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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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 & 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 & 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. 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</subject><ispartof>The Journal of pathology, 2005-07, Vol.206 (3), p.366-376</ispartof><rights>Copyright © 2005 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.</rights><rights>2005 INIST-CNRS</rights><rights>Copyright 2005 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4225-f6e034b16e35f3e789a6aadde265189387ad7cda46c5fa816c86830507af62813</citedby><cites>FETCH-LOGICAL-c4225-f6e034b16e35f3e789a6aadde265189387ad7cda46c5fa816c86830507af62813</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fpath.1785$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fpath.1785$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16877339$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15892165$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Helms, Mike W</creatorcontrib><creatorcontrib>Packeisen, Jens</creatorcontrib><creatorcontrib>August, Christian</creatorcontrib><creatorcontrib>Schittek, Birgit</creatorcontrib><creatorcontrib>Boecker, Werner</creatorcontrib><creatorcontrib>Brandt, Burkhard H</creatorcontrib><creatorcontrib>Buerger, Horst</creatorcontrib><title>First evidence supporting a potential role for the BMP/SMAD pathway in the progression of oestrogen receptor-positive breast cancer</title><title>The Journal of pathology</title><addtitle>J. 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. Published by John Wiley & Sons, Ltd.</description><subject>Apoptosis - genetics</subject><subject>Biological and medical sciences</subject><subject>Blotting, Western - methods</subject><subject>BMPR-IB</subject><subject>Bone Morphogenetic Protein Receptors, Type I</subject><subject>breast cancer</subject><subject>Breast Neoplasms - genetics</subject><subject>Breast Neoplasms - metabolism</subject><subject>Breast Neoplasms - pathology</subject><subject>Cell Differentiation - genetics</subject><subject>CGH</subject><subject>CXCR4</subject><subject>dedifferentiation</subject><subject>Disease Progression</subject><subject>DNA-Binding Proteins - genetics</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>Female</subject><subject>Gene Expression Regulation, Neoplastic - genetics</subject><subject>Humans</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Medical sciences</subject><subject>Neoplasm Invasiveness</subject><subject>Neoplasm Proteins - genetics</subject><subject>Neoplasm Proteins - metabolism</subject><subject>Nucleic Acid Hybridization - methods</subject><subject>Oligonucleotide Array Sequence Analysis - methods</subject><subject>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</subject><subject>Peptides - analysis</subject><subject>progression</subject><subject>Protein-Serine-Threonine Kinases - metabolism</subject><subject>Receptors, CXCR4 - genetics</subject><subject>Receptors, Estrogen - genetics</subject><subject>Receptors, Estrogen - metabolism</subject><subject>Receptors, Growth Factor - metabolism</subject><subject>Reverse Transcriptase Polymerase Chain Reaction - methods</subject><subject>Signal Transduction - genetics</subject><subject>Smad Proteins</subject><subject>Smad1 Protein</subject><subject>Survival Analysis</subject><subject>Trans-Activators - genetics</subject><subject>Trans-Activators - metabolism</subject><issn>0022-3417</issn><issn>1096-9896</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtvEzEQgC0EoqFw4A8gX0DisI29jl_HpJAG1IZKLeJoOd7Z1rBZb-1NS878cbxkRU-Ik6XxN_PNA6HXlJxQQsppZ_vbEyoVf4ImlGhRaKXFUzTJf2XBZlQeoRcpfSeEaM35c3REudIlFXyCfi19TD2Ge19B6wCnXdeF2Pv2BlvchR7a3tsGx9AArkPE_S3gxcXl9Opi_gEP3ge7x779E-9iuImQkg8tDjUOkPocgRZHcND1IRZdSL7394A3EWzWOpud8SV6VtsmwavxPUZflx-vT1fF-ZezT6fz88LNypIXtQDCZhsqgPGagVTaCmurCkrBqdJMSVtJV9mZcLy2igqnhGKEE2lrUSrKjtG7Q93c6N0ud2e2PjloGttC2CUjpKa6ZP8HqWRMzegAvj-ALoaUItSmi35r495QYobTmGFFZjhNZt-MRXebLVSP5HiLDLwdAZucbeqYl-PTIyeUzF6duemBe_AN7P9tNJfz69WoLg4ZPvXw82-GjT_yzExy8219ZpaLdbn-vLoyC_Yb7862fw</recordid><startdate>200507</startdate><enddate>200507</enddate><creator>Helms, Mike