Expression of LDL receptor‐related protein 5 (LRP5) as a novel marker for disease progression in high‐grade osteosarcoma
The Wingless‐type (Wnt) family of proteins and its coreceptor LRP5 have recently been implicated in human skeletal development. Wnt pathway modulates cell fate and cell proliferation during embryonic development and carcinogenesis through activation of receptor‐mediated signaling. Osteosarcoma (OS)...
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Veröffentlicht in: | International journal of cancer 2004-03, Vol.109 (1), p.106-111 |
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container_title | International journal of cancer |
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creator | Hoang, Bang H. Kubo, Tadahiko Healey, John H. Sowers, Rebecca Mazza, BethAnne Yang, Rui Huvos, Andrew G. Meyers, Paul A. Gorlick, Richard |
description | The Wingless‐type (Wnt) family of proteins and its coreceptor LRP5 have recently been implicated in human skeletal development. Wnt pathway modulates cell fate and cell proliferation during embryonic development and carcinogenesis through activation of receptor‐mediated signaling. Osteosarcoma (OS) is a bone‐forming tumor of mesenchymal origin whose growth control has been linked to autocrine or paracrine stimulation by several growth factor families. We examined 4 OS cell lines for WNT1, WNT4, WNT5A, WNT7A, WNT11, FZD1‐10 and LRP5 expression by reverse transcription polymerase chain reaction (RT‐PCR). In addition, RT‐PCR for LRP5 expression was performed in 44 OS patient samples and the findings were correlated with clinical data. Expression profiling of Wnts and their receptors revealed the presence of several isoforms in OS cell lines. Overall, 22/44 (50%) of OS patient samples showed evidence of LRP5 expression. Presence of LRP5 correlated significantly with tumor metastasis (p = 0.005) and the chondroblastic subtype of OS (p = 0.045). In addition, patients whose tumors were positive for LRP5 showed a trend toward decreased event‐free survival (p = 0.066). No significant association was found between LRP5 expression and age, gender, site of disease, site of metastasis or degree of chemotherapy‐induced tumor necrosis. Sequencing of exon 3 of LRP5 in 10 OS patient‐derived cell cultures showed no activating mutation of LRP5. These results showed that expression of LRP5 is a common event in OS and strongly suggest a role for LRP and Wnt signaling in the pathobiology and progression of this disease. © 2003 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/ijc.11677 |
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Wnt pathway modulates cell fate and cell proliferation during embryonic development and carcinogenesis through activation of receptor‐mediated signaling. Osteosarcoma (OS) is a bone‐forming tumor of mesenchymal origin whose growth control has been linked to autocrine or paracrine stimulation by several growth factor families. We examined 4 OS cell lines for WNT1, WNT4, WNT5A, WNT7A, WNT11, FZD1‐10 and LRP5 expression by reverse transcription polymerase chain reaction (RT‐PCR). In addition, RT‐PCR for LRP5 expression was performed in 44 OS patient samples and the findings were correlated with clinical data. Expression profiling of Wnts and their receptors revealed the presence of several isoforms in OS cell lines. Overall, 22/44 (50%) of OS patient samples showed evidence of LRP5 expression. Presence of LRP5 correlated significantly with tumor metastasis (p = 0.005) and the chondroblastic subtype of OS (p = 0.045). In addition, patients whose tumors were positive for LRP5 showed a trend toward decreased event‐free survival (p = 0.066). No significant association was found between LRP5 expression and age, gender, site of disease, site of metastasis or degree of chemotherapy‐induced tumor necrosis. Sequencing of exon 3 of LRP5 in 10 OS patient‐derived cell cultures showed no activating mutation of LRP5. These results showed that expression of LRP5 is a common event in OS and strongly suggest a role for LRP and Wnt signaling in the pathobiology and progression of this disease. © 2003 Wiley‐Liss, Inc.