Long non-coding RNA ZFAS1 interacts with miR-150-5p to regulate Sp1 expression and ovarian cancer cell malignancy

被引:83
作者
Xia, Bairong [1 ]
Hou, Yan [2 ]
Chen, Hong [1 ]
Yang, Shanshan [1 ]
Liu, Tianbo [1 ]
Lin, Mei [1 ]
Lou, Ge [1 ]
机构
[1] Harbin Med Univ, Affiliated Tumor Hosp, Dept Gynecol, Harbin, Peoples R China
[2] Harbin Med Univ, Sch Publ Hlth, Dept Biostat, Harbin, Peoples R China
基金
中国国家自然科学基金;
关键词
ovarian cancer; long non-coding RNA; ZFAS1; miR-150-5p; Sp1; HEPATOCELLULAR-CARCINOMA; EPIGENETIC REGULATION; TUMOR-SUPPRESSOR; TARGET; TRANSCRIPTION; CHEMOTHERAPY; METHYLATION; MIGRATION; INVASION; GLIOMA;
D O I
10.18632/oncotarget.14663
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We reported that long non-coding RNA ZFAS1 was upregulated in epithelial ovarian cancer tissues, and was negatively correlated to the overall survival rate of patients with epithelial ovarian cancer in this study. While depletion of ZFAS1 inhibited proliferation, migration, and development of chemoresistance, overexpression of ZFAS1 exhibited an even higher proliferation rate, migration activity, and chemoresistance in epithelial ovarian cancer cell lines. We further found miR-150-5p was a potential target of ZFAS1, which was downregulated in epithelial ovarian cancer tissue. MiR-150-5p subsequently inhibited expression of transcription factor Sp1, as evidence by luciferase assays. Inhibition of miR-150-5p rescued the suppressed proliferation and migration induced by depletion of ZFAS1 in epithelial ovarian cancer cells, at least in part. Taken together, our findings revealed a critical role of ZFAS1/miR-150-5p/Sp1 axis in promoting proliferation rate, migration activity, and development of chemoresistance in epithelial ovarian cancer. And ZFAS1/miR-150-5p may serve as novel markers and therapeutic targets of epithelial ovarian cancer.
引用
收藏
页码:19534 / 19546
页数:13
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