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dc.contributor.authorAslan, Burcu
dc.contributor.authorMonroig, Paloma
dc.contributor.authorHsu, Ming-Chuan
dc.contributor.authorPena, Guillermo Armaiz
dc.contributor.authorRodriguez-Aguayo, Cristian
dc.contributor.authorGonzalez-Villasana, Vianey
dc.contributor.authorRupaimoole, Rajesha
dc.contributor.authorNagaraja, Archana Sidalaghatta
dc.contributor.authorMangala, Selanere
dc.contributor.authorHan, Hee-Dong
dc.contributor.authorYuca, Erkan
dc.contributor.authorWu, Sherry Y.
dc.contributor.authorIvan, Cristina
dc.contributor.authorMoss, Tyler J.
dc.contributor.authorRam, Prahlad T.
dc.contributor.authorWang, Huamin
dc.contributor.authorGol-Chambers, Alexandra
dc.contributor.authorOzkayar, Ozgur
dc.contributor.authorKanlikilicer, Pinar
dc.contributor.authorFuentes-Mattei, Enrique
dc.contributor.authorKahraman, Nermin
dc.contributor.authorPradeep, Sunila
dc.contributor.authorOzpolat, Bulent
dc.contributor.authorTucker, Susan
dc.contributor.authorHung, Mien-Chie
dc.contributor.authorBaggerly, Keith
dc.contributor.authorBartholomeusz, Geoffrey
dc.contributor.authorCalin, George
dc.contributor.authorSood, Anil K.
dc.contributor.authorLopez-Berestein, Gabriel
dc.date.accessioned2019-12-12T06:47:22Z
dc.date.available2019-12-12T06:47:22Z
dc.date.issued2015
dc.identifier.issn2041-1723
dc.identifier.urihttps://doi.org/10.1038/ncomms8351
dc.identifier.urihttp://hdl.handle.net/11655/17043
dc.description.abstractOvarian cancer (OC) is a highly metastatic disease, but no effective strategies to target this process are currently available. Here, an integrative computational analysis of the Cancer Genome Atlas OC data set and experimental validation identifies a zinc finger transcription factor ZNF304 associated with OC metastasis. High tumoral ZNF304 expression is associated with poor overall survival in OC patients. Through reverse phase protein array analysis, we demonstrate that ZNF304 promotes multiple proto-oncogenic pathways important for cell survival, migration and invasion. ZNF304 transcriptionally regulates beta 1 integrin, which subsequently regulates Src/focal adhesion kinase and paxillin and prevents anoikis. In vivo delivery of ZNF304 siRNA by a dual assembly nanoparticle leads to sustained gene silencing for 14 days, increased anoikis and reduced tumour growth in orthotopic mouse models of OC. Taken together, ZNF304 is a transcriptional regulator of beta 1 integrin, promotes cancer cell survival and protects against anoikis in OC.
dc.language.isoen
dc.publisherNature Publishing Group
dc.relation.isversionof10.1038/ncomms8351
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectScience & Technology - Other Topics
dc.titleThe Znf304-Integrin Axis Protects Against Anoikis In Cancer
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalNature Communications
dc.contributor.departmentTıbbi Patoloji
dc.identifier.volume6
dc.description.indexWoS
dc.description.indexScopus


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