Zinc finger protein 307 functions as a tumor-suppressor and inhibits cell proliferation by inducing apoptosis in hepatocellular carcinoma

被引:14
|
作者
Liang, Yonghao [1 ]
Li, Qisheng [1 ]
Chen, Keli [1 ]
Ni, Wen [1 ]
Zhan, Zetao [1 ]
Ye, Feng [1 ]
Li, Yiyi [1 ]
Fang, Yuan [1 ]
Zhang, Fengjiao [1 ]
Chen, Longhua [1 ]
Ding, Yi [1 ]
机构
[1] Southern Med Univ, Nanfang Hosp, Dept Radiat Oncol, Guangzhou 510515, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
hepatocellular carcinoma; zinc finger protein 307; CANCER;
D O I
10.3892/or.2017.5868
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Zinc finger protein 307 (ZNF307) is a new Kruppel-associated box zinc-finger protein gene and a member of the zinc-finger family of transcriptional factors. Notably, the role of ZNF307 and its underlying mechanisms involved in hepatocarcinogenesis are poorly investigated. In the present study, we found that the expression of ZNF307 was significantly downregulated in hepatocellular carcinoma (HCC) tissues, compared with that in adjacent non-tumor tissues. In vitro studies further demonstrated that ectopic expression of ZNF307 in HCC cell lines Bel7402 and HCCLM3 significantly reduced cell proliferation, migration and invasive ability. Concordantly, knockdown of ZNF307 increased cell proliferation, migration and invasive ability of HCC cell lines MHCC97L and QGY7701. In vivo functional studies showed that upregulation of ZNF307 expression in Bel7402 cells led to a suppression of tumorigenicity in mice, while knockdown of ZNF307 in MHCC97L cells resulted in reverse. effects. Importantly, flow cytometric analysis showed that ZNF307 overexpression increased the incidence of apoptosis, while ZNF307 knockdown decreased the incidence of apoptosis. Consistently, key regulators in apoptosis, such as caspase-3, BAX and BCL-2 were also regulated by ZNF307. Therefore, our results indicate that ZNF307 may serve as a tumor suppressor and inhibits cell proliferation of HCC via inducing apoptosis.
引用
收藏
页码:2229 / 2236
页数:8
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