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Gut 2003;52:1237-1239; doi:10.1136/gut.52.9.1237
Copyright © 2003 BMJ Publishing Group Ltd & British Society of Gastroenterology.
Gut 2003;52:1237-1239
© 2003 by BMJ Publishing Group & British Society of Gastroenterology

COMMENTARY

Cancer

Keeping neuroendocrine cells in check: roles for TGFß, Smads, and menin?

G J Dockray

G J Dockray, Physiological Laboratory, University of Liverpool, Crown St, PO Box 147, Liverpool L69 3BX, UK; g.j.dockray@liverpool.ac.uk


Neuroendocrine tumour cells of the gastroenteropancreatic tract are subject to paracrine and autocrine growth inhibition by transforming growth factor ß which may account for the low cell proliferation of this tumour

The first 150 words of the full text of this article appear below.

The endocrine cells of the gastrointestinal epithelium sense the luminal contents and through secretions at their basolateral side signal both to other epithelial cells and to subepithelial cells, including smooth muscle, neurones, and inflammatory cells.1 Some of the features of these cells are clearly neurone-like and for a time it was thought that during development they might be derived, like enteric neurones, from the neural crest. This now seems unlikely, and instead it is thought that normally they arise from the pluripotent stem cells that also give rise to the other epithelial cell lineages.2 However, in some circumstances at least, these cells appear to have the capacity for proliferation, and in extreme cases this gives rise to tumours that are called "neuroendocrine" as they exhibit some of the features of neurones and endocrine cells. There are many similarities between neuroendocrine tumours of the gastrointestinal tract and pancreas. In general, . . . [Full text of this article]


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Relevant Article

Autocrine growth inhibition by transforming growth factor ß-1 (TGFß-1) in human neuroendocrine tumour cells
A Wimmel, B Wiedenmann, and S Rosewicz
Gut 2003 52: 1308-1316. [Abstract] [Full Text] [PDF]

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