hsa_circ_0062019 promotes the proliferation, migration, and invasion of prostate cancer cells via the miR-195-5p/HMGA2 axis

被引:16
|
作者
Wang, Peiyu [1 ,2 ,3 ]
Zhang, Ligang [1 ,2 ,3 ]
Yin, Shuiping [1 ,2 ,3 ]
Xu, Yuchen [1 ,2 ,3 ]
Tai, Sheng [1 ,2 ,3 ]
Zhang, L., I [1 ,2 ,3 ]
Liang, Chaozhao [1 ,2 ,3 ]
机构
[1] Anhui Med Univ, Dept Urol, Affiliated Hosp 1, Hefei 230022, Peoples R China
[2] Anhui Med Univ, Inst Urol, Hefei 230032, Peoples R China
[3] Anhui Med Univ, Anhui Prov Key Lab Genitourinary Dis, Hefei 230032, Peoples R China
基金
中国国家自然科学基金;
关键词
prostate cancer; hsa_circ_0062019; competing endogenous RNA; miR-195-5p; high mobility group AT-hook 2; CIRCULAR RNA; PROGRESSION; MIRNA;
D O I
10.1093/abbs/gmab058
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Circular RNA (circRNA) is a new class of non-coding RNA. It was reported that circRNA involves in the metastasis of cancer. The aim of this study is to explore the role and mechanism of circRNA hsa_circ_0062019 in the development of prostate cancer (PCa). Our results showed that hsa_circ_0062019 was highly expressed in PCa cell lines. Cell Counting Kit-8 assay revealed that upregulation of hsa_circ_0062019 boosted PCa cell proliferation, and silencing of hsa_circ_0062019 inhibited cell proliferation. Meanwhile, transwell assay proved that upregulation of hsa_circ_0062019 facilitated PCa cell invasion and migration, while downregulation of hsa_circ_0062019 inhibited these malignant phenotypes. Furthermore, luciferase reporter assay proved the binding of hsa_circ_0062019 with miR-195-5p and the binding between miR-195-5p and high mobility group AT-hook 2 (HMGA2), suggesting that hsa_circ_0062019 promoted the expression of HMGA2 by sponging miR-195-5p. In addition, our results revealed that the hsa_circ_0062019-induced PCa cell malignant phenotypes were notably reversed by the downregulation of HMGA2. Overall, our study demonstrated that hsa_circ_0062019 promoted PCa cell proliferation, migration, and invasion via upregulation of HMGA2 expression by sponging miR-195-5p. Our study proved a novel molecular mechanism of PCa development and provided a potential target for the treatment of PCa.
引用
收藏
页码:815 / 822
页数:8
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