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Cell Signal. 2014 Mar;26(3):570-9. doi: 10.1016/j.cellsig.2013.11.032. Epub 2013 Dec 2.

Wnt signaling in adult intestinal stem cells and cancer.

Author information

1
Institute of Molecular Genetics, Academy of Sciences of the Czech Republic, Videnska 1083, 142 20 Prague 4, Czech Republic.
2
Institute of Molecular Genetics, Academy of Sciences of the Czech Republic, Videnska 1083, 142 20 Prague 4, Czech Republic. Electronic address: korinek@img.cas.cz.

Abstract

Signaling initiated by secreted glycoproteins of the Wnt family regulates many aspects of embryonic development and it is involved in homeostasis of adult tissues. In the gastrointestinal (GI) tract the Wnt pathway maintains the self-renewal capacity of epithelial stem cells. The stem cell attributes are conferred by mutual interactions of the stem cell with its local microenvironment, the stem cell niche. The niche ensures that the threshold of Wnt signaling in the stem cell is kept in physiological range. In addition, the Wnt pathway involves various feedback loops that balance the opposing processes of cell proliferation and differentiation. Today, we have compelling evidence that mutations causing aberrant activation of the Wnt pathway promote expansion of undifferentiated progenitors and lead to cancer. The review summarizes recent advances in characterization of adult epithelial stem cells in the gut. We mainly focus on discoveries related to molecular mechanisms regulating the output of the Wnt pathway. Moreover, we present novel experimental approaches utilized to investigate the epithelial cell signaling circuitry in vivo and in vitro. Pivotal aspects of tissue homeostasis are often deduced from studies of tumor cells; therefore, we also discuss some latest results gleaned from the deep genome sequencing studies of human carcinomas of the colon and rectum.

KEYWORDS:

APC; Adenomatous Polyposis Coli; Axin; BMP; CBC; CRC; CSCs; Colorectal cancer; Dickkopf; Dkk; FAP; Familial Adenomatous Polyposis; GI; GSK3; Gut; ISCs; LEF/TCF; LGR; LRCs; LRP; MSI; MSS; Mouse models; Organoids; R-spondin; Rnf43; Rspo; TAZ; Tumor; YAP; Yes-associated protein; Znfr3; axis inhibition protein; beta-transducin repeat containing protein; bone morphogenic protein; cancer stem cells; colorectal carcinoma; crypt base columnar; gastrointestinal; glycogen synthase kinase 3; intestinal stem cells; label-retaining cells; leucine-rich G protein coupled receptor; low density lipoprotein receptor-related protein; lymphoid enhancer-binding factor/T-cell factor; microsatellite instability; microsatellite-stable; ring finger 43; transcriptional co-activator with PDZ-binding motif; zinc and ring finger 3; β-TrCP

PMID:
24308963
DOI:
10.1016/j.cellsig.2013.11.032
[Indexed for MEDLINE]
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