| Literature DB >> 32944644 |
Veronica Rendo1, Oana M Enache2, Uri Ben-David3.
Abstract
We investigated the genetic and transcriptional changes associated with Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) associated protein 9 (Cas9) expression in human cancer cell lines. For a subset of cell lines with a wild-type tumor protein TP53 (best known as p53), we detected p53 pathway activation, DNA damage accumulation and emerging p53-inactivating mutations following Cas9 introduction. We discuss the potential implications of our findings in basic and translational research.Entities:
Keywords: CRISPR; Cas9; DNA damage response; TP53 mutation; genome editing; p53 pathway
Year: 2020 PMID: 32944644 PMCID: PMC7469564 DOI: 10.1080/23723556.2020.1789419
Source DB: PubMed Journal: Mol Cell Oncol ISSN: 2372-3556