Literature DB >> 24855947

An essential mesenchymal function for miR-143/145 in intestinal epithelial regeneration.

Raghu R Chivukula1, Guanglu Shi2, Asha Acharya2, Eric W Mills1, Lauren R Zeitels1, Joselin L Anandam3, Abier A Abdelnaby3, Glen C Balch3, John C Mansour3, Adam C Yopp3, Anirban Maitra4, Joshua T Mendell5.   

Abstract

Downregulation of the miR-143/145 microRNA (miRNA) cluster has been repeatedly reported in colon cancer and other epithelial tumors. In addition, overexpression of these miRNAs inhibits tumorigenesis, leading to broad consensus that they function as cell-autonomous epithelial tumor suppressors. We generated mice with deletion of miR-143/145 to investigate the functions of these miRNAs in intestinal physiology and disease in vivo. Although intestinal development proceeded normally in the absence of these miRNAs, epithelial regeneration after injury was dramatically impaired. Surprisingly, we found that miR-143/145 are expressed and function exclusively within the mesenchymal compartment of intestine. Defective epithelial regeneration in miR-143/145-deficient mice resulted from the dysfunction of smooth muscle and myofibroblasts and was associated with derepression of the miR-143 target Igfbp5, which impaired IGF signaling after epithelial injury. These results provide important insights into the regulation of epithelial wound healing and argue against a cell-autonomous tumor suppressor role for miR-143/145 in colon cancer.
Copyright © 2014 Elsevier Inc. All rights reserved.

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Year:  2014        PMID: 24855947      PMCID: PMC4175516          DOI: 10.1016/j.cell.2014.03.055

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  60 in total

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Authors:  Robin C Friedman; Kyle Kai-How Farh; Christopher B Burge; David P Bartel
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3.  Diagnostic and prognostic microRNAs in stage II colon cancer.

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Journal:  Cancer Res       Date:  2008-08-01       Impact factor: 12.701

4.  IGFBP-4 is an inhibitor of canonical Wnt signalling required for cardiogenesis.

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Journal:  Nature       Date:  2008-06-04       Impact factor: 49.962

5.  Altered expression of miR-21, miR-31, miR-143 and miR-145 is related to clinicopathologic features of colorectal cancer.

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6.  Fgf9 signaling regulates small intestinal elongation and mesenchymal development.

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8.  Identification of stem cells in small intestine and colon by marker gene Lgr5.

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9.  miR-145 and miR-143 regulate smooth muscle cell fate and plasticity.

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10.  Most Caenorhabditis elegans microRNAs are individually not essential for development or viability.

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  98 in total

1.  MiR-143 Targeting TAK1 Attenuates Pancreatic Ductal Adenocarcinoma Progression via MAPK and NF-κB Pathway In Vitro.

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2.  MicroRNA Expression and Correlation with mRNA Levels of Colorectal Cancer-Related Genes.

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5.  Upregulation of miR-197 inhibits cell proliferation by directly targeting IGFBP5 in human uterine leiomyoma cells.

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Review 6.  Structural Foundations of RNA Silencing by Argonaute.

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Journal:  J Mol Biol       Date:  2017-07-27       Impact factor: 5.469

Review 7.  Toward the promise of microRNAs - Enhancing reproducibility and rigor in microRNA research.

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Review 8.  The biological functions of miRNAs: lessons from in vivo studies.

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9.  Intestinal anti-inflammatory effects of probiotics in DNBS-colitis via modulation of gut microbiota and microRNAs.

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10.  Inhibition of SW620 human colon cancer cells by upregulating miRNA-145.

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