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MicroRNA Detection in Prostate Tumors by Quantitative Real-time PCR qPCR
Published on: May 16, 2012
MicroRNA124 regulate cell growth of prostate cancer cells by targeting iASPP
Jun Chen1, Hengjun Xiao2, Zhansen Huang3
1Laboratory of Nanophotonic Functional Materials and Devices, School of Information and Optoelectronic Science and Engineering, South China Normal University Guangzhou 510006, P. R. China ; Department of Infertility and Sexual Medicine, The Third Affiliated Hospital of Sun Yat-Sen University Guangzhou 510630, P. R. China.
Abstract:
Protein phosphatase 1, regulatory subunit 13 like PPP1R13L, also coined iASPP, was found high expression in prostate cancer tissues and cell lines. In previous research, in vitro and in vivo RNAi mediated by artificial lentiviral shRNAs which proved that suppression of iASPP decrease the proliferation of cancer cells. Endogenous interference RNAs, microRNAs play key roles in cell proliferation by post-transcriptional regulation of gene expression. Natural base pair matched microRNA for iASPP is mir124, which was found high expression in growth factorloss prostate cancer cell lines. In this study we examined effect of mir124 upon iASPP and proliferation of prostate cells in vitro with lentiviral infection and use artificial shRNA as control. In vitro reporter assay confirmed that mir124 binding the 3'UTR of iASPP and suppress mRNA expression. Lentivirus mediated mir124 expression decreased the proliferation and viability of PC3 while endogenous iASPP were knocked down.
Insights
MicroRNA-124 (mir124) targets and suppresses Protein Phosphatase 1, Regulatory Subunit 13 Like (iASPP) expression. This finding reduces prostate cancer cell proliferation and viability, offering a potential therapeutic strategy.
Area of Science:
- Oncology
- Molecular Biology
- Gene Regulation
Background:
- Protein phosphatase 1, regulatory subunit 13 like (PPP1R13L), or iASPP, is highly expressed in prostate cancer.
- Previous studies show iASPP suppression reduces cancer cell proliferation via RNA interference.
- MicroRNAs regulate gene expression post-transcriptionally and are implicated in cell proliferation.
Purpose of the Study:
- To investigate the effect of microRNA-124 (mir124) on iASPP expression and prostate cancer cell proliferation in vitro.
- To confirm the direct interaction between mir124 and iASPP mRNA.
- To evaluate mir124 as a potential therapeutic agent against prostate cancer.
Main Methods:
- In vitro reporter assay to confirm mir124 binding to the 3'UTR of iASPP mRNA.
- Lentiviral infection to express mir124 in PC3 prostate cancer cells.
- Use of artificial shRNA as a control for gene silencing.
Main Results:
- In vitro reporter assays confirmed mir124 directly binds to the 3'UTR of iASPP, suppressing its mRNA expression.
- Lentivirus-mediated mir124 expression significantly decreased the proliferation and viability of PC3 cells.
- Endogenous iASPP levels were effectively knocked down by mir124 expression.
Conclusions:
- MicroRNA-124 effectively targets and downregulates iASPP in prostate cancer cells.
- mir124 demonstrates potential as a therapeutic agent by inhibiting prostate cancer cell proliferation and viability.
- The findings highlight the role of mir124 in regulating iASPP and suggest a novel therapeutic avenue for prostate cancer treatment.
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