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Knockdown of Importin 7 Inhibits Lung Tumorigenesis in K-ras(LA1) Lung Cancer Mice

DC Field Value Language
dc.contributor.authorLee, Ah Young-
dc.contributor.authorKim, Sang Wha-
dc.contributor.authorLee, Somin-
dc.contributor.authorJiang, Hu-Lin-
dc.contributor.authorKim, Sang-Bum-
dc.contributor.authorHong, Seong-Ho-
dc.contributor.authorCho, Myung-Haing-
dc.date.accessioned2021-01-31T08:37:43Z-
dc.date.available2021-01-31T08:37:43Z-
dc.date.created2018-08-31-
dc.date.issued2017-05-
dc.identifier.citationAnticancer Research, Vol.37 No.5, pp.2381-2386-
dc.identifier.issn0250-7005-
dc.identifier.other49189-
dc.identifier.urihttps://hdl.handle.net/10371/172298-
dc.description.abstractBackground/Aim: Lung cancer shows the highest estimated deaths in both males and females in the Unites States. Importin 7 is overexpressed in lung adenocarcinoma tissues. In this study, we aimed to demonstrate the anticancer effect of importin 7 down-regulation, especially in lung cancer. Materials and Methods: Glycerol propoxylate triacrylate spermine (GPT-SPE) is a biocompatible carrier used for aerosol gene delivery. Repeated aerosol delivery of GPT-SPE/shImportin 7 complexes was performed to 10-week-old male K-ras(LA1) mice (a murine lung cancer model) twice a week for 4 weeks (8 times) in a nose-only exposure chamber. Results: Aerosol delivery of GPT-SPE/shImportin 7 inhibits lung cancer in K-ras(LA1) mice compared to control and scramble control groups. Moreover, importin 7-down-regulated stable cell-line demonstrates suppression of proliferation through Akt inhibition and apoptosis. Conclusion: Down-regulation of importin 7 significantly suppresses lung cancer in vitro and in vivo.-
dc.language영어-
dc.publisherInternational Institute of Anticancer Research-
dc.titleKnockdown of Importin 7 Inhibits Lung Tumorigenesis in K-ras(LA1) Lung Cancer Mice-
dc.typeArticle-
dc.contributor.AlternativeAuthor조명행-
dc.identifier.doi10.21873/anticanres.11576-
dc.citation.journaltitleAnticancer Research-
dc.identifier.wosid000402173300026-
dc.identifier.scopusid2-s2.0-85019127927-
dc.citation.endpage2386-
dc.citation.number5-
dc.citation.startpage2381-
dc.citation.volume37-
dc.identifier.sci000402173300026-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorCho, Myung-Haing-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusNUCLEAR TRANSLOCATION-
dc.subject.keywordPlusCELL-PROLIFERATION-
dc.subject.keywordPlusAEROSOL DELIVERY-
dc.subject.keywordPlusGENE-THERAPY-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusC-MYC-
dc.subject.keywordPlusRECEPTOR-
dc.subject.keywordPlusSIGNAL-
dc.subject.keywordPlusH1-
dc.subject.keywordPlusPROTEINS-
dc.subject.keywordAuthorLung cancer-
dc.subject.keywordAuthoraerosol delivery-
dc.subject.keywordAuthorgene therapy-
dc.subject.keywordAuthorimportin 7-
dc.subject.keywordAuthorGPT-SPE-
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  • College of Veterinary Medicine
  • Department of Veterinary Medicine
Research Area Nanotoxicology, Veterinary Toxicology

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