First evidence supporting a potential role for the BMP/SMAD pathway in the progression of oestrogen receptor-positive breast cancer

Oestrogen receptor expression is generally a sign of better tumour differentiation and comparatively good clinical outcome in invasive breast cancer. However, oestrogen receptor‐positive, poorly differentiated carcinomas with a poor clinical outcome exist. The underlying genetic mechanisms and the g...

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Veröffentlicht in:The Journal of pathology 2005-07, Vol.206 (3), p.366-376
Hauptverfasser: Helms, Mike W, Packeisen, Jens, August, Christian, Schittek, Birgit, Boecker, Werner, Brandt, Burkhard H, Buerger, Horst
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container_start_page 366
container_title The Journal of pathology
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creator Helms, Mike W
Packeisen, Jens
August, Christian
Schittek, Birgit
Boecker, Werner
Brandt, Burkhard H
Buerger, Horst
description Oestrogen receptor expression is generally a sign of better tumour differentiation and comparatively good clinical outcome in invasive breast cancer. However, oestrogen receptor‐positive, poorly differentiated carcinomas with a poor clinical outcome exist. The underlying genetic mechanisms and the genes involved remain obscure, even though chromosome 7p gains seem to be associated with these uncommon tumours. In this study, we compared two subsets of oestrogen receptor‐positive breast cancers, which differed in tumour grade, cytogenetic instability, and tumour proliferation, for their differential gene expression in order to identify proteins involved in the progression of oestrogen receptor‐positive breast cancers. We were able to show by means of subtractive suppression hybridization, real‐time reverse transcriptase PCR, and tissue microarray analysis that expression of the bone morphogenetic protein receptor IB (BMPR‐IB) is a major hallmark of the progression and dedifferentiation of breast cancer. Strong expression of BMPR‐IB was associated with high tumour grade, high tumour proliferation, cytogenetic instability, and a poor prognosis in oestrogen receptor‐positive carcinomas. Western blot analysis revealed that downstream signalling of this receptor is mainly mediated via phosphorylation of SMAD 1 in oestrogen receptor‐positive breast cancer. Even though BMPR‐IB was expressed in oestrogen receptor‐positive and ‐negative breast cancers, an impact on tumour grade, proliferation, and cytogenetic instability, as parameters of tumour progression, could only be demonstrated in oestrogen receptor‐positive carcinomas. This pro‐proliferative effect was complemented by significant anti‐apoptotic activity, indicated by XIAP and IAP‐2 expression in BMPR‐IB‐positive carcinomas. These results show that the BMP/SMAD pathway is activated in breast cancer and may contribute to breast cancer progression and dedifferentiation in oestrogen receptor‐positive breast cancer. The definition of this pathway characterizes a new potential target in the molecular treatment of invasive breast cancer. Copyright © 2005 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
doi_str_mv 10.1002/path.1785
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However, oestrogen receptor‐positive, poorly differentiated carcinomas with a poor clinical outcome exist. The underlying genetic mechanisms and the genes involved remain obscure, even though chromosome 7p gains seem to be associated with these uncommon tumours. In this study, we compared two subsets of oestrogen receptor‐positive breast cancers, which differed in tumour grade, cytogenetic instability, and tumour proliferation, for their differential gene expression in order to identify proteins involved in the progression of oestrogen receptor‐positive breast cancers. We were able to show by means of subtractive suppression hybridization, real‐time reverse transcriptase PCR, and tissue microarray analysis that expression of the bone morphogenetic protein receptor IB (BMPR‐IB) is a major hallmark of the progression and dedifferentiation of breast cancer. Strong expression of BMPR‐IB was associated with high tumour grade, high tumour proliferation, cytogenetic