PHLDA1 expression marks the putative epithelial stem cells and contributes to intestinal tumorigenesis

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...

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Main Authors: Sakthianandeswaren, A., Christie, M., D'Andreti, C., Tsui, C., Jorissen, R., Li, S., Fleming, N., Gibbs, P., Lipton, L., Malaterre, J., Ramsay, R., Phesse, T., Ernst, M., Jeffery, R., Poulsom, R., Leedham, S., Segditsas, S., Tomlinson, I., Bernhard, O., Simpson, R., Walker, F., Faux, M., Church, N., Catimel, B., Flanagan, D., Vincan, Elizabeth, Sieber, O.
Format: Journal Article
Published: 2011
Online Access:http://hdl.handle.net/20.500.11937/38391
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author Sakthianandeswaren, A.
Christie, M.
D'Andreti, C.
Tsui, C.
Jorissen, R.
Li, S.
Fleming, N.
Gibbs, P.
Lipton, L.
Malaterre, J.
Ramsay, R.
Phesse, T.
Ernst, M.
Jeffery, R.
Poulsom, R.
Leedham, S.
Segditsas, S.
Tomlinson, I.
Bernhard, O.
Simpson, R.
Walker, F.
Faux, M.
Church, N.
Catimel, B.
Flanagan, D.
Vincan, Elizabeth
Sieber, O.
author_facet Sakthianandeswaren, A.
Christie, M.
D'Andreti, C.
Tsui, C.
Jorissen, R.
Li, S.
Fleming, N.
Gibbs, P.
Lipton, L.
Malaterre, J.
Ramsay, R.
Phesse, T.
Ernst, M.
Jeffery, R.
Poulsom, R.
Leedham, S.
Segditsas, S.
Tomlinson, I.
Bernhard, O.
Simpson, R.
Walker, F.
Faux, M.
Church, N.
Catimel, B.
Flanagan, D.
Vincan, Elizabeth
Sieber, O.
author_sort Sakthianandeswaren, A.
building Curtin Institutional Repository
collection Online Access
description 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 increased expression and nuclear localization at invasive margins. siRNA-mediated suppression of PHLDA1 in colon cancer cells inhibited migration and anchorage-independent growth in vitro and tumor growth in vivo. The integrins ITGA2 and ITGA6 were downregulated in response to PHLDA1 suppression, and accordingly cell adhesion to laminin and collagen was significantly reduced. We conclude that PHLDA1 is a putative epithelial stem cell marker in the human small and large intestine and contributes to migration and proliferation in colon cancer cells. ©2011 AACR.
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spelling curtin-20.500.11937-383912017-09-13T14:15:05Z PHLDA1 expression marks the putative epithelial stem cells and contributes to intestinal tumorigenesis Sakthianandeswaren, A. Christie, M. D'Andreti, C. Tsui, C. Jorissen, R. Li, S. Fleming, N. Gibbs, P. Lipton, L. Malaterre, J. Ramsay, R. Phesse, T. Ernst, M. Jeffery, R. Poulsom, R. Leedham, S. Segditsas, S. Tomlinson, I. Bernhard, O. Simpson, R. Walker, F. Faux, M. Church, N. Catimel, B. Flanagan, D. Vincan, Elizabeth Sieber, O. 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 increased expression and nuclear localization at invasive margins. siRNA-mediated suppression of PHLDA1 in colon cancer cells inhibited migration and anchorage-independent growth in vitro and tumor growth in vivo. The integrins ITGA2 and ITGA6 were downregulated in response to PHLDA1 suppression, and accordingly cell adhesion to laminin and collagen was significantly reduced. We conclude that PHLDA1 is a putative epithelial stem cell marker in the human small and large intestine and contributes to migration and proliferation in colon cancer cells. ©2011 AACR. 2011 Journal Article http://hdl.handle.net/20.500.11937/38391 10.1158/0008-5472.CAN-10-2342 unknown
spellingShingle Sakthianandeswaren, A.
Christie, M.
D'Andreti, C.
Tsui, C.
Jorissen, R.
Li, S.
Fleming, N.
Gibbs, P.
Lipton, L.
Malaterre, J.
Ramsay, R.
Phesse, T.
Ernst, M.
Jeffery, R.
Poulsom, R.
Leedham, S.
Segditsas, S.
Tomlinson, I.
Bernhard, O.
Simpson, R.
Walker, F.
Faux, M.
Church, N.
Catimel, B.
Flanagan, D.
Vincan, Elizabeth
Sieber, O.
PHLDA1 expression marks the putative epithelial stem cells and contributes to intestinal tumorigenesis
title PHLDA1 expression marks the putative epithelial stem cells and contributes to intestinal tumorigenesis
title_full PHLDA1 expression marks the putative epithelial stem cells and contributes to intestinal tumorigenesis
title_fullStr PHLDA1 expression marks the putative epithelial stem cells and contributes to intestinal tumorigenesis
title_full_unstemmed PHLDA1 expression marks the putative epithelial stem cells and contributes to intestinal tumorigenesis
title_short PHLDA1 expression marks the putative epithelial stem cells and contributes to intestinal tumorigenesis
title_sort phlda1 expression marks the putative epithelial stem cells and contributes to intestinal tumorigenesis
url http://hdl.handle.net/20.500.11937/38391