</description><identifier>ISSN: 0020-7136</identifier><identifier>EISSN: 1097-0215</identifier><identifier>DOI: 10.1002/ijc.11677</identifier><identifier>PMID: 14735475</identifier><identifier>CODEN: IJCNAW</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adolescent ; Adult ; Aged ; beta Catenin ; Biological and medical sciences ; Cell Division ; Cell Line, Tumor ; Cell Lineage ; Child ; Child, Preschool ; Chondrocytes - metabolism ; Cytoskeletal Proteins - metabolism ; Disease Progression ; Diseases of the osteoarticular system ; Exons ; Female ; Genetic Markers ; Humans ; Immunohistochemistry ; Infant ; LDL-Receptor Related Proteins ; Low Density Lipoprotein Receptor-Related Protein-5 ; low‐density lipoprotein receptor‐related protein ; Male ; Medical sciences ; metastasis ; Middle Aged ; Mutation ; Neoplasm Metastasis ; osteosarcoma ; Osteosarcoma - metabolism ; Osteosarcoma - pathology ; Protein Isoforms ; Receptors, LDL - biosynthesis ; Reverse Transcriptase Polymerase Chain Reaction ; Sequence Analysis, DNA ; Signal Transduction ; survival ; Time Factors ; Trans-Activators - metabolism ; Treatment Outcome ; Tumors of striated muscle and skeleton ; Wnt</subject><ispartof>International journal of cancer, 2004-03, Vol.109 (1), p.106-111</ispartof><rights>Copyright © 2003 Wiley‐Liss, Inc.</rights><rights>2004 INIST-CNRS</rights><rights>Copyright 2003 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4487-5c0be86d3e9dbd8d449af67609b68c6825134656f7806ca0f4b2f01d3b506a9e3</citedby><cites>FETCH-LOGICAL-c4487-5c0be86d3e9dbd8d449af67609b68c6825134656f7806ca0f4b2f01d3b506a9e3</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%2Fijc.11677$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fijc.11677$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15444780$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14735475$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hoang, Bang H.</creatorcontrib><creatorcontrib>Kubo, Tadahiko</creatorcontrib><creatorcontrib>Healey, John H.</creatorcontrib><creatorcontrib>Sowers, Rebecca</creatorcontrib><creatorcontrib>Mazza, BethAnne</creatorcontrib><creatorcontrib>Yang, Rui</creatorcontrib><creatorcontrib>Huvos, Andrew G.</creatorcontrib><creatorcontrib>Meyers, Paul A.</creatorcontrib><creatorcontrib>Gorlick, Richard</creatorcontrib><title>Expression of LDL receptor‐related protein 5 (LRP5) as a novel marker for disease progression in high‐grade osteosarcoma</title><title>International journal of cancer</title><addtitle>Int J Cancer</addtitle><description>The Wingless‐type (Wnt) family of proteins and its coreceptor LRP5 have recently been implicated in human skeletal development. Wnt pathway modulates cell fate and cell proliferation during embryonic development and carcinogenesis through activation of receptor‐mediated signaling. Osteosarcoma (OS) is a bone‐forming tumor of mesenchymal origin whose growth control has been linked to autocrine or paracrine stimulation by several growth factor families. We examined 4 OS cell lines for WNT1, WNT4, WNT5A, WNT7A, WNT11, FZD1‐10 and LRP5 expression by reverse transcription polymerase chain reaction (RT‐PCR). In addition, RT‐PCR for LRP5 expression was performed in 44 OS patient samples and the findings were correlated with clinical data. Expression profiling of Wnts and their receptors revealed the presence of several isoforms in OS cell lines. Overall, 22/44 (50%) of OS patient samples showed evidence of LRP5 expression. Presence of LRP5 correlated significantly with tumor metastasis (p = 0.005) and the chondroblastic subtype of OS (p = 0.045). In addition, patients whose tumors were positive for LRP5 showed a trend toward decreased event‐free survival (p = 0.066). No significant association was found between LRP5 expression and age, gender, site of disease, site of metastasis or degree of chemotherapy‐induced tumor necrosis. Sequencing of exon 3 of LRP5 in 10 OS patient‐derived cell cultures showed no activating mutation of LRP5. These results showed that expression of LRP5 is a common event in OS and strongly suggest a role for LRP and Wnt signaling in the pathobiology and progression of this disease. © 2003 Wiley‐Liss, Inc.