Micro‐RNA profiles in osteosarcoma as a predictive tool for ifosfamide response
Micro‐RNAs (miRNA) are currently used as cancer biomarkers for hematological cancers and solid tumors. Osteosarcoma is the first primary malignant bone tumor, characterized by a complex genetic and resistance to conventional treatments. For this latter property, the median survival has not been impr...
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Veröffentlicht in: | International journal of cancer 2011-08, Vol.129 (3), p.680-690 |
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creator | Gougelet, Angélique Pissaloux, Daniel Besse, Anthony Perez, Jennifer Duc, Adeline Dutour, Aurélie Blay, Jean‐Yves Alberti, Laurent |
description | Micro‐RNAs (miRNA) are currently used as cancer biomarkers for hematological cancers and solid tumors. Osteosarcoma is the first primary malignant bone tumor, characterized by a complex genetic and resistance to conventional treatments. For this latter property, the median survival has not been improved since 1990 despite preoperative administration of chemotherapeutic agents. The prediction of tumor response before chemotherapy treatment would constitute a major progress for this pathology. We assessed in this study if miRNA profiling could surpass the current limitations for osteosarcoma diagnosis. We measured the miRNA expression in different osteosarcoma samples: (i) 27 osteosarcoma paraffin‐embedded tumors from patients, (ii) human osteosarcoma cell lines, and (iii) tumors from a syngeneic rat osteosarcoma model, recapitulating human osteosarcoma. miRNA profiles were determined using microfluidic cards performing high‐throughput TaqMan®‐based PCR assays, called TaqMan® Low Density Arrays. Osteosarcoma of rat and human origins showed a miRNA signature, which could discriminate good from bad responders. In particular, we identified five discriminating miRNAs (miR‐92a, miR‐99b, miR‐132, miR‐193a‐5p and miR‐422a) in patient tumors, which could be easily transferable to diagnosis. These discriminating miRNAs, as well as those identified in rat, targeted the TGFβ, the Wnt and the MAP kinase pathways. These results indicate that our platform constitutes a potent diagnostic tool to predict tumor sensitivity to a drug in attempt to better adapt treatment to tumor biological specificities and also to identify new potential therapeutic strategies. |
doi_str_mv | 10.1002/ijc.25715 |
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Osteosarcoma is the first primary malignant bone tumor, characterized by a complex genetic and resistance to conventional treatments. For this latter property, the median survival has not been improved since 1990 despite preoperative administration of chemotherapeutic agents. The prediction of tumor response before chemotherapy treatment would constitute a major progress for this pathology. We assessed in this study if miRNA profiling could surpass the current limitations for osteosarcoma diagnosis. We measured the miRNA expression in different osteosarcoma samples: (i) 27 osteosarcoma paraffin‐embedded tumors from patients, (ii) human osteosarcoma cell lines, and (iii) tumors from a syngeneic rat osteosarcoma model, recapitulating human osteosarcoma. miRNA profiles were determined using microfluidic cards performing high‐throughput TaqMan®‐based PCR assays, called TaqMan® Low Density Arrays. Osteosarcoma of rat and human origins showed a miRNA signature, which could discriminate good from bad responders. In particular, we identified five discriminating miRNAs (miR‐92a, miR‐99b, miR‐132, miR‐193a‐5p and miR‐422a) in patient tumors, which could be easily transferable to diagnosis. These discriminating miRNAs, as well as those identified in rat, targeted the TGFβ, the Wnt and the MAP kinase pathways. These results indicate that our platform constitutes a potent diagnostic tool to predict tumor sensitivity to a drug in attempt to better adapt treatment to tumor biological specificities and also to identify new potential therapeutic strategies.</description><identifier>ISSN: 0020-7136</identifier><identifier>ISSN: 1097-0215</identifier><identifier>EISSN: 1097-0215</identifier><identifier>DOI: 10.1002/ijc.25715</identifier><identifier>PMID: 20949564</identifier><identifier>CODEN: IJCNAW</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Animal models ; Animals ; Antineoplastic Agents - therapeutic use ; Biological and medical sciences ; biomarkers ; Bone Neoplasms - drug therapy ; Bone Neoplasms - genetics ; Bone tumors ; Cancer ; Cell Cycle ; Cell Line, Tumor ; Chemotherapy ; diagnosis ; Disease Models, Animal ; Diseases of the osteoarticular system ; Drugs ; Gene Expression Profiling ; Humans ; Ifosfamide ; Ifosfamide - therapeutic use ; Life Sciences ; MAP kinase ; Medical sciences ; Microfluidics ; MicroRNAs - genetics ; MicroRNAs - metabolism ; miRNA ; miRNA profiling ; Neoplasm Invasiveness ; Osteosarcoma ; Osteosarcoma - drug therapy ; Osteosarcoma - genetics ; Osteosarcoma cells ; Polymerase chain reaction ; Rats ; Solid tumors ; Survival ; targeted therapy ; Treatment Outcome ; Tumors ; Tumors of striated muscle and skeleton ; Wnt protein</subject><ispartof>International journal of cancer, 2011-08, Vol.129 (3), p.680-690</ispartof><rights>Copyright © 2010 UICC</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2010 UICC.