Journal article
PHLDA1 expression marks the putative epithelial stem cells and contributes to intestinal tumorigenesis
A Sakthianandeswaren, M Christie, C D'Andreti, C Tsui, RN Jorissen, S Li, NI Fleming, P Gibbs, L Lipton, J Malaterre, RG Ramsay, TJ Phesse, M Ernst, RE Jeffery, R Poulsom, SJ Leedham, S Segditsas, IPM Tomlinson, OK Bernhard, RJ Simpson Show all
Cancer Research | AMER ASSOC CANCER RESEARCH | Published : 2011
Abstract
Studies employing mouse models have identified crypt base and position +4 cells as strong candidates for intestinal epithelial stem cells. Equivalent cell populations are thought to exist in the human intestine; however robust and specific protein markers are lacking. Here, we show that in the human small and large intestine, PHLDA1 is expressed in discrete crypt base and some position +4 cells. In small adenomas, PHLDA1 was expressed in a subset of undifferentiated and predominantly Ki-67-negative neoplastic cells, suggesting that a basic hierarchy of differentiation is retained in early tumorigenesis. In large adenomas, carcinomas, and metastases PHLDA1 expression became widespread, with i..
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Grants
Awarded by Medical Research Council
Funding Acknowledgements
This work was supported by the Hilton Ludwig Cancer Metastasis Initiative (L. Lipton, P. Gibbs, and O. M. Sieber), the Victorian Government through a Victorian Cancer Agency Clinical Researcher Fellowship (L. Lipton), Cancer Council Victoria through a Postgraduate Cancer Research Scholarship (M. Christie.), the National Health and Medical Research Council through Program Grant 487922 (J. Malaterre, R. G. Ramsay, T. J. Phesse, M. Ernst, R. J. Simpson, and M. C. Faux) and Project Grant 566679 (E. Vincan). M. Ernst is a senior research fellow of the NHMRC.