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Article: The preclinical activity of the histone deacetylase inhibitor PXD101 (belinostat) in hepatocellular carcinoma cell lines

TitleThe preclinical activity of the histone deacetylase inhibitor PXD101 (belinostat) in hepatocellular carcinoma cell lines
Authors
Issue Date2010
Citation
Investigational New Drugs, 2010, v. 28 n. 2, p. 107-114 How to Cite?
AbstractThe activity of the histone deacetylase inhibitor PXD101 was investigated in three hepatocellular carcinoma (HCC) cell lines. PXD101was found to inhibit cell growth at a dose-dependent manner and induce histone acetylation in PLC/PRF/5, Hep3B and HepG2 cells. In PLC/PRF/5 and Hep3B cells which express hepatitis B-related genes (HBx, HBc and HBc), treatment with PXD101 resulted in apoptosis without a significant effect on viral gene expression. Exposure to PXD101 for up to 48 h had varying effects on the expression of 12 cellular genes with tumor suppressor functions, including p21, SOCS1, CMTM5, RASAL1, DLEC1, SFRP (-1, -2, -4 and -5), ADAMTS (-8 and -9). This study provided the basis for a phase II clinical trial of PXD101 in inoperable hepatitis-B associated HCC. © 2009 Springer Science+Business Media, LLC.
Persistent Identifierhttp://hdl.handle.net/10722/194271
ISSN
2015 Impact Factor: 3.281
2015 SCImago Journal Rankings: 1.376
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorMa, BBY-
dc.contributor.authorSung, F-
dc.contributor.authorTao, Q-
dc.contributor.authorPoon, FF-
dc.contributor.authorLui, VW-
dc.contributor.authorYeo, W-
dc.contributor.authorChan, SL-
dc.contributor.authorChan, ATC-
dc.date.accessioned2014-01-30T03:32:23Z-
dc.date.available2014-01-30T03:32:23Z-
dc.date.issued2010-
dc.identifier.citationInvestigational New Drugs, 2010, v. 28 n. 2, p. 107-114-
dc.identifier.issn0167-6997-
dc.identifier.urihttp://hdl.handle.net/10722/194271-
dc.description.abstractThe activity of the histone deacetylase inhibitor PXD101 was investigated in three hepatocellular carcinoma (HCC) cell lines. PXD101was found to inhibit cell growth at a dose-dependent manner and induce histone acetylation in PLC/PRF/5, Hep3B and HepG2 cells. In PLC/PRF/5 and Hep3B cells which express hepatitis B-related genes (HBx, HBc and HBc), treatment with PXD101 resulted in apoptosis without a significant effect on viral gene expression. Exposure to PXD101 for up to 48 h had varying effects on the expression of 12 cellular genes with tumor suppressor functions, including p21, SOCS1, CMTM5, RASAL1, DLEC1, SFRP (-1, -2, -4 and -5), ADAMTS (-8 and -9). This study provided the basis for a phase II clinical trial of PXD101 in inoperable hepatitis-B associated HCC. © 2009 Springer Science+Business Media, LLC.-
dc.languageeng-
dc.relation.ispartofInvestigational New Drugs-
dc.titleThe preclinical activity of the histone deacetylase inhibitor PXD101 (belinostat) in hepatocellular carcinoma cell lines-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1007/s10637-009-9219-7-
dc.identifier.pmid19172229-
dc.identifier.scopuseid_2-s2.0-77952240320-
dc.identifier.volume28-
dc.identifier.issue2-
dc.identifier.spage107-
dc.identifier.epage114-
dc.identifier.isiWOS:000275208300001-

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