نمایش مختصر رکورد

dc.contributor.authorPang, Tianyunen_US
dc.contributor.authorWang, Senen_US
dc.contributor.authorGao, Minen_US
dc.contributor.authorKang, Haixianen_US
dc.contributor.authorZhao, Yien_US
dc.contributor.authorYao, Yunhongen_US
dc.contributor.authorHu, Xinrongen_US
dc.date.accessioned1399-07-09T08:23:20Zfa_IR
dc.date.accessioned2020-09-30T08:23:21Z
dc.date.available1399-07-09T08:23:20Zfa_IR
dc.date.available2020-09-30T08:23:21Z
dc.date.issued2015-07-01en_US
dc.date.issued1394-04-10fa_IR
dc.date.submitted2015-07-30en_US
dc.date.submitted1394-05-08fa_IR
dc.identifier.citationPang, Tianyun, Wang, Sen, Gao, Min, Kang, Haixian, Zhao, Yi, Yao, Yunhong, Hu, Xinrong. (2015). HPV18 E7 induces the over-transcription of eIF4E gene in cervical cancer. Iranian Journal of Basic Medical Sciences, 18(7), 684-690. doi: 10.22038/ijbms.2015.4651en_US
dc.identifier.issn2008-3866
dc.identifier.issn2008-3874
dc.identifier.urihttps://dx.doi.org/10.22038/ijbms.2015.4651
dc.identifier.urihttp://ijbms.mums.ac.ir/article_4651.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/340482
dc.description.abstract<em>Objective(s):</em>Eukaryotic translation initiation factor 4E (eIF4E) is overexpressed in cervical cancer (CC). However, the molecular mechanisms are unclear. This study aimed to investigate the molecular mechanism of eIF4E gene overexpression in CC. <em>Materials </em><em>and</em><em>Methods:</em>The <em>human papillomavirus</em> (<em>HPV</em>) type 18 E7 and eIF4E mRNAs were measured following knock down or overexpression of E7 gene by RT-PCR and real-time PCR. Cell counting kit-8 assay was used to determine the cell proliferation. Flow cytometry was used to analyze the cell cycle and apoptosis. Transwell system was employed to determine the cell migration. <em>Results:</em>Overexpression of E7 gene increased eIF4E mRNA level by 24.3% (<em>P</em><0.01) in HPV negative <em>C33A </em>cells. Knock down of E7 decreased markedly eIF4E mRNA by 73% (<em>P</em><0.01) in HPV18 positive <em>HeLa </em>cells. Under the state of high expression of E7, 1) up-regulation of eIF4E drastically promoted the cell proliferation, cell cycle and cell migration, and inhibited the cell apoptosis.  2) down-regulation of eIF4E significantly inhibited the cell proliferation, cell cycle and the ability of cell  migration,  and  also  promoted  the  apoptosis  of  cervical  cancer  cells. <em>Conclusion: </em>HPV E7 induced eIF4E gene over transcription which might be a new marker for CC. The finding broadens the understanding of the CC carcinogenesis.en_US
dc.format.extent775
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherMashhad University of Medical Sciencesen_US
dc.relation.ispartofIranian Journal of Basic Medical Sciencesen_US
dc.relation.isversionofhttps://dx.doi.org/10.22038/ijbms.2015.4651
dc.subjectEIF4Een_US
dc.subjectCervical Canceren_US
dc.subjectHPVen_US
dc.titleHPV18 E7 induces the over-transcription of eIF4E gene in cervical canceren_US
dc.typeTexten_US
dc.typeOriginal Articleen_US
dc.contributor.departmentObstetrics and Gynecology Department of the first Affiliated Hospital of Guangdong Medical College, No. 57 Avenue of the people, Zhanjiang, Guangdong Province 524023, PR Chinaen_US
dc.contributor.departmentCancer Institute of Guangdong Medical College, No. 1 Xincheng Road, Dongguan, Guangdong Province 523808, PR Chinaen_US
dc.contributor.departmentCancer Institute of Guangdong Medical College, No. 1 Xincheng Road, Dongguan, Guangdong Province 523808, PR Chinaen_US
dc.contributor.departmentCancer Institute of Guangdong Medical College, No. 1 Xincheng Road, Dongguan, Guangdong Province 523808, PR Chinaen_US
dc.contributor.departmentCancer Institute of Guangdong Medical College, No. 1 Xincheng Road, Dongguan, Guangdong Province 523808, PR Chinaen_US
dc.contributor.departmentPathology Department of Guangdong Medical College, No. 1 Xincheng Road, Dongguan, Guangdong Province 523808, PR Chinaen_US
dc.contributor.departmentCancer Institute of Guangdong Medical College, No. 1 Xincheng Road, Dongguan, Guangdong Province 523808, PR Chinaen_US
dc.citation.volume18
dc.citation.issue7
dc.citation.spage684
dc.citation.epage690


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