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Suppression of tumor growth in xenograft model mice by programmed cell death 4 gene delivery using folate-PEG-baculovirus

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dc.contributor.authorKim, Y-K-
dc.contributor.authorKwon, J-T-
dc.contributor.authorChoi, J. Y.-
dc.contributor.authorJiang, H-L-
dc.contributor.authorArote, R.-
dc.contributor.authorJere, D.-
dc.contributor.authorJe, Y. H.-
dc.contributor.authorCho, M-H-
dc.contributor.authorCho, C-S-
dc.date.accessioned2021-01-31T08:40:57Z-
dc.date.available2021-01-31T08:40:57Z-
dc.date.created2018-01-10-
dc.date.issued2010-11-
dc.identifier.citationCancer Gene Therapy, Vol.17 No.11, pp.751-760-
dc.identifier.issn0929-1903-
dc.identifier.other14328-
dc.identifier.urihttps://hdl.handle.net/10371/172350-
dc.description.abstractCancer gene therapy using tumor suppressor genes is considered to be an attractive approach for arresting cell growth and inducing apoptosis. Programmed cell death 4 (Pdcd4) is a tumor suppressor gene, which prevents tumorigenesis and tumor progression. To address the issue of whether expression of PDCD4 protein induces apoptosis in cancerous cells, the Pdcd4 gene was delivered using folate-PEG-baculovirus. Folate-PEG-baculovirus containing Pdcd4 gene (F-P-Bac-Pdcd4) was constructed by attachment of F-PEG to the baculovirus surface using chemical modification. The F-P-Bac-Pdcd4 showed enhanced transduction efficiency, efficiently expressed PDCD4 protein, and induced apoptosis in human epidermal carcinoma (KB) cells as compared with an unmodified baculovirus. In a tumor xenograft study, injection of F-P-Bac-Pdcd4 into tumors established from the KB cell line by subcutaneous implantation significantly suppressed tumor growth and induced apoptosis. Thus, this study shows a new baculovirus-mediated tumor suppressor gene delivery system for cancer therapy. Cancer Gene Therapy (2010) 17, 751-760; doi:10.1038/cgt.2010.28; published online 11 June 2010-
dc.language영어-
dc.publisherNature Publishing Group-
dc.titleSuppression of tumor growth in xenograft model mice by programmed cell death 4 gene delivery using folate-PEG-baculovirus-
dc.typeArticle-
dc.contributor.AlternativeAuthor조명행-
dc.identifier.doi10.1038/cgt.2010.28-
dc.citation.journaltitleCancer Gene Therapy-
dc.identifier.wosid000283196300001-
dc.identifier.scopusid2-s2.0-77958110145-
dc.citation.endpage760-
dc.citation.number11-
dc.citation.startpage751-
dc.citation.volume17-
dc.identifier.sci000283196300001-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorJe, Y. H.-
dc.contributor.affiliatedAuthorCho, M-H-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusBCL-2 PROTEIN FAMILY-
dc.subject.keywordPlusCANCER-CELLS-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordPlusVIRAL VECTORS-
dc.subject.keywordPlusDOWN-REGULATION-
dc.subject.keywordPlusTHERAPY-
dc.subject.keywordPlusAPOPTOSIS-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusPDCD4-
dc.subject.keywordPlusVIVO-
dc.subject.keywordAuthorbaculovirus-
dc.subject.keywordAuthorprogrammed cell death 4-
dc.subject.keywordAuthorapoptosis-
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  • College of Veterinary Medicine
  • Department of Veterinary Medicine
Research Area Nanotoxicology, Veterinary Toxicology

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