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>beta Catenin</subject><subject>Biological and medical sciences</subject><subject>Cell Division</subject><subject>Cell Line, Tumor</subject><subject>Cell Lineage</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Chondrocytes - metabolism</subject><subject>Cytoskeletal Proteins - metabolism</subject><subject>Disease Progression</subject><subject>Diseases of the osteoarticular system</subject><subject>Exons</subject><subject>Female</subject><subject>Genetic Markers</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Infant</subject><subject>LDL-Receptor Related Proteins</subject><subject>Low Density Lipoprotein Receptor-Related Protein-5</subject><subject>low‐density lipoprotein receptor‐related protein</subject><subject>Male</subject><subject>Medical sciences</subject><subject>metastasis</subject><subject>Middle Aged</subject><subject>Mutation</subject><subject>Neoplasm Metastasis</subject><subject>osteosarcoma</subject><subject>Osteosarcoma - metabolism</subject><subject>Osteosarcoma - pathology</subject><subject>Protein Isoforms</subject><subject>Receptors, LDL - biosynthesis</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Sequence Analysis, DNA</subject><subject>Signal Transduction</subject><subject>survival</subject><subject>Time Factors</subject><subject>Trans-Activators - metabolism</subject><subject>Treatment Outcome</subject><subject>Tumors of striated muscle and skeleton</subject><subject>Wnt</subject><issn>0020-7136</issn><issn>1097-0215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10M9OFTEUBvDGaOQKLHwB040EFgPtTP_MLM0VFTMJhMh60mlPL8W502vPXITEhY_gM_IkFO81rFx10V-_c_oR8pazY85YeRJu7DHnSusXZMZZowtWcvmSzPIdKzSv1A55g3jDGOeSiddkhwtdSaHljPw6vVslQAxxpNHT9mNLE1hYTTE9_P6TYDATOLpKcYIwUkkP28sLeUQNUkPHeAsDXZr0HRL1MVEXEAzCE1_8C82vrsPiOoctknFAI04Q0SQbl2aPvPJmQNjfnrvk6tPpt_mXoj3_fDb_0BZWiFoX0rIeauUqaFzvaidEY7zSijW9qq2qS8kroaTyumbKGuZFX3rGXdVLpkwD1S452OTmxX6sAaduGdDCMJgR4ho73pRV1XCV4dEG2hQRE_hulUL-4H3HWfdUdZer7v5Wne27bei6X4J7lttuM3i_BQatGXwyow347KQQIm-c3cnG_QwD3P9_Ynf2db4Z_QgP05cK</recordid><startdate>20040310</startdate><enddate>20040310</enddate><creator>Hoang, Bang H.</creator><creator>Kubo, Tadahiko</creator><creator>Healey, John H.</creator><creator>Sowers, Rebecca</creator><creator>Mazza, BethAnne</creator><creator>Yang, Rui</creator><creator>Huvos, Andrew G.</creator><creator>Meyers, Paul A.</creator><creator>Gorlick, Richard</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</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>7TO</scope><scope>H94</scope></search><sort><creationdate>20040310</creationdate><title>Expression of LDL receptor‐related protein 5 (LRP5) as a novel marker for disease progression in high‐grade osteosarcoma</title><author>Hoang, Bang H. ; Kubo, Tadahiko ; Healey, John H. ; Sowers, Rebecca ; Mazza, BethAnne ; Yang, Rui ; Huvos, Andrew G. ; Meyers, Paul A. ; Gorlick, Richard</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4487-5c0be86d3e9dbd8d449af67609b68c6825134656f7806ca0f4b2f01d3b506a9e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>beta Catenin</topic><topic>Biological and medical sciences</topic><topic>Cell Division</topic><topic>Cell Line, Tumor</topic><topic>Cell Lineage</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Chondrocytes - metabolism</topic><topic>Cytoskeletal Proteins - metabolism</topic><topic>Disease Progression</topic><topic>Diseases of the osteoarticular system</topic><topic>Exons</topic><topic>Female</topic><topic>Genetic Markers</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Infant</topic><topic>LDL-Receptor Related Proteins</topic><topic>Low Density Lipoprotein Receptor-Related Protein-5</topic><topic>low‐density lipoprotein receptor‐related protein</topic><topic>Male</topic><topic>Medical sciences</topic><topic>metastasis</topic><topic>Middle Aged</topic><topic>Mutation</topic><topic>Neoplasm Metastasis</topic><topic>osteosarcoma</topic><topic>Osteosarcoma - metabolism</topic><topic>Osteosarcoma - pathology</topic><topic>Protein Isoforms</topic><topic>Receptors, LDL - biosynthesis</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>Sequence Analysis, DNA</topic><topic>Signal Transduction</topic><topic>survival</topic><topic>Time Factors</topic><topic>Trans-Activators - metabolism</topic><topic>Treatment Outcome</topic><topic>Tumors of striated muscle and skeleton</topic><topic>Wnt</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hoang, Bang H.