| Literature DB >> 27939883 |
Toru Nakata1, Hiromichi Shimizu2, Sayaka Nagata1, Go Ito3, Satoru Fujii1, Kohei Suzuki1, Ami Kawamoto1, Fumiaki Ishibashi1, Reiko Kuno1, Sho Anzai1, Tatsuro Murano1, Tomohiro Mizutani1, Shigeru Oshima1, Kiichiro Tsuchiya1, Tetsuya Nakamura4, Katsuto Hozumi5, Mamoru Watanabe1, Ryuichi Okamoto6.
Abstract
Ligand-dependent activation of Notch signaling is required to maintain the stem-cell niche of normal intestinal epithelium. However, the precise role of Notch signaling in the maintenance of the intestinal tumor stem cell niche and the importance of the RBPJ-independent non-canonical pathway in intestinal tumors remains unknown. Here we show that Notch signaling was activated in LGR5+ve cells of APC-deficient mice intestinal tumors. Accordingly, Notch ligands, including Jag1, Dll1, and Dll4, were expressed in these tumors. In vitro studies using tumor-derived organoids confirmed the intrinsic Notch activity-dependent growth of tumor cells. Surprisingly, the targeted deletion of Jag1 but not RBPJ in LGR5+ve tumor-initiating cells resulted in the silencing of Hes1 expression, disruption of the tumor stem cell niche, and dramatic reduction in the proliferation activity of APC-deficient intestinal tumors in vivo. Thus, our results highlight the importance of ligand-dependent non-canonical Notch signaling in the proliferation and maintenance of the tumor stem cell niche in APC-deficient intestinal adenomas.Entities:
Keywords: APC; Intestinal tumor; Jag1; Notch; RBPJ
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Year: 2016 PMID: 27939883 DOI: 10.1016/j.bbrc.2016.12.031
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575