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5255-73cf9564d5b788d5abd21a577b2eafb3c38614bf2060c2dd7b9d7e62fb0d1f753</citedby><cites>FETCH-LOGICAL-c5255-73cf9564d5b788d5abd21a577b2eafb3c38614bf2060c2dd7b9d7e62fb0d1f753</cites><orcidid>0000-0002-7686-1750 ; 0000-0001-5741-3576 ; 0000-0001-7190-120X</orcidid></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.25715$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fijc.25715$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,780,784,885,1416,27915,27916,45565,45566</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24281302$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20949564$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://inserm.hal.science/inserm-02532865$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Gougelet, Angélique</creatorcontrib><creatorcontrib>Pissaloux, Daniel</creatorcontrib><creatorcontrib>Besse, Anthony</creatorcontrib><creatorcontrib>Perez, Jennifer</creatorcontrib><creatorcontrib>Duc, Adeline</creatorcontrib><creatorcontrib>Dutour, Aurélie</creatorcontrib><creatorcontrib>Blay, Jean‐Yves</creatorcontrib><creatorcontrib>Alberti, Laurent</creatorcontrib><title>Micro‐RNA profiles in osteosarcoma as a predictive tool for ifosfamide response</title><title>International journal of cancer</title><addtitle>Int J Cancer</addtitle><description>Micro‐RNAs (miRNA) are currently used as cancer biomarkers for hematological cancers and solid tumors. Osteosarcoma is the first primary malignant bone tumor, characterized by a complex genetic and resistance to conventional treatments. For this latter property, the median survival has not been improved since 1990 despite preoperative administration of chemotherapeutic agents. The prediction of tumor response before chemotherapy treatment would constitute a major progress for this pathology. We assessed in this study if miRNA profiling could surpass the current limitations for osteosarcoma diagnosis. We measured the miRNA expression in different osteosarcoma samples: (i) 27 osteosarcoma paraffin‐embedded tumors from patients, (ii) human osteosarcoma cell lines, and (iii) tumors from a syngeneic rat osteosarcoma model, recapitulating human osteosarcoma. miRNA profiles were determined using microfluidic cards performing high‐throughput TaqMan®‐based PCR assays, called TaqMan® Low Density Arrays. Osteosarcoma of rat and human origins showed a miRNA signature, which could discriminate good from bad responders. In particular, we identified five discriminating miRNAs (miR‐92a, miR‐99b, miR‐132, miR‐193a‐5p and miR‐422a) in patient tumors, which could be easily transferable to diagnosis. These discriminating miRNAs, as well as those identified in rat, targeted the TGFβ, the Wnt and the MAP kinase pathways. These results indicate that our platform constitutes a potent diagnostic tool to predict tumor sensitivity to a drug in attempt to better adapt treatment to tumor biological specificities and also to identify new potential therapeutic strategies.</description><subject>Animal models</subject><subject>Animals</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>biomarkers</subject><subject>Bone Neoplasms - drug therapy</subject><subject>Bone Neoplasms - genetics</subject><subject>Bone tumors</subject><subject>Cancer</subject><subject>Cell Cycle</subject><subject>Cell Line, Tumor</subject><subject>Chemotherapy</subject><subject>diagnosis</subject><subject>Disease Models, Animal</subject><subject>Diseases of the osteoarticular system</subject><subject>Drugs</subject><subject>Gene Expression Profiling</subject><subject>Humans</subject><subject>Ifosfamide</subject><subject>Ifosfamide - therapeutic use</subject><subject>Life Sciences</subject><subject>MAP kinase</subject><subject>Medical sciences</subject><subject>Microfluidics</subject><subject>MicroRNAs - genetics</subject><subject>MicroRNAs - metabolism</subject><subject>miRNA</subject><subject>miRNA profiling</subject><subject>Neoplasm Invasiveness</subject><subject>Osteosarcoma</subject><subject>Osteosarcoma - drug therapy</subject><subject>Osteosarcoma - genetics</subject><subject>Osteosarcoma cells</subject><subject>Polymerase chain reaction</subject><subject>Rats</subject><subject>Solid tumors</subject><subject>Survival</subject><subject>targeted therapy</subject><subject>Treatment Outcome</subject><subject>Tumors</subject><subject>Tumors of striated muscle and skeleton</subject><subject>Wnt protein</subject><issn>0020-7136</issn><issn>1097-0215</issn><issn>1097-0215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp90c1u1DAQB3ALgehSOPACyBcElUg7duLYOa5W9ANtQSA4W44_hKtkvfXsFvXGI_QZ-yS4zdKe4OTD_DQznj8hrxkcMgB-FC_sIReSiSdkxqCTFXAmnpJZqUElWd3ukReIFwCMCWiekz0OXdOJtpmRr-fR5nT7--bb5zld5xTi4JHGFU248QlNtmk01CA1pepdtJt45ekmpYGGlGkMCYMZo_M0e1ynFfqX5FkwA_pXu3ef_Dj--H1xWi2_nJwt5svKCi5EJWsb7lZwopdKOWF6x5kRUvbcm9DXtlYta_rAoQXLnZN956RveejