نمایش مختصر رکورد

dc.date.accessioned1399-07-08T18:13:41Zfa_IR
dc.date.accessioned2020-09-29T18:13:41Z
dc.date.available1399-07-08T18:13:41Zfa_IR
dc.date.available2020-09-29T18:13:41Z
dc.date.issued2013-12-01en_US
dc.date.issued1392-09-10fa_IR
dc.identifier.citation(2013). Roles of GST-π and polβ Genes in Chemoresistance of Esophageal Carcinoma Cells. Asian Pacific Journal of Cancer Prevention, 14(12), 7375-7379.en_US
dc.identifier.issn1513-7368
dc.identifier.issn2476-762X
dc.identifier.urihttp://journal.waocp.org/article_28482.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/39166
dc.description.abstractThe main aim of this study was to investigate the roles of GST-π and polβ genes in the chemoresistance ofesophageal carcinoma cells. Eukaryotic expression vectors containing each gene were constructed and transfectedinto EC9706 cells, and the biological effects of the two genes assessed based on a resistance index. We additionallyinvestigated the in vitro and in vivo anti-resistance effects of GST-π and polβ genes using recombinant lentivirusescarrying siRNAs against the two genes. Our results showed that upregulation of GST-π and polβ genes suppresseschemosensitivity of esophageal carcinoma cells to cisplatin, while downregulation of these two genes with RNAitechnology reverses this chemoresistance. Multi-site injection of recombinant lentivirus targeting the GST-πgene into transplanted cDDP tumors effectively reversed their chemoresistant phenotype. However, the sametreatment against the polβ gene did not lead to significant efficacy against chemoresistance.en_US
dc.format.extent634
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherWest Asia Organization for Cancer Prevention (WAOCP)en_US
dc.relation.ispartofAsian Pacific Journal of Cancer Preventionen_US
dc.subjectGST-πen_US
dc.subjectpolβen_US
dc.subjectDrug resistanceen_US
dc.subjectEsophageal carcinomaen_US
dc.subjectRNA interferenceen_US
dc.titleRoles of GST-π and polβ Genes in Chemoresistance of Esophageal Carcinoma Cellsen_US
dc.typeTexten_US
dc.citation.volume14
dc.citation.issue12
dc.citation.spage7375
dc.citation.epage7379


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