4.8 Article

The ZNF304-integrin axis protects against anoikis in cancer

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NATURE COMMUNICATIONS
卷 6, 期 -, 页码 -

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NATURE PORTFOLIO
DOI: 10.1038/ncomms8351

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  1. National Institutes of Health/National Cancer Institute [R44GM086937, P50 CA093459, U54 CA151668, P50 CA083639, P50 CA098258, R21 CA180145, UH2TR000943, U54CA96300]
  2. Cancer Prevention Research Institute of Texas [RP120214]

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Ovarian 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.

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