Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/2418
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dc.contributor.authorDrakulic, Danijelaen_US
dc.contributor.authorVicentic, Jelena Marjanovicen_US
dc.contributor.authorSchwirtlich, Marijaen_US
dc.contributor.authorTosic, Jelenaen_US
dc.contributor.authorKrstic, Aleksandaren_US
dc.contributor.authorKlajn, Andrijanaen_US
dc.contributor.authorStevanović, Milenaen_US
dc.date.accessioned2019-10-23T21:12:21Z-
dc.date.available2019-10-23T21:12:21Z-
dc.date.issued2015-03-
dc.identifier.issn0001-3765-
dc.identifier.urihttps://biore.bio.bg.ac.rs/handle/123456789/2418-
dc.description.abstract© 2015 Academia Brasileira de Ciencias. All rights reserved. The altered expression of the SOX2 transcription factor is associated with oncogenic or tumor suppressor functions in human cancers. This factor regulates the migration and invasion of different cancer cells. In this study we investigated the effect of constitutive SOX2 overexpression on the migration and adhesion capacity of embryonal teratocarcinoma NT2/D1 cells derived from a metastasis of a human testicular germ cell tumor. We detected that increased SOX2 expression changed the speed, mode and path of cell migration, but not the adhesion ability of NT2/D1 cells. Additionally, we demonstrated that SOX2 overexpression increased the expression of the tumor suppressor protein p53 and the HDM2 oncogene. Our results contribute to the better understanding of the effect of SOX2 on the behavior of tumor cells originating from a human testicular germ cell tumor. Considering that NT2/D1 cells resemble cancer stem cells in many features, our results could contribute to the elucidation of the role of SOX2 in cancer stem cells behavior and the process of metastasis.en_US
dc.language.isoenen_US
dc.relation.ispartofAnais da Academia Brasileira de Cienciasen_US
dc.subjectAdhesionen_US
dc.subjectHDM2en_US
dc.subjectMigrationen_US
dc.subjectP53en_US
dc.subjectSOX2en_US
dc.subjectWound healingen_US
dc.titleThe overexpression of SOX2 affects the migration of human teratocarcinoma cell line NT2/D1en_US
dc.typeArticleen_US
dc.identifier.doi10.1590/0001-3765201520140352-
dc.identifier.pmid25761220-
dc.identifier.scopus2-s2.0-84925950061-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/84925950061-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.fulltextWith Fulltext-
item.grantfulltextrestricted-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptChair of Biochemistry and Molecular Biology-
crisitem.author.orcid0000-0003-4286-7334-
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