Six2 is negatively correlated with good prognosis and decreases 5-FU sensitivity via suppressing E-cadherin expression in hepatocellular carcinoma cells

被引:10
作者
Li, Jian-Wang [1 ,2 ]
Huang, Chun-Zhen [2 ]
Li, Jian-Hua [4 ]
Yuan, Jian-Hua [2 ]
Chen, Qiong-Hui [2 ]
Zhang, Wei-Fang [2 ]
Xu, Zhen-Sheng [2 ]
Liu, Ying-Ping [2 ]
Li, Yong [3 ]
Zhan, Mei-Xiao [3 ]
Lu, Li-Gong [1 ,3 ]
机构
[1] Southern Med Univ, 1023 South Shatai Rd, Guangzhou 510515, Guangdong, Peoples R China
[2] Cent S Univ, Xiangya Sch Med, Affiliated Haikou Hosp, Dept Oncol, 43 Renmin Ave, Haikou 570208, Hainan, Peoples R China
[3] Zhuhai Peoples Hosp, Zhuhai Precis Med Ctr, 79 Kangning Rd, Zhuhai 519000, Gongdong, Peoples R China
[4] Fuzhou Peoples Hosp, Dept Gen Surg, Fuzhou 344000, Jiangxi, Peoples R China
关键词
5-FU; E-cadherin; Hepatocellular carcinoma; Methylation; Six2; METASTASIS; KIDNEY;
D O I
10.1016/j.biopha.2018.05.032
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
This work aims to study the roles and related mechanisms of six2 in 5-FU sensitivity of hepatocellular carcinoma (HCC) cells. KM-Plotter analysis showed that HCC patients with higher six2 expression levels had shorter overall survival. Six2 expression was higher in clinical HCC tissues than in normal tissues, and was negatively correlated with E-cadherin expression. Additionally, six2 overexpression decreased the sensitivity of HCC cells to 5-Fu, characterized as attenuating 5-FU-induced cell apoptosis and downregulation of cell viability, and promoted HCC cells stemness. Mechanistically, six2 overexpression repressed E-cadherin expression via stimulating promoter methylation of the E-cadherin. And E-cadherin overexpression rescued six2-induced decrease of 5-FU sensitivity and promotion on HCC cells stemness. Therefore, our results suggest that Six2 is negatively correlated with good prognosis and decreases 5-FU sensitivity via suppressing E-cadherin expression in HCC cells.
引用
收藏
页码:204 / 210
页数:7
相关论文
共 16 条
[11]   Loss-of-function screens of druggable targetome against cancer stem-like cells [J].
Song, Mee ;
Lee, Hani ;
Nam, Myung-Hee ;
Jeong, Euna ;
Kim, Somin ;
Hong, Yourae ;
Kim, Nayoung ;
Yim, Hwa Young ;
Yoo, Young-Ji ;
Kim, Jung Seok ;
Kim, Jin-Seok ;
Cho, Yong-Yeon ;
Mills, Gordon B. ;
Kim, Woo-Young ;
Yoon, Sukjoon .
FASEB JOURNAL, 2017, 31 (02) :625-635
[12]   CYP4Z1 3′UTR represses migration of human breast cancer cells [J].
Wang, Bingyu ;
Zheng, Lufeng ;
Chou, Jinjiang ;
Li, Cheng ;
Zhang, Yan ;
Meng, Xia ;
Xi, Tao .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2016, 478 (02) :900-907
[13]   Polycomb group protein EZH2-mediated E-cadherin repression promotes metastasis of oral tongue squamous cell carcinoma [J].
Wang, Cheng ;
Liu, Xiqiang ;
Chen, Zujian ;
Huang, Hongzhang ;
Jin, Yi ;
Kolokythas, Antonia ;
Wang, Anxun ;
Dai, Yang ;
Wong, David T. W. ;
Zhou, Xiaofeng .
MOLECULAR CARCINOGENESIS, 2013, 52 (03) :229-236
[14]   Homeoprotein Six2 Promotes Breast Cancer Metastasis via Transcriptional and Epigenetic Control of E-Cadherin Expression [J].
Wang, Chu-An ;
Drasin, David ;
Pham, Catherine ;
Jedlicka, Paul ;
Zaberezhnyy, Vadym ;
Guney, Michelle ;
Li, Howard ;
Nemenoff, Raphael ;
Costello, James C. ;
Tan, Aik-Choon ;
Ford, Heide L. .
CANCER RESEARCH, 2014, 74 (24) :7357-7370
[15]   The TET2/E-cadherin/β-catenin regulatory loop confers growth and invasion in hepatocellular carcinoma cells [J].
Yang, Guohua ;
Zeng, Xiang ;
Wang, Mengchuan ;
Wu, Aiguo .
EXPERIMENTAL CELL RESEARCH, 2018, 363 (02) :218-226
[16]   miRNA-129-5p suppresses cell proliferation and invasion in lung cancer by targeting microspherule protein 1, E-cadherin and vimentin [J].
Zhang, Yongzhou ;
An, Jihong ;
Lv, Weiling ;
Lou, Tingting ;
Liu, Yunxin ;
Kang, Wenyi .
ONCOLOGY LETTERS, 2016, 12 (06) :5163-5169