrated expression profiling and ChIP-seq analysis show that SOX2 is involved in the BMP signaling pathway, steroid metabolic process, histone modifications, and many receptor-mediated signaling pathways such as IGF1R and ITPR2 (Inositol 1,4,5-triphosphate receptor, type 2).
引用
收藏
页码:369 / 384
页数:16
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