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Determination of Stromal Signatures in Breast Carcinoma

Many soft tissue tumors recapitulate features of normal connective tissue. We hypothesize that different types of fibroblastic tumors are representative of different populations of fibroblastic cells or different activation states of these cells. We examined two tumors with fibroblastic features, so...

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Autores principales: West, Robert B, Nuyten, Dimitry S. A, Subramanian, Subbaya, Nielsen, Torsten O, Corless, Christopher L, Rubin, Brian P, Montgomery, Kelli, Zhu, Shirley, Patel, Rajiv, Hernandez-Boussard, Tina, Goldblum, John R, Brown, Patrick O, van de Vijver, Marc, van de Rijn, Matt
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1088973/
https://www.ncbi.nlm.nih.gov/pubmed/15869330
http://dx.doi.org/10.1371/journal.pbio.0030187
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author West, Robert B
Nuyten, Dimitry S. A
Subramanian, Subbaya
Nielsen, Torsten O
Corless, Christopher L
Rubin, Brian P
Montgomery, Kelli
Zhu, Shirley
Patel, Rajiv
Hernandez-Boussard, Tina
Goldblum, John R
Brown, Patrick O
van de Vijver, Marc
van de Rijn, Matt
author_facet West, Robert B
Nuyten, Dimitry S. A
Subramanian, Subbaya
Nielsen, Torsten O
Corless, Christopher L
Rubin, Brian P
Montgomery, Kelli
Zhu, Shirley
Patel, Rajiv
Hernandez-Boussard, Tina
Goldblum, John R
Brown, Patrick O
van de Vijver, Marc
van de Rijn, Matt
author_sort West, Robert B
collection PubMed
description Many soft tissue tumors recapitulate features of normal connective tissue. We hypothesize that different types of fibroblastic tumors are representative of different populations of fibroblastic cells or different activation states of these cells. We examined two tumors with fibroblastic features, solitary fibrous tumor (SFT) and desmoid-type fibromatosis (DTF), by DNA microarray analysis and found that they have very different expression profiles, including significant differences in their patterns of expression of extracellular matrix genes and growth factors. Using immunohistochemistry and in situ hybridization on a tissue microarray, we found that genes specific for these two tumors have mutually specific expression in the stroma of nonneoplastic tissues. We defined a set of 786 gene spots whose pattern of expression distinguishes SFT from DTF. In an analysis of DNA microarray gene expression data from 295 previously published breast carcinomas, we found that expression of this gene set defined two groups of breast carcinomas with significant differences in overall survival. One of the groups had a favorable outcome and was defined by the expression of DTF genes. The other group of tumors had a poor prognosis and showed variable expression of genes enriched for SFT type. Our findings suggest that the host stromal response varies significantly among carcinomas and that gene expression patterns characteristic of soft tissue tumors can be used to discover new markers for normal connective tissue cells.
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spelling pubmed-10889732005-05-10 Determination of Stromal Signatures in Breast Carcinoma West, Robert B Nuyten, Dimitry S. A Subramanian, Subbaya Nielsen, Torsten O Corless, Christopher L Rubin, Brian P Montgomery, Kelli Zhu, Shirley Patel, Rajiv Hernandez-Boussard, Tina Goldblum, John R Brown, Patrick O van de Vijver, Marc van de Rijn, Matt PLoS Biol Research Article Many soft tissue tumors recapitulate features of normal connective tissue. We hypothesize that different types of fibroblastic tumors are representative of different populations of fibroblastic cells or different activation states of these cells. We examined two tumors with fibroblastic features, solitary fibrous tumor (SFT) and desmoid-type fibromatosis (DTF), by DNA microarray analysis and found that they have very different expression profiles, including significant differences in their patterns of expression of extracellular matrix genes and growth factors. Using immunohistochemistry and in situ hybridization on a tissue microarray, we found that genes specific for these two tumors have mutually specific expression in the stroma of nonneoplastic tissues. We defined a set of 786 gene spots whose pattern of expression distinguishes SFT from DTF. In an analysis of DNA microarray gene expression data from 295 previously published breast carcinomas, we found that expression of this gene set defined two groups of breast carcinomas with significant differences in overall survival. One of the groups had a favorable outcome and was defined by the expression of DTF genes. The other group of tumors had a poor prognosis and showed variable expression of genes enriched for SFT type. Our findings suggest that the host stromal response varies significantly among carcinomas and that gene expression patterns characteristic of soft tissue tumors can be used to discover new markers for normal connective tissue cells. Public Library of Science 2005-06 2005-05-10 /pmc/articles/PMC1088973/ /pubmed/15869330 http://dx.doi.org/10.1371/journal.pbio.0030187 Text en Copyright: © 2005 West et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
West, Robert B
Nuyten, Dimitry S. A
Subramanian, Subbaya
Nielsen, Torsten O
Corless, Christopher L
Rubin, Brian P
Montgomery, Kelli
Zhu, Shirley
Patel, Rajiv
Hernandez-Boussard, Tina
Goldblum, John R
Brown, Patrick O
van de Vijver, Marc
van de Rijn, Matt
Determination of Stromal Signatures in Breast Carcinoma
title Determination of Stromal Signatures in Breast Carcinoma
title_full Determination of Stromal Signatures in Breast Carcinoma
title_fullStr Determination of Stromal Signatures in Breast Carcinoma
title_full_unstemmed Determination of Stromal Signatures in Breast Carcinoma
title_short Determination of Stromal Signatures in Breast Carcinoma
title_sort determination of stromal signatures in breast carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1088973/
https://www.ncbi.nlm.nih.gov/pubmed/15869330
http://dx.doi.org/10.1371/journal.pbio.0030187
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