Document Detail


Enhanced antitumor efficacy of a novel fiber chimeric oncolytic adenovirus expressing p53 on hepatocellular carcinoma.
MedLine Citation:
PMID:  21504839     Owner:  NLM     Status:  Publisher    
Abstract/OtherAbstract:
Oncolytic adenoviruses may offer a new treatment option and improve the prognosis for patients with hepatocellular carcinoma (HCC). However, the antitumor efficacy of oncolytic adenoviruses on HCC cells is compromised due to low expression of the adenovirus serotype 5 (Ad5) receptor on the target cells. In this study we showed that all HCC cell lines and clinical samples expressed high level of CD46, the receptor for Adenovirus 35 (Ad35) and constructed new fiber chimeric oncolytic adenoviruses with or without a p53 gene expression cassette, SG635-p53 and SG635, respectively. These variants were derived from the previously described Ad5 vectors SG600-p53 and SG600 by replacing the Ad5 fiber with a chimeric Ad5/35 fiber. It was found that the 5/35 fiber chimeric adenovirus vector (Ad5/35-EGFP) demonstrated significantly improved transduction in all tested HCC cell lines compared with the Ad5 vector (Ad5-EGFP). The new fiber chimeric oncolytic adenoviruses produced more progeny viruses in HCC cells than did the Ad5-based viruses but replicated weakly in normal fibroblast BJ cells. In addition, SG635-p53 mediated a higher level of transgenic expression than SG600-p53 in Hep3B and Huh7 cells and showed a markedly enhanced antitumor effect on HCC cells in vitro compared with SG635 or SG600-p53 without causing significant cytotoxicity to normal cells. Antitumor activity of SG635-p53 was shown in Hep3B subcutaneous xenograft tumor models following intratumoral injection, resulting in significant inhibition of tumor growth and prolonged survival of animals. Our data suggest that SG635-p53, as a fiber chimeric oncolytic adenovirus in combination with p53 expression, may serve as a novel, promising and safe anticancer agent for the treatment of HCC.
Authors:
Wei Chen; Yuqiang Wu; Wei Liu; Guoying Wang; Xiaoyun Wang; Yang Yang; Wenjie Chen; Yan Tai; Minqiang Lu; Qijun Qian; Qi Zhang; Guihua Chen
Related Documents :
20696059 - Anti-tumor effects of retinoids combined with trastuzumab or tamoxifen in breast cancer...
20397199 - Inhibitory effects of 5-hydroxy polymethoxyflavones on colon cancer cells.
19177499 - Mtbitc mediates cell cycle arrest and apoptosis induction in human hepg2 cells despite ...
16187279 - A novel role for placental leucine aminopeptidase (p-lap) as a determinant of chemoresi...
8832209 - Subcellular localization of proteasomes in apoptotic lung tumor cells and persistence a...
14572459 - A role of p301l tau mutant in anti-apoptotic gene expression, cell cycle and apoptosis.
21251009 - The descent of memory t cells.
18575829 - Extracellular atp and cancer: an overview with special reference to p2 purinergic recep...
17458629 - Actin-filament-dependent remodeling of the vacuole in cultured mesophyll protoplasts.
Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2011-4-18
Journal Detail:
Title:  Cancer letters     Volume:  -     ISSN:  1872-7980     ISO Abbreviation:  -     Publication Date:  2011 Apr 
Date Detail:
Created Date:  2011-4-20     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  7600053     Medline TA:  Cancer Lett     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
Copyright Information:
Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.
Affiliation:
Liver Transplantation Center, 3rd Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China; Guangdong Provincial Key Laboratory of Liver Disease Research, Guangzhou, China.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Activation of coagulation in amniotic fluid during normal human pregnancy.
Next Document:  Enhancement of psychotherapy using epigenetic modulating drugs.