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LncRNA HOXA11-AS promotes cell growth by sponging miR-24-3p to regulate JPT1 in prostate cancer.

AbstractOBJECTIVE:
Long noncoding RNA (lncRNA) was found to play crucial roles in regulating cancer progression. HOXA11 antisense RNA (HOXA11-AS) was reported to serve an oncogenic lncRNA in cancers but its role in prostate cancer (PCa) remains to be explored.
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.
AuthorsY Cheng, H-Y Xiong, Y-M Li, H-R Zuo, Y Liu, G-L Liao
JournalEuropean 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
PMID34337714 (Publication Type: Journal Article)
Chemical References
  • Cell Cycle Proteins
  • JPT1 protein, human
  • MIRN24 microRNA, human
  • MicroRNAs
  • Microtubule-Associated Proteins
  • RNA, Long Noncoding
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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