Bone morphogenetic protein-2/4 and bone morphogenetic protein receptor type IA expression in metastatic and nonmetastatic oral squamous cell carcinoma

Abstract Purpose The study aimed to analyze the expression of bone morphogenetic protein-2/4 (BMP-2/4) and its receptor BMPR-IA (BMP receptor type IA) in metastatic and nonmetastatic oral squamous cell carcinoma (OSCC) and its implications for disease prognosis. Materials and methods The experimenta...

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Veröffentlicht in:American journal of otolaryngology 2010-07, Vol.31 (4), p.266-271
Hauptverfasser: Soares, Andréa Ferreira, DDs, MSc, PhD, Xavier, Ruth Lopes de Freitas, DDs, MSc, da Costa Miguel, Márcia Cristina, DDs, MSc, PhD, de Souza, Lélia Batista, DDs, MSc, PhD, Pinto, Leão Pereira, DDs, MSc, PhD
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container_issue 4
container_start_page 266
container_title American journal of otolaryngology
container_volume 31
creator Soares, Andréa Ferreira, DDs, MSc, PhD
Xavier, Ruth Lopes de Freitas, DDs, MSc
da Costa Miguel, Márcia Cristina, DDs, MSc, PhD
de Souza, Lélia Batista, DDs, MSc, PhD
Pinto, Leão Pereira, DDs, MSc, PhD
description Abstract Purpose The study aimed to analyze the expression of bone morphogenetic protein-2/4 (BMP-2/4) and its receptor BMPR-IA (BMP receptor type IA) in metastatic and nonmetastatic oral squamous cell carcinoma (OSCC) and its implications for disease prognosis. Materials and methods The experimental group included 16 cases of OSCC without metastasis and 7 cases of OSCC with metastasis. The presence or absence of nodal metastasis was used as a parameter for the evaluation of disease prognosis. Ten cases of oral fibroepithelial hyperplasia were selected as the control group. The expression of BMP-2/4 and BMPR-IA was analyzed by immunohistochemistry. Results In the experimental group with metastasis, strong expression of BMP-2/4 was observed in most cases (71.4%), whereas BMPR-IA exhibited weak expression (85.7%). In the experimental group without metastasis, there was strong expression of BMP-2/4 (62.5%) and BMPR-IA (100%). A significant association was observed between the prognosis of OSCC and the intensity of BMP-2/4 staining ( P = .002). Weak immunoreactivity to BMP-2/4 and BMPR-IA was observed in all control specimens. Conclusions The results suggest that strong expression of BMP-2/4, associated with low expression of BMPR-IA, observed in metastatic OSCC has a prognostic value, with the loss of responsiveness to BMPs through the loss of expression of their receptors being indicative of the development of metastasis.
doi_str_mv 10.1016/j.amjoto.2009.03.002
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Materials and methods The experimental group included 16 cases of OSCC without metastasis and 7 cases of OSCC with metastasis. The presence or absence of nodal metastasis was used as a parameter for the evaluation of disease prognosis. Ten cases of oral fibroepithelial hyperplasia were selected as the control group. The expression of BMP-2/4 and BMPR-IA was analyzed by immunohistochemistry. Results In the experimental group with metastasis, strong expression of BMP-2/4 was observed in most cases (71.4%), whereas BMPR-IA exhibited weak expression (85.7%). In the experimental group without metastasis, there was strong expression of BMP-2/4 (62.5%) and BMPR-IA (100%). A significant association was observed between the prognosis of OSCC and the intensity of BMP-2/4 staining ( P = .002). Weak immunoreactivity to BMP-2/4 and BMPR-IA was observed in all control specimens. Conclusions The results suggest that strong expression of BMP-2/4, associated with low expression of BMPR-IA, observed in metastatic OSCC has a prognostic value, with the loss of responsiveness to BMPs through the loss of expression of their receptors being indicative of the development of metastasis.