The Hippo signaling pathway restricts the oncogenic potential of an intestinal regeneration program

被引:477
作者
Cai, Jing [1 ]
Zhang, Nailing [1 ]
Zheng, Yonggang [1 ]
de Wilde, Roeland F. [2 ]
Maitra, Anirban [2 ]
Pan, Duojia [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Howard Hughes Med Inst, Dept Mol Biol & Genet, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Sol Goldman Pancreat Canc Res Ctr, Dept Pathol, Baltimore, MD 21205 USA
关键词
Hippo signaling; cancer; growth control; mouse; regeneration; ORGAN SIZE CONTROL; CELL-PROLIFERATION; EPITHELIAL-CELLS; YAP; TUMORIGENESIS; COLITIS; CANCER; STAT3; LIVER; DROSOPHILA;
D O I
10.1101/gad.1978810
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Although a developmental role for Hippo signaling in organ size control is well appreciated, how this pathway functions in tissue regeneration is largely unknown. Here we address this issue using a dextran sodium sulfate (DSS)-induced colonic regeneration model. We find that regenerating crypts express elevated Yes-associated protein (YAP) levels. Inactivation of YAP causes no obvious intestinal defects under normal homeostasis, but severely impairs DSS-induced intestinal regeneration. Conversely, hyperactivation of YAP results in widespread early-onset polyp formation following DSS treatment. Thus, the YAP oncoprotein must be exquisitely controlled in tissue regeneration to allow compensatory proliferation and prevent the intrinsic oncogenic potential of a tissue regeneration program.
引用
收藏
页码:2383 / 2388
页数:6
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