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miR-451a is downregulated and targets PSMB8 in prostate cancer.

Abstract
Abnormal expression of microRNAs (miRNAs) is frequently occurred in prostate cancer (PCa). This study was aimed to investigate the biological roles of miR-451a in PCa. Quantitative real-time PCR (qRT-PCR) and Western blot were employed to investigate the expression levels of miR-451a and proteasome (prosome, macropain) subunit, beta type, 8 (PSMB8) in PCa cell lines. Luciferase activity reporter assay was used to verify the connection between miR-451a and PSMB8. in vitro functional experiments were performed to measure the effects of miR-451a or PSMB8 on PCa cell proliferation, colony formation ability, cell invasion, and cell apoptosis. miR-451a expression was downregulated, whereas PSMB8 expression was upregulated in PCa cell lines. Luciferase activity reporter assay confirmed the direct connection between miR-451a and PSMB8. Overexpression of miR-451a inhibits PCa cell proliferation, colony formation, cell invasion and promotes cell apoptosis, while the overexpression of PSMB8 caused the opposite effects. Moreover, rescue experiments confirmed PSMB8 was a functional target of miR-451a. In conclusion, this study provides novel insights into the role of miR-451a in PCa, and the results demonstrated miR-451a could inhibit PCa progression by targeting PSMB8.
AuthorsYun Liu, Huan-Zhi Yang, Yong-Jun Jiang, Li-Qi Xu
JournalThe Kaohsiung journal of medical sciences (Kaohsiung J Med Sci) Vol. 36 Issue 7 Pg. 494-500 (Jul 2020) ISSN: 2410-8650 [Electronic] China (Republic : 1949- )
PMID32128987 (Publication Type: Journal Article)
Copyright© 2020 The Authors. The Kaohsiung Journal of Medical Sciences published by John Wiley & Sons Australia on behalf of Kaohsiung Medical University.
Chemical References
  • Antigens, CD
  • CDH1 protein, human
  • CDH2 protein, human
  • Cadherins
  • MIRN451 microRNA, human
  • MicroRNAs
  • Oligoribonucleotides
  • Luciferases
  • LMP7 protein
  • Proteasome Endopeptidase Complex
Topics
  • Antigens, CD (genetics, metabolism)
  • Apoptosis (genetics)
  • Base Pairing
  • Base Sequence
  • Cadherins (genetics, metabolism)
  • Cell Line, Tumor
  • Cell Movement
  • Cell Proliferation
  • Gene Expression Regulation, Neoplastic
  • Genes, Reporter
  • Humans
  • Luciferases (genetics, metabolism)
  • Male
  • MicroRNAs (agonists, antagonists & inhibitors, genetics, metabolism)
  • Molecular Mimicry
  • Oligoribonucleotides (genetics, metabolism)
  • Plasmids (chemistry, metabolism)
  • Prostate (metabolism, pathology)
  • Proteasome Endopeptidase Complex (genetics, metabolism)
  • Signal Transduction

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