4.1 Article

Targeting HPV16 DNA using CRISPR/Cas inhibits anal cancer growth in vivo

期刊

FUTURE VIROLOGY
卷 13, 期 7, 页码 475-482

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FUTURE MEDICINE LTD
DOI: 10.2217/fvl-2018-0010

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adeno-associated virus vectors; anal tumors; CRISPR/Cas; gene therapy; human papillomavirus

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资金

  1. National Cancer Institute [R21-CA198050]

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Aim: The goal of this study was to determine if a single AAV vector, encoding Cas9 and guide RNAs specific for the HPV16 E6 and E7 genes, could inhibit the growth of an HPV16-induced tumor in vivo. Materials & methods: We grew HPV16(+), patient-derived anal cancer explants in immunodeficient mice and then challenged these by injection of AAV-based vectors encoding Cas9 and control or HPV16-specific guide RNAs. Results & conclusion: We observed a significant and selective reduction in tumor growth when the HPV16 E6 and E7 genes were targeted using Cas9. These studies provide proof of principle for the hypothesis that CRISPR/Cas has the potential to be used to selectively treat HPV-induced tumors in humans.

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