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intestinal stem cells

Comparative Analysis of Patient-Matched PDOs Revealed a Reduction in OLFM4-Associated Clusters in Metastatic Lesions in Colorectal Cancer

[Stem Cell Reports] Combined bulk transcriptomic and single-cell RNA-sequencing analysis revealed decreased gene expression of markers for differentiated cells in patient-derived organoids derived from metastatic lesions.

Signaling Pathways in Intestinal Homeostasis and Colorectal Cancer: KRAS at Centre Stage

[Cell Communication and Signaling] Scientists summarize the signaling pathways contributing to intestinal cell fates and homeostasis functions, focusing on intestinal stem cell proliferation, cell junction formation, remodeling, hypoxia, the impact of intestinal microbiota, the immune system, inflammation, and metabolism.

MAP3K2-Regulated Intestinal Stromal Cells Define a Distinct Stem Cell Niche

[Nature] To determine the physiological role of MAP3K2-regulated intestinal stromal cells (MRISCs), scientists co-cultured MRISCs with colonic organoids and found that organoid growth was greater than when co-cultured with MRISC-depleted stromal cells

Macrophage-Derived EDA-A2 Inhibits Intestinal Stem Cells by Targeting miR-494/EDA2R/β-Catenin Signaling in Mice

[Communications Biology] In colitis crypts, a notable cytokine–cytokine receptor, miR-494-3p-targeted EDA2R and the ligand EDA-A2, suppressed colonic stemness and epithelial repair by inhibiting β-catenin/c-Myc. In differentiated intestinal epithelial cells, miR-494-3p inhibited macrophage recruitment, M1 activation and EDA-A2 secretion by targeting IKKβ/NF-κB in colitis.

The Role of Farnesoid X Receptor in Metabolic Diseases, and Gastrointestinal and Liver Cancer

[Nature Reviews Gastroenterology & Hepatology] Studies on the role of farnesoid X receptor in metabolic diseases and gastrointestinal and liver cancer are discussed, and the potential for development of targeted drugs are summarized.

New Insights and Enhanced Human Norovirus Cultivation in Human Intestinal Enteroids

[mSphere] Human intestinal stem cell-derived enteroids did not support virus replication from every HuNoV-positive stool sample, which led the authors to test and optimize new medium conditions, identify characteristics of stool samples that allow replication, and evaluate consistency of replication over time.

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