instability, and a poor prognosis in oestrogen receptor‐positive carcinomas. Western blot analysis revealed that downstream signalling of this receptor is mainly mediated via phosphorylation of SMAD 1 in oestrogen receptor‐positive breast cancer. Even though BMPR‐IB was expressed in oestrogen receptor‐positive and ‐negative breast cancers, an impact on tumour grade, proliferation, and cytogenetic instability, as parameters of tumour progression, could only be demonstrated in oestrogen receptor‐positive carcinomas. This pro‐proliferative effect was complemented by significant anti‐apoptotic activity, indicated by XIAP and IAP‐2 expression in BMPR‐IB‐positive carcinomas. These results show that the BMP/SMAD pathway is activated in breast cancer and may contribute to breast cancer progression and dedifferentiation in oestrogen receptor‐positive breast cancer. The definition of this pathway characterizes a new potential target in the molecular treatment of invasive breast cancer. Copyright © 2005 Pathological Society of Great Britain and Ireland. Published by John Wiley &amp; Sons, Ltd.</description><identifier>ISSN: 0022-3417</identifier><identifier>EISSN: 1096-9896</identifier><identifier>DOI: 10.1002/path.1785</identifier><identifier>PMID: 15892165</identifier><identifier>CODEN: JPTLAS</identifier><language>eng</language><publisher>Chichester, UK: John Wiley &amp; Sons, Ltd</publisher><subject>Apoptosis - genetics ; Biological and medical sciences ; Blotting, Western - methods ; BMPR-IB ; Bone Morphogenetic Protein Receptors, Type I ; breast cancer ; Breast Neoplasms - genetics ; Breast Neoplasms - metabolism ; Breast Neoplasms - pathology ; Cell Differentiation - genetics ; CGH ; CXCR4 ; dedifferentiation ; Disease Progression ; DNA-Binding Proteins - genetics ; DNA-Binding Proteins - metabolism ; Female ; Gene Expression Regulation, Neoplastic - genetics ; Humans ; Investigative techniques, diagnostic techniques (general aspects) ; Medical sciences ; Neoplasm Invasiveness ; Neoplasm Proteins - genetics ; Neoplasm Proteins - metabolism ; Nucleic Acid Hybridization - methods ; Oligonucleotide Array Sequence Analysis - methods ; Pathology. 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Pathol</addtitle><description>Oestrogen receptor expression is generally a sign of better tumour differentiation and comparatively good clinical outcome in invasive breast cancer. However, oestrogen receptor‐positive, poorly differentiated carcinomas with a poor clinical outcome exist. The underlying genetic mechanisms and the genes involved remain obscure, even though chromosome 7p gains seem to be associated with these uncommon tumours. In this study, we compared two subsets of oestrogen receptor‐positive breast cancers, which differed in tumour grade, cytogenetic instability, and tumour proliferation, for their differential gene expression in order to identify proteins involved in the progression of oestrogen receptor‐positive breast cancers. We were able to show by means of subtractive suppression hybridization, real‐time reverse transcriptase PCR, and tissue microarray analysis that expression of the bone morphogenetic protein receptor IB (BMPR‐IB) is a major hallmark of the progression and dedifferentiation of breast cancer. Strong expression of BMPR‐IB was associated with high tumour grade, high tumour proliferation, cytogenetic instability, and a poor prognosis in oestrogen receptor‐positive carcinomas. Western blot analysis revealed that downstream signalling of this receptor is mainly mediated via phosphorylation of SMAD 1 in oestrogen receptor‐positive breast cancer. Even though BMPR‐IB was expressed in oestrogen receptor‐positive and ‐negative breast cancers, an impact on tumour grade, proliferation, and cytogenetic instability, as parameters of tumour progression, could only be demonstrated in oestrogen receptor‐positive carcinomas. This pro‐proliferative effect was complemented by significant anti‐apoptotic activity, indicated by XIAP and IAP‐2 expression in BMPR‐IB‐positive carcinomas. These results show that the BMP/SMAD pathway is activated in breast cancer and may contribute to breast cancer progression and dedifferentiation in oestrogen receptor‐positive breast cancer. The definition of this pathway characterizes a new potential target in the molecular treatment of invasive breast cancer. Copyright © 2005 Pathological Society of Great Britain and Ireland. 