Home > Publications database > Improved detection of colibactin-induced mutations by genotoxic E. coli in organoids and colorectal cancer. |
Journal Article | DKFZ-2024-00523 |
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2024
Elsevier
New York, NY
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Please use a persistent id in citations: doi:10.1016/j.ccell.2024.02.009
Abstract: Co-culture of intestinal organoids with a colibactin-producing pks+E. coli strain (EcC) revealed mutational signatures also found in colorectal cancer (CRC). E. coli Nissle 1917 (EcN) remains a commonly used probiotic, despite harboring the pks operon and inducing double strand DNA breaks. We determine the mutagenicity of EcN and three CRC-derived pks+E. coli strains with an analytical framework based on sequence characteristic of colibactin-induced mutations. All strains, including EcN, display varying levels of mutagenic activity. Furthermore, a machine learning approach attributing individual mutations to colibactin reveals that patients with colibactin-induced mutations are diagnosed at a younger age and that colibactin can induce a specific APC mutation. These approaches allow the sensitive detection of colibactin-induced mutations in ∼12% of CRC genomes and even in whole exome sequencing data, representing a crucial step toward pinpointing the mutagenic activity of distinct pks+E. coli strains.
Keyword(s): bacteria ; cancer genomics ; colibactin ; colorectal cancer ; genotoxins ; machine learning ; mutagenesis ; mutational signatures ; organoids ; probiotics
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