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The ZNF304-integrin axis protects against anoikis in cancer
- 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.
- Subjects :
- medicine.medical_specialty
Integrin beta Chains
Integrin
General Physics and Astronomy
Article
General Biochemistry, Genetics and Molecular Biology
Metastasis
Focal adhesion
Cell Movement
Cell Line, Tumor
Internal medicine
medicine
Humans
Gene silencing
Anoikis
Gene Silencing
Paxillin
Cell Proliferation
Ovarian Neoplasms
Multidisciplinary
biology
Carcinoma
General Chemistry
medicine.disease
Gene Expression Regulation, Neoplastic
Endocrinology
Cancer cell
biology.protein
Cancer research
Female
Transcription Factors
Proto-oncogene tyrosine-protein kinase Src
Subjects
Details
- ISSN :
- 20411723
- Volume :
- 6
- Database :
- OpenAIRE
- Journal :
- Nature Communications
- Accession number :
- edsair.doi.dedup.....6eaf000f646b2a1ff830387ad74c044b
- Full Text :
- https://doi.org/10.1038/ncomms8351