</description><identifier>ISSN: 0196-0709</identifier><identifier>EISSN: 1532-818X</identifier><identifier>DOI: 10.1016/j.amjoto.2009.03.002</identifier><identifier>PMID: 20015767</identifier><identifier>CODEN: AJOTDP</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Biological and medical sciences ; Biomarkers, Tumor - biosynthesis ; Bone Morphogenetic Protein 4 - biosynthesis ; Bone Morphogenetic Protein Receptors, Type I - biosynthesis ; Cancer ; Carcinoma, Squamous Cell - metabolism ; Carcinoma, Squamous Cell - secondary ; Disease Progression ; Humans ; Immunohistochemistry ; Medical sciences ; Mouth Neoplasms - metabolism ; Mouth Neoplasms - pathology ; Neoplasm Metastasis ; Otolaryngology ; Otorhinolaryngology. 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Materials and methods The experimental group included 16 cases of OSCC without metastasis and 7 cases of OSCC with metastasis. The presence or absence of nodal metastasis was used as a parameter for the evaluation of disease prognosis. Ten cases of oral fibroepithelial hyperplasia were selected as the control group. The expression of BMP-2/4 and BMPR-IA was analyzed by immunohistochemistry. Results In the experimental group with metastasis, strong expression of BMP-2/4 was observed in most cases (71.4%), whereas BMPR-IA exhibited weak expression (85.7%). In the experimental group without metastasis, there was strong expression of BMP-2/4 (62.5%) and BMPR-IA (100%). A significant association was observed between the prognosis of OSCC and the intensity of BMP-2/4 staining ( P = .002). Weak immunoreactivity to BMP-2/4 and BMPR-IA was observed in all control specimens. 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Stomatology</subject><subject>Pathology</subject><subject>Prognosis</subject><subject>Proteins</subject><subject>Retrospective Studies</subject><subject>Studies</subject><subject>Surgery</subject><subject>Tumors</subject><subject>Upper respiratory tract, upper alimentary tract, paranasal sinuses, salivary glands: diseases, semeiology</subject><issn>0196-0709</issn><issn>1532-818X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkt-K1DAUxoMo7rj6BiIBEa_aPUnaTnoj7C7-WVjwQgXvQiY91dQ26SapOC_i85oyoysLIrkIJL_v5Dv5DiFPGZQMWHM2lHoafPIlB2hLECUAv0c2rBa8kEx-vk82wNqmgC20J-RRjAMAiErUD8lJlrB622w35OeFd0gnH-av_gs6TNbQOfiE1hX8rKLadXT3T4QGNDgnH2jaz0ivzin-mAPGaL2j-XrCpGPSq2It5Lz768QHPdJ4s-jJL5EaHEdqdDDW-Uk_Jg96PUZ8ctxPyac3rz9eviuu37-9ujy_LkzNIRVNr7eyb7FnjGmEjne1qbEGkPlEVlj3rIemEpIZ3muUhrFe6gZauUMpKiNOyctD3dzQzYIxqcnG1Yp2mF2prRCtBM6qTD6_Qw5-CS6bUwwEE41oOWSqOlAm-BgD9moOdtJhnyG1xqYGdYhNrbEpECrHlmXPjsWX3YTdH9HvnDLw4gjoaPTYB-2MjbecyFEDbzL36sBh_rTvFoOKxqIz2NkcVVKdt_9zcreAGa2z-c1vuMd427OKXIH6sI7YOmF5AeRMxC-YKM8H</recordid><startdate>20100701</startdate><enddate>20100701</enddate><creator>Soares, Andréa Ferreira, DDs, MSc, PhD</creator><creator>Xavier, Ruth Lopes de Freitas, DDs, MSc</creator><creator>da Costa Miguel, Márcia Cristina, DDs, MSc, PhD</creator><creator>de Souza, Lélia Batista, DDs, MSc, PhD</creator><creator>Pinto, Leão Pereira, DDs, MSc, PhD</creator><general>Elsevier Inc</general><general>Elsevier</general><general>Elsevier Limited</general><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>7QO</scope><scope>7QR</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20100701</creationdate><title>Bone morphogenetic protein-2/4 and bone morphogenetic protein receptor type IA expression in metastatic and nonmetastatic oral squamous cell carcinoma</title><author>Soares, Andréa Ferreira, DDs, MSc, PhD ; Xavier, Ruth Lopes de Freitas, DDs, MSc ; da Costa Miguel, Márcia Cristina, DDs, MSc, PhD ; de Souza, Lélia Batista, DDs, MSc, PhD ; Pinto, Leão Pereira, DDs, MSc, PhD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c520t-6fa78f9ef111ae0d2d5c5e5008f1184e5f1f064381c2fae8c11f8a6098be834c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Biological and medical sciences</topic><topic>Biomarkers, Tumor - biosynthesis</topic><topic>Bone Morphogenetic Protein 4 - biosynthesis</topic><topic>Bone Morphogenetic Protein Receptors, Type I - biosynthesis</topic><topic>Cancer</topic><topic>Carcinoma, Squamous Cell - metabolism</topic><topic>Carcinoma, Squamous Cell - secondary</topic><topic>Disease Progression</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Medical sciences</topic><topic>Mouth Neoplasms - metabolism</topic><topic>Mouth Neoplasms - pathology</topic><topic>Neoplasm