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The ZNF304-integrin axis protects against anoikis in cancer

Authors :
Tyler J. Moss
Pinar Kanlikilicer
Mien Chie Hung
Sunila Pradeep
Alexandra Gol-Chambers
Paloma Monroig
Prahlad T. Ram
Nermin Kahraman
Selanere Mangala
Keith Baggerly
Cristina Ivan
Geoffrey Bartholomeusz
Ming Chuan Hsu
George A. Calin
Burcu Aslan
Susan L. Tucker
Archana S. Nagaraja
Anil K. Sood
Guillermo N. Armaiz Pena
Rajesha Rupaimoole
Enrique Fuentes-Mattei
Cristian Rodriguez-Aguayo
Erkan Yuca
Ozgur Ozkayar
Gabriel Lopez-Berestein
Huamin Wang
Vianey Gonzalez-Villasana
Sherry Y. Wu
Hee Dong Han
Bulent Ozpolat
Source :
Nature Communications. 6
Publication Year :
2015
Publisher :
Springer Science and Business Media LLC, 2015.

Abstract

Ovarian cancer is a highly metastatic disease, but no effective strategies to target this metastatic process currently are known. Here, an integrative computational analysis of The Cancer Genome Atlas ovarian cancer dataset coupled with experimental validation identified a novel zinc finger transcription factor ZNF304 as one of the key factors for ovarian cancer metastasis. High tumoral ZNF304 expression was associated with poor overall survival in ovarian cancer patients. Through reverse phase protein array analysis, we demonstrated that ZNF304 promotes multiple proto-oncogenic pathways important for cell survival, migration, and invasion. ZNF304 transcriptionally regulates β1 integrin, which subsequently regulates Src/focal adhesion kinase and paxillin and prevents anoikis. In vivo delivery of ZNF304 siRNA by a novel dual assembly nanoparticle led to sustained gene silencing for 14 days, increased anoikis, and reduced tumor growth in orthotopic mouse models of ovarian cancer. Taken together, ZNF304 is a novel transcriptional regulator of β1 integrin, promotes cancer cell survival, and protects against anoikis in ovarian cancer.

Details

ISSN :
20411723
Volume :
6
Database :
OpenAIRE
Journal :
Nature Communications
Accession number :
edsair.doi.dedup.....6eaf000f646b2a1ff830387ad74c044b
Full Text :
https://doi.org/10.1038/ncomms8351