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Pathol</addtitle><date>2005-07</date><risdate>2005</risdate><volume>206</volume><issue>3</issue><spage>366</spage><epage>376</epage><pages>366-376</pages><issn>0022-3417</issn><eissn>1096-9896</eissn><coden>JPTLAS</coden><abstract>Oestrogen receptor expression is generally a sign of better tumour differentiation and comparatively good clinical outcome in invasive breast cancer. However, oestrogen receptor‐positive, poorly differentiated carcinomas with a poor clinical outcome exist. The underlying genetic mechanisms and the genes involved remain obscure, even though chromosome 7p gains seem to be associated with these uncommon tumours. In this study, we compared two subsets of oestrogen receptor‐positive breast cancers, which differed in tumour grade, cytogenetic instability, and tumour proliferation, for their differential gene expression in order to identify proteins involved in the progression of oestrogen receptor‐positive breast cancers. We were able to show by means of subtractive suppression hybridization, real‐time reverse transcriptase PCR, and tissue microarray analysis that expression of the bone morphogenetic protein receptor IB (BMPR‐IB) is a major hallmark of the progression and dedifferentiation of breast cancer. Strong expression of BMPR‐IB was associated with high tumour grade, high tumour proliferation, cytogenetic instability, and a poor prognosis in oestrogen receptor‐positive carcinomas. Western blot analysis revealed that downstream signalling of this receptor is mainly mediated via phosphorylation of SMAD 1 in oestrogen receptor‐positive breast cancer. Even though BMPR‐IB was expressed in oestrogen receptor‐positive and ‐negative breast cancers, an impact on tumour grade, proliferation, and cytogenetic instability, as parameters of tumour progression, could only be demonstrated in oestrogen receptor‐positive carcinomas. This pro‐proliferative effect was complemented by significant anti‐apoptotic activity, indicated by XIAP and IAP‐2 expression in BMPR‐IB‐positive carcinomas. These results show that the BMP/SMAD pathway is activated in breast cancer and may contribute to breast cancer progression and dedifferentiation in oestrogen receptor‐positive breast cancer. The definition of this pathway characterizes a new potential target in the molecular treatment of invasive breast cancer. Copyright © 2005 Pathological Society of Great Britain and Ireland. Published by John Wiley &amp; Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley &amp; Sons, Ltd</pub><pmid>15892165</pmid><doi>10.1002/path.1785</doi><tpages>11</tpages></addata></record>
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subjects Apoptosis - genetics
Biological and medical sciences
Blotting, Western - methods
BMPR-IB
Bone Morphogenetic Protein Receptors, Type I
breast cancer
Breast Neoplasms - genetics
Breast Neoplasms - metabolism
Breast Neoplasms - pathology
Cell Differentiation - genetics
CGH
CXCR4
dedifferentiation
Disease Progression
DNA-Binding Proteins - genetics
DNA-Binding Proteins - metabolism
Female
Gene Expression Regulation, Neoplastic - genetics
Humans
Investigative techniques, diagnostic techniques (general aspects)
Medical sciences
Neoplasm Invasiveness
Neoplasm Proteins - genetics
Neoplasm Proteins - metabolism
Nucleic Acid Hybridization - methods
Oligonucleotide Array Sequence Analysis - methods
Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques
Peptides - analysis
progression
Protein-Serine-Threonine Kinases - metabolism
Receptors, CXCR4 - genetics
Receptors, Estrogen - genetics
Receptors, Estrogen - metabolism
Receptors, Growth Factor - metabolism
Reverse Transcriptase Polymerase Chain Reaction - methods
Signal Transduction - genetics
Smad Proteins
Smad1 Protein
Survival Analysis
Trans-Activators - genetics
Trans-Activators - metabolism
title First evidence supporting a potential role for the BMP/SMAD pathway in the progression of oestrogen receptor-positive breast cancer
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