Metastasis</topic><topic>Otolaryngology</topic><topic>Otorhinolaryngology. Stomatology</topic><topic>Pathology</topic><topic>Prognosis</topic><topic>Proteins</topic><topic>Retrospective Studies</topic><topic>Studies</topic><topic>Surgery</topic><topic>Tumors</topic><topic>Upper respiratory tract, upper alimentary tract, paranasal sinuses, salivary glands: diseases, semeiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Soares, Andréa Ferreira, DDs, MSc, PhD</creatorcontrib><creatorcontrib>Xavier, Ruth Lopes de Freitas, DDs, MSc</creatorcontrib><creatorcontrib>da Costa Miguel, Márcia Cristina, DDs, MSc, PhD</creatorcontrib><creatorcontrib>de Souza, Lélia Batista, DDs, MSc, PhD</creatorcontrib><creatorcontrib>Pinto, Leão Pereira, DDs, MSc, PhD</creatorcontrib><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>Biotechnology Research Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of otolaryngology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Soares, Andréa Ferreira, DDs, MSc, PhD</au><au>Xavier, Ruth Lopes de Freitas, DDs, MSc</au><au>da Costa Miguel, Márcia Cristina, DDs, MSc, PhD</au><au>de Souza, Lélia Batista, DDs, MSc, PhD</au><au>Pinto, Leão Pereira, DDs, MSc, PhD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bone morphogenetic protein-2/4 and bone morphogenetic protein receptor type IA expression in metastatic and nonmetastatic oral squamous cell carcinoma</atitle><jtitle>American journal of otolaryngology</jtitle><addtitle>Am J Otolaryngol</addtitle><date>2010-07-01</date><risdate>2010</risdate><volume>31</volume><issue>4</issue><spage>266</spage><epage>271</epage><pages>266-271</pages><issn>0196-0709</issn><eissn>1532-818X</eissn><coden>AJOTDP</coden><abstract>Abstract Purpose The study aimed to analyze the expression of bone morphogenetic protein-2/4 (BMP-2/4) and its receptor BMPR-IA (BMP receptor type IA) in metastatic and nonmetastatic oral squamous cell carcinoma (OSCC) and its implications for disease prognosis. Materials and methods The experimental group included 16 cases of OSCC without metastasis and 7 cases of OSCC with metastasis. The presence or absence of nodal metastasis was used as a parameter for the evaluation of disease prognosis. Ten cases of oral fibroepithelial hyperplasia were selected as the control group. The expression of BMP-2/4 and BMPR-IA was analyzed by immunohistochemistry. Results In the experimental group with metastasis, strong expression of BMP-2/4 was observed in most cases (71.4%), whereas BMPR-IA exhibited weak expression (85.7%). In the experimental group without metastasis, there was strong expression of BMP-2/4 (62.5%) and BMPR-IA (100%). A significant association was observed between the prognosis of OSCC and the intensity of BMP-2/4 staining ( P = .002). Weak immunoreactivity to BMP-2/4 and BMPR-IA was observed in all control specimens. Conclusions The results suggest that strong expression of BMP-2/4, associated with low expression of BMPR-IA, observed in metastatic OSCC has a prognostic value, with the loss of responsiveness to BMPs through the loss of expression of their receptors being indicative of the development of metastasis.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>20015767</pmid><doi>10.1016/j.amjoto.2009.03.002</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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subjects Biological and medical sciences
Biomarkers, Tumor - biosynthesis
Bone Morphogenetic Protein 4 - biosynthesis
Bone Morphogenetic Protein Receptors, Type I - biosynthesis
Cancer
Carcinoma, Squamous Cell - metabolism
Carcinoma, Squamous Cell - secondary
Disease Progression
Humans
Immunohistochemistry
Medical sciences
Mouth Neoplasms - metabolism
Mouth Neoplasms - pathology
Neoplasm Metastasis
Otolaryngology
Otorhinolaryngology. Stomatology
Pathology
Prognosis
Proteins
Retrospective Studies
Studies
Surgery
Tumors
Upper respiratory tract, upper alimentary tract, paranasal sinuses, salivary glands: diseases, semeiology
title Bone morphogenetic protein-2/4 and bone morphogenetic protein receptor type IA expression in metastatic and nonmetastatic oral squamous cell carcinoma
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