</creatorcontrib><creatorcontrib>Kubo, Tadahiko</creatorcontrib><creatorcontrib>Healey, John H.</creatorcontrib><creatorcontrib>Sowers, Rebecca</creatorcontrib><creatorcontrib>Mazza, BethAnne</creatorcontrib><creatorcontrib>Yang, Rui</creatorcontrib><creatorcontrib>Huvos, Andrew G.</creatorcontrib><creatorcontrib>Meyers, Paul A.</creatorcontrib><creatorcontrib>Gorlick, Richard</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>Oncogenes and Growth Factors Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>International journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hoang, Bang H.</au><au>Kubo, Tadahiko</au><au>Healey, John H.</au><au>Sowers, Rebecca</au><au>Mazza, BethAnne</au><au>Yang, Rui</au><au>Huvos, Andrew G.</au><au>Meyers, Paul A.</au><au>Gorlick, Richard</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression of LDL receptor‐related protein 5 (LRP5) as a novel marker for disease progression in high‐grade osteosarcoma</atitle><jtitle>International journal of cancer</jtitle><addtitle>Int J Cancer</addtitle><date>2004-03-10</date><risdate>2004</risdate><volume>109</volume><issue>1</issue><spage>106</spage><epage>111</epage><pages>106-111</pages><issn>0020-7136</issn><eissn>1097-0215</eissn><coden>IJCNAW</coden><abstract>The Wingless‐type (Wnt) family of proteins and its coreceptor LRP5 have recently been implicated in human skeletal development. Wnt pathway modulates cell fate and cell proliferation during embryonic development and carcinogenesis through activation of receptor‐mediated signaling. Osteosarcoma (OS) is a bone‐forming tumor of mesenchymal origin whose growth control has been linked to autocrine or paracrine stimulation by several growth factor families. We examined 4 OS cell lines for WNT1, WNT4, WNT5A, WNT7A, WNT11, FZD1‐10 and LRP5 expression by reverse transcription polymerase chain reaction (RT‐PCR). In addition, RT‐PCR for LRP5 expression was performed in 44 OS patient samples and the findings were correlated with clinical data. Expression profiling of Wnts and their receptors revealed the presence of several isoforms in OS cell lines. Overall, 22/44 (50%) of OS patient samples showed evidence of LRP5 expression. Presence of LRP5 correlated significantly with tumor metastasis (p = 0.005) and the chondroblastic subtype of OS (p = 0.045). In addition, patients whose tumors were positive for LRP5 showed a trend toward decreased event‐free survival (p = 0.066). No significant association was found between LRP5 expression and age, gender, site of disease, site of metastasis or degree of chemotherapy‐induced tumor necrosis. Sequencing of exon 3 of LRP5 in 10 OS patient‐derived cell cultures showed no activating mutation of LRP5. These results showed that expression of LRP5 is a common event in OS and strongly suggest a role for LRP and Wnt signaling in the pathobiology and progression of this disease. © 2003 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>14735475</pmid><doi>10.1002/ijc.11677</doi><tpages>6</tpages></addata></record> |
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subjects | Adolescent Adult Aged beta Catenin Biological and medical sciences Cell Division Cell Line, Tumor Cell Lineage Child Child, Preschool Chondrocytes - metabolism Cytoskeletal Proteins - metabolism Disease Progression Diseases of the osteoarticular system Exons Female Genetic Markers Humans Immunohistochemistry Infant LDL-Receptor Related Proteins Low Density Lipoprotein Receptor-Related Protein-5 low‐density lipoprotein receptor‐related protein Male Medical sciences metastasis Middle Aged Mutation Neoplasm Metastasis osteosarcoma Osteosarcoma - metabolism Osteosarcoma - pathology Protein Isoforms Receptors, LDL - biosynthesis Reverse Transcriptase Polymerase Chain Reaction Sequence Analysis, DNA Signal Transduction survival Time Factors Trans-Activators - metabolism Treatment Outcome Tumors of striated muscle and skeleton Wnt |
title | Expression of LDL receptor‐related protein 5 (LRP5) as a novel marker for disease progression in high‐grade osteosarcoma |
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