4.7 Editorial Material

Modelling intestinal inflammation and infection using 'mini-gut' organoids

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NATURE RESEARCH
DOI: 10.1038/s41575-020-00391-4

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  1. Francis Crick Institute from Cancer Research UK [FC001105]
  2. UK Medical Research Council [FC001105]
  3. Wellcome Trust [FC001105]

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In 2020, major progress has been made in understanding gastrointestinal inflammatory and infectious diseases through the use of 'mini-gut' organoids, including the discovery of somatic inflammatory gene mutations in ulcerative colitis epithelium, a unique mutational signature in colorectal cancer caused by genotoxic Escherichia coli, and the infection of intestinal organoids by SARS-CoV-2.
In 2020, major advances to the understanding of gastrointestinal inflammatory and infectious disease have been made using 'mini-gut' organoids. Key findings include the discovery of somatic inflammatory gene mutations in ulcerative colitis epithelium, a unique mutational signature in colorectal cancer caused by genotoxic Escherichia coli, and infection of intestinal organoids by SARS-CoV-2. Key advances Evolution of somatic inflammatory gene mutations targeting IL-17 signalling occurs during chronic tissue inflammation in patients with ulcerative colitis3. A distinct mutational signature caused by exposure to genotoxic colibactin-producing + is found in a subset of colorectal cancers5. pksEscherichia coliActive SARS-CoV-2 infection and replication is possible in human and bat intestinal organoids7.

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