Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/163561
Title: CRISPR/Cas9-induced DNA damage enriches for mutations in a p53-linked interactome: implications for CRISPR-based therapies
Authors: Jiang, Long
Ingelshed, Katrine
Shen, Yunbing
Boddul, Sanjaykumar V.
Iyer, Vaishnavi Srinivasan
Kasza, Zsolt
Sedimbi, Saikiran
Lane, David P.
Wermeling, Fredrik
Keywords: Science::Medicine
Issue Date: 2022
Source: Jiang, L., Ingelshed, K., Shen, Y., Boddul, S. V., Iyer, V. S., Kasza, Z., Sedimbi, S., Lane, D. P. & Wermeling, F. (2022). CRISPR/Cas9-induced DNA damage enriches for mutations in a p53-linked interactome: implications for CRISPR-based therapies. Cancer Research, 82(1), 36-45. https://dx.doi.org/10.1158/0008-5472.CAN-21-1692
Journal: Cancer Research 
Abstract: Inactivating p53 mutations are the most abundant genetic alterations found in cancer. Here we show that CRISPR/Cas9-induced double-stranded DNA breaks enrich for cells deficient in p53 and in genes of a core CRISPR-p53 tumor suppressor interactome. Such enrichment could predispose to cancer development and thus pose a challenge for clinical CRISPR use. Transient p53 inhibition could suppress the enrichment of cells with these mutations. The level of DNA damage response induced by an sgRNA influenced the enrichment of p53-deficient cells and could be a relevant parameter in sgRNA design to limit cellular enrichment. Furthermore, a dataset of >800 human cancer cell lines identified additional factors influencing the enrichment of p53-mutated cells, including strong baseline CDKN1A expression as a predictor for an active CRISPR-p53 axis. Taken together, these data provide details about p53 biology in the context of CRISPR-induced DNA damage and identify strategies to enable safer CRISPR use. SIGNIFICANCE: CRISPR-mediated DNA damage enriches for cells with escape mutations in a core CRISPR-p53 interactome, which can be suppressed by transient inhibition of p53.
URI: https://hdl.handle.net/10356/163561
ISSN: 0008-5472
DOI: 10.1158/0008-5472.CAN-21-1692
Schools: School of Physical and Mathematical Sciences 
Rights: © 2021 The Authors. Published by the American Association for Cancer Research. This open access article is distributed under the Creative Commons AttributionNonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) license.
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SPMS Journal Articles

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