ZHX2 restricts hepatocellular carcinoma by suppressing stem cell-like traits through KDM2A-mediated H3K36 demethylation

被引:46
作者
Lin, Qinghai [1 ]
Wu, Zhuanchang [1 ]
Yue, Xuetian [1 ]
Yu, Xiangguo [1 ]
Wang, Zehua [1 ]
Song, Xiaojia [1 ]
Xu, Leiqi [1 ,4 ]
He, Ying [1 ,5 ]
Ge, Yutong [1 ]
Tan, Siyu [1 ]
Wang, Tixiao [1 ]
Song, Hui [1 ]
Yuan, Detian [3 ]
Gong, Yaoqin [1 ,2 ]
Gao, Lifen [1 ]
Liang, Xiaohong [1 ]
Ma, Chunhong [1 ,6 ]
机构
[1] Shandong Univ, Dept Immunol, Minist Educ, Key Lab Expt Teratol,Sch Basic Med Sci, 44 Wenhua Xi Rd, Jinan 250012, Shandong, Peoples R China
[2] Shandong Univ, Sch Basic Med Sci, Dept Mol Med & Genet, Jinan, Shandong, Peoples R China
[3] Shandong Univ, Dept Biochem & Mol Biol, Sch Basic Med Sci, Jinan, Shandong, Peoples R China
[4] Shandong Univ, Dept Gastroenterol, Qilu Hosp, Jinan, Shandong, Peoples R China
[5] Shandong Univ, Inst Basic Med Sci, Qilu Hosp, Jinan, Shandong, Peoples R China
[6] Shandong Univ, Adv Med Res Inst, Jinan, Shandong, Peoples R China
来源
EBIOMEDICINE | 2020年 / 53卷
基金
美国国家科学基金会;
关键词
ZHX2; Tumor suppressor; Epigenetics; Cancer stem cells; Oncotherapy; ALPHA-FETOPROTEIN; CANCER; LIVER; EXPRESSION; IDENTIFICATION; ACTIVATION; RECRUIT;
D O I
10.1016/j.ebiom.2020.102676
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Liver cancer stem cells (CSCs) are critical determinants of HCC relapse and therapeutic resistance, but the mechanisms underlying the maintenance of CSCs are poorly understood. We aimed to explore the role of tumor repressor Zinc-fingers and homeoboxes 2 (ZHX2) in liver CSCs. Methods: CD133(+) or EPCAM(+) stem-like liver cancer cells were sorted from tumor tissues of HCC patients and HCC cell lines by flow cytometry. In addition, sorafenib-resistant cells, tumor-sphere forming cells and side population (SP) cells were respectively cultured and isolated as hepatic CSCs. The tumor-initiating and chemoresistance properties of ZHX2-overexpressing and ZHX2-knockdown cells were analyzed in vivo and in vitro. Microarray, luciferase reporter assay, chromatin immunoprecipitation (ChIP) and ChIP-on-chip analyses were performed to explore ZHX2 target genes. The expression of ZHX2 and its target gene were determined by quantitative RT-PCR, western blot, immunofluorescence and immunohistochemical staining in hepatoma cells and tumor and adjacent tissues from HCC patients. Results: ZHX2 expression was significantly reduced in liver CSCs from different origins. ZHX2 deficiency led to enhanced liver tumor progression and expansion of CSC populations in vitro and in vivo. Re-expression of ZHX2 restricted capabilities of hepatic CSCs in supporting tumor initiation, self-renewal and sorafenib-resistance. Mechanically, ZHX2 suppressed liver CSCs via inhibiting KDM2A-mediated demethylation of histone H3 lysine 36 (H3K36) at the promoter regions of stemness-associated transcription factors, such as NANOG, SOX4 and OCT4. Moreover, patients with lower expression of ZHX2 and higher expression of KDM2A in tumor tissues showed significantly poorer survival. Conclusion: ZHX2 counteracts stem cell traits through transcriptionally repressing KDM2A in HCC. Our data will aid in a better understanding of molecular mechanisms underlying HCC relapse and drug resistance. (c) 2020 The Author(s). Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license. (http://creativecommons.org/licenses/by-nc-nd/4.0/)
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页数:12
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