W</creator><creator>Packeisen, Jens</creator><creator>August, Christian</creator><creator>Schittek, Birgit</creator><creator>Boecker, Werner</creator><creator>Brandt, Burkhard H</creator><creator>Buerger, Horst</creator><general>John Wiley & Sons, Ltd</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TO</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>200507</creationdate><title>First evidence supporting a potential role for the BMP/SMAD pathway in the progression of oestrogen receptor-positive breast cancer</title><author>Helms, Mike W ; Packeisen, Jens ; August, Christian ; Schittek, Birgit ; Boecker, Werner ; Brandt, Burkhard H ; Buerger, Horst</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4225-f6e034b16e35f3e789a6aadde265189387ad7cda46c5fa816c86830507af62813</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Apoptosis - genetics</topic><topic>Biological and medical sciences</topic><topic>Blotting, Western - methods</topic><topic>BMPR-IB</topic><topic>Bone Morphogenetic Protein Receptors, Type I</topic><topic>breast cancer</topic><topic>Breast Neoplasms - genetics</topic><topic>Breast Neoplasms - metabolism</topic><topic>Breast Neoplasms - pathology</topic><topic>Cell Differentiation - genetics</topic><topic>CGH</topic><topic>CXCR4</topic><topic>dedifferentiation</topic><topic>Disease Progression</topic><topic>DNA-Binding Proteins - genetics</topic><topic>DNA-Binding Proteins - metabolism</topic><topic>Female</topic><topic>Gene Expression Regulation, Neoplastic - genetics</topic><topic>Humans</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Medical sciences</topic><topic>Neoplasm Invasiveness</topic><topic>Neoplasm Proteins - genetics</topic><topic>Neoplasm Proteins - metabolism</topic><topic>Nucleic Acid Hybridization - methods</topic><topic>Oligonucleotide Array Sequence Analysis - methods</topic><topic>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</topic><topic>Peptides - analysis</topic><topic>progression</topic><topic>Protein-Serine-Threonine Kinases - metabolism</topic><topic>Receptors, CXCR4 - genetics</topic><topic>Receptors, Estrogen - genetics</topic><topic>Receptors, Estrogen - metabolism</topic><topic>Receptors, Growth Factor - metabolism</topic><topic>Reverse Transcriptase Polymerase Chain Reaction - methods</topic><topic>Signal Transduction - genetics</topic><topic>Smad Proteins</topic><topic>Smad1 Protein</topic><topic>Survival Analysis</topic><topic>Trans-Activators - genetics</topic><topic>Trans-Activators - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Helms, Mike W</creatorcontrib><creatorcontrib>Packeisen, Jens</creatorcontrib><creatorcontrib>August, Christian</creatorcontrib><creatorcontrib>Schittek, Birgit</creatorcontrib><creatorcontrib>Boecker, Werner</creatorcontrib><creatorcontrib>Brandt, Burkhard H</creatorcontrib><creatorcontrib>Buerger, Horst</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Helms, Mike W</au><au>Packeisen, Jens</au><au>August, Christian</au><au>Schittek, Birgit</au><au>Boecker, Werner</au><au>Brandt, Burkhard H</au><au>Buerger, Horst</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>First evidence supporting a potential role for the BMP/SMAD pathway in the progression of oestrogen receptor-positive breast cancer</atitle><jtitle>The Journal of pathology</jtitle><addtitle>J. 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 & Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley & 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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