Kruppel-like factor 8 promotes cancer stem cell-like traits in hepatocellular carcinoma through Wnt/β-catenin signaling

被引:26
|
作者
Shen, Yi-Nan [1 ,2 ]
He, Hai-Guan [1 ]
Shi, Yang [1 ]
Cao, Jian [3 ]
Yuan, Jian-Yong [1 ]
Wang, Zhou-Chong [1 ]
Shi, Chun-Feng [1 ]
Zhu, Nan [1 ]
Wei, Yong-Peng [4 ]
Liu, Fang [1 ]
Huang, Jia-Li [1 ]
Yang, Guang-Shun [1 ]
Lu, Jun-Hua [1 ]
机构
[1] Second Mil Med Univ, Eastern Hepatobiliary Surg Hosp, Dept Hepat Surg 5, Shanghai, Peoples R China
[2] Zhejiang Univ, Affiliated Hosp 2, Sch Med, Dept Hepatobiliary & Pancreat Surg, Hangzhou, Zhejiang, Peoples R China
[3] Third Peoples Hosp Jiujiang, Dept Surg 3, Jiujiang, Jiangxi, Peoples R China
[4] Second Mil Med Univ, Xiangan Inst Hlth Retired Cadres, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
hepatocellular carcinoma; liver cancer stem cells; Kruppel-like factor 8 chemoresistance; prognosis; INVASION; KLF8; IDENTIFICATION; ACTIVATION; SUPPRESSION; METASTASIS; EXPRESSION; PROGNOSIS; CISPLATIN; MIGRATION;
D O I
10.1002/mc.22532
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Kruppel-like factor 8 (KLF8) is highly expressed in hepatocellular carcinoma (HCC) and contributes to tumor initiation and progression by promoting HCC cell proliferation and invasion. However, the role of KLF8 in liver cancer stem cells (LCSCs) is not known. In the current study, we investigated the role of KLF8 in LCSCs to determine if KLF8 is a novel marker of these cells. We found that KLF8 was highly expressed in primary HCC tumors, distant migrated tissues, and LCSCs. Patients with high KLF8 expression had a poor prognosis. KLF8 promoted stem cell-like features through activation of the Wnt/-catenin signaling pathway. Cell apoptosis was significantly increased in HCC cells with knockdown of KLF8 compared with the control cells when treated with the same doses of sorafenib or cisplatin. Taken together, our study shows that KLF8 plays a potent oncogenic role in HCC tumorigenesis by maintaining stem cell-like features through activation of the Wnt/-catenin signaling pathway and promoting chemoresistance. Thus, targeting KLF8 may provide an effective therapeutic approach to suppress tumorigenicity of HCC. (c) 2016 Wiley Periodicals, Inc.
引用
收藏
页码:751 / 760
页数:10
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