Abstract | OBJECTIVE: MATERIALS AND METHODS: Expression levels of HOXA11-AS in PCa tissues and cells were analyzed with quantitative Real-Time PCR method. MTT assay, colony formation assay, transwell invasion assay, and flow cytometry assay were conducted to explore the biological roles of HOXA11-AS in PCa. Rescue experiments were conducted to investigate mechanisms of HOXA11-AS in regulating PCa progression. RESULTS: We revealed that HOXA11-AS was upregulated in PCa. Silencing of HOXA11-AS significantly inhibited PCa cell proliferation, colony formation, invasion, and promoted apoptosis in vitro. On the contrary, forcing of HOXA11-AS expression caused opposite effects on cancer cell behaviors. Furthermore, we showed that HOXA11-AS1 serves as a competing endogenous RNA ( ceRNA) to regulate Jupiter microtubule associated homolog 1 (JPT1) via sponging microRNA-24-3p (miR-24-3p). Functionally, the overexpression of miR-24-3p or knockdown of JPT1 could partially reverse the effects of HOXA11-AS overexpression on PCa cell behaviors. CONCLUSIONS: This newly identified HOXA11-AS/miR-24-3p/JPT1 axis may provide novel angle for the better control of PCa.
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Authors | Y Cheng, H-Y Xiong, Y-M Li, H-R Zuo, Y Liu, G-L Liao |
Journal | European review for medical and pharmacological sciences
(Eur Rev Med Pharmacol Sci)
Vol. 25
Issue 14
Pg. 4668-4677
(Jul 2021)
ISSN: 2284-0729 [Electronic] Italy |
PMID | 34337714
(Publication Type: Journal Article)
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Chemical References |
- Cell Cycle Proteins
- JPT1 protein, human
- MIRN24 microRNA, human
- MicroRNAs
- Microtubule-Associated Proteins
- RNA, Long Noncoding
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Topics |
- Cell Cycle Proteins
(genetics, metabolism)
- Cell Proliferation
- Cells, Cultured
- Humans
- Male
- MicroRNAs
(genetics, metabolism)
- Microtubule-Associated Proteins
(genetics, metabolism)
- Prostatic Neoplasms
(metabolism, pathology)
- RNA, Long Noncoding
(genetics, metabolism)
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