ZNF224, Kruppel like zinc finger protein, induces cell growth and apoptosis-resistance by down-regulation of p21 and p53 via miR-663a

被引:33
作者
Cho, Jin Gu [1 ,2 ]
Park, Seho [3 ]
Lim, Chae Hyun [4 ]
Kim, Hong Sook [2 ]
Song, Seung Yong [5 ]
Roh, Tae-Young [4 ]
Sung, Jong-Hyuk [6 ]
Suh, Wonhee [7 ]
Ham, Seok-Jin [4 ]
Lim, Key-Hwan [2 ]
Park, Sang Gyu [2 ]
机构
[1] CHA Univ, Dept Biomed Sci, Songnam, Gyunggi Do, South Korea
[2] Ajou Univ, Dept Pharm, Coll Pharm, Lab Tracing Gene Funct, Suwon 441749, Gyunggi Do, South Korea
[3] Yonsei Univ, Coll Med, Dept Surg, Seoul, South Korea
[4] Pohang Univ Sci & Technol POSTECH, Div Integrat Biosci & Biotechnol, Pohang, Gyeongbuk, South Korea
[5] Yonsei Univ, Coll Med, Dept Plast & Reconstruct Surg, Seoul, South Korea
[6] Yonsei Univ, Dept Pharm, Coll Pharm, Inchon, South Korea
[7] Chung Ang Univ, Dept Pharm, Coll Pharm, Seoul 156756, South Korea
基金
新加坡国家研究基金会;
关键词
ZNF224; miR-663a; p53; p21; apoptosis; BREAST-CANCER CELLS; LUNG-CANCER; TRANSCRIPTIONAL REPRESSION; FUNCTIONAL INTERACTION; DNA-DAMAGE; EXPRESSION; PROMOTES; FAMILY; PROLIFERATION; KAP-1;
D O I
10.18632/oncotarget.8870
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
ZNF224 is a Kruppel-associated box-containing zinc-finger protein which represses gene transcription by interacting with various co-repressors. However, its consensus DNA sequences and target genes are not fully identified. In this study, we identified and characterized consensus DNA sequences containing 5'-CAGC-3' recognized by ZNF224 through ChIP-sequencing, which further confirmed by ELISA, SPR, qPCR, and luciferase activity assay. ZNF224 increased miR-663a transcription by binding to miR-663a promoter, which in turn binds to 3' UTR of p53 and p21 to decrease their expression. miR-663a antagonist abolished ZNF224-mediated suppression of p21 and p53, resulting in the enhanced apoptosis by CPT. The analyses using human breast ductal carcinoma tissues exhibited that the expression of ZNF224 and miR-663a was increased in cancer compared to non-cancer region. Consequently, ZNF224 increases cell survival and decreases apoptosis by decreasing the expression of p53 and p21 via miR-663a as a transcriptional activator. Taken together, we identified and characterized DNA binding element of ZNF224, and its target genes, miR-663a, which provides a novel insight in the down-regulation of p21 and p53 via miR-663a by ZNF224 in breast cancer.
引用
收藏
页码:31177 / 31190
页数:14
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