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- Publisher Website: 10.1002/pmic.201000050
- Scopus: eid_2-s2.0-78649403064
- PMID: 20859956
- WOS: WOS:000284044900015
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Article: Proteomic identification of microRNA-122a target proteins in hepatocellular carcinoma
Title | Proteomic identification of microRNA-122a target proteins in hepatocellular carcinoma |
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Authors | |
Keywords | Cell biology Hepatocellular carcinoma MicroRNA-122a Target protein |
Issue Date | 2010 |
Publisher | Wiley - V C H Verlag GmbH & Co KGaA. The Journal's web site is located at http://www.wiley-vch.de/home/proteomics |
Citation | Proteomics, 2010, v. 10 n. 20, p. 3723-3731 How to Cite? |
Abstract | microRNA-122a (miR-122a) is a liver-specific miRNA that is frequently downregulated in hepatocellular carcinoma (HCC). The exact functional role of miR-122a and its target in HCC remain largely unknown. We developed a lentiviral vector for the expression of pre-miR-122a (Lenti-miR-122a). Lenti-miR-122a inhibited HCC cell growth and induced apoptosis in vitro. We employed proteomic profiling to identify the target proteins of miR-122a. In total, ten proteins with differential expression in HCC cells infected with Lenti-miR-122a were identified. Amongst them, downregulation of peroxiredoxin 2 (PRDXII) by miR-122a was validated by Western blotting. Using bioinformatics analysis, predictable target sites of miR-122a were identified in the 5′-UTR of PRDXII mRNA. Luciferase reporter assay confirmed the regulation of miR-122a on 5′-UTR of PRDXII. In conclusion, PRDXII was identified to be the new target of miR-122a. © 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. |
Persistent Identifier | http://hdl.handle.net/10722/168491 |
ISSN | 2023 Impact Factor: 3.4 2023 SCImago Journal Rankings: 1.011 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Diao, S | en_US |
dc.contributor.author | Zhang, JF | en_US |
dc.contributor.author | Wang, H | en_US |
dc.contributor.author | He, ML | en_US |
dc.contributor.author | Lin, MCM | en_US |
dc.contributor.author | Chen, Y | en_US |
dc.contributor.author | Kung, HF | en_US |
dc.date.accessioned | 2012-10-08T03:19:35Z | - |
dc.date.available | 2012-10-08T03:19:35Z | - |
dc.date.issued | 2010 | en_US |
dc.identifier.citation | Proteomics, 2010, v. 10 n. 20, p. 3723-3731 | en_US |
dc.identifier.issn | 1615-9853 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/168491 | - |
dc.description.abstract | microRNA-122a (miR-122a) is a liver-specific miRNA that is frequently downregulated in hepatocellular carcinoma (HCC). The exact functional role of miR-122a and its target in HCC remain largely unknown. We developed a lentiviral vector for the expression of pre-miR-122a (Lenti-miR-122a). Lenti-miR-122a inhibited HCC cell growth and induced apoptosis in vitro. We employed proteomic profiling to identify the target proteins of miR-122a. In total, ten proteins with differential expression in HCC cells infected with Lenti-miR-122a were identified. Amongst them, downregulation of peroxiredoxin 2 (PRDXII) by miR-122a was validated by Western blotting. Using bioinformatics analysis, predictable target sites of miR-122a were identified in the 5′-UTR of PRDXII mRNA. Luciferase reporter assay confirmed the regulation of miR-122a on 5′-UTR of PRDXII. In conclusion, PRDXII was identified to be the new target of miR-122a. © 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. | en_US |
dc.language | eng | en_US |
dc.publisher | Wiley - V C H Verlag GmbH & Co KGaA. The Journal's web site is located at http://www.wiley-vch.de/home/proteomics | en_US |
dc.relation.ispartof | Proteomics | en_US |
dc.subject | Cell biology | - |
dc.subject | Hepatocellular carcinoma | - |
dc.subject | MicroRNA-122a | - |
dc.subject | Target protein | - |
dc.subject.mesh | Animals | en_US |
dc.subject.mesh | Apoptosis - Genetics | en_US |
dc.subject.mesh | Base Sequence | en_US |
dc.subject.mesh | Carcinoma, Hepatocellular - Genetics - Metabolism - Pathology | en_US |
dc.subject.mesh | Cell Line, Tumor | en_US |
dc.subject.mesh | Gene Expression Regulation, Neoplastic | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Liver Neoplasms - Genetics - Metabolism - Pathology | en_US |
dc.subject.mesh | Micrornas - Genetics - Metabolism | en_US |
dc.subject.mesh | Molecular Sequence Data | en_US |
dc.subject.mesh | Neoplasm Proteins - Genetics - Metabolism | en_US |
dc.subject.mesh | Peroxiredoxins - Genetics - Metabolism | en_US |
dc.subject.mesh | Proteome - Analysis | en_US |
dc.subject.mesh | Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization | en_US |
dc.title | Proteomic identification of microRNA-122a target proteins in hepatocellular carcinoma | en_US |
dc.type | Article | en_US |
dc.identifier.email | Lin, MCM:mcllin@hkucc.hku.hk | en_US |
dc.identifier.authority | Lin, MCM=rp00746 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1002/pmic.201000050 | en_US |
dc.identifier.pmid | 20859956 | - |
dc.identifier.scopus | eid_2-s2.0-78649403064 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-78649403064&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 10 | en_US |
dc.identifier.issue | 20 | en_US |
dc.identifier.spage | 3723 | en_US |
dc.identifier.epage | 3731 | en_US |
dc.identifier.isi | WOS:000284044900015 | - |
dc.publisher.place | Germany | en_US |
dc.identifier.scopusauthorid | Diao, S=8939037300 | en_US |
dc.identifier.scopusauthorid | Zhang, JF=13007942600 | en_US |
dc.identifier.scopusauthorid | Wang, H=7501747965 | en_US |
dc.identifier.scopusauthorid | He, ML=35080389700 | en_US |
dc.identifier.scopusauthorid | Lin, MCM=7404816359 | en_US |
dc.identifier.scopusauthorid | Chen, Y=24075600300 | en_US |
dc.identifier.scopusauthorid | Kung, HF=7402514190 | en_US |
dc.identifier.issnl | 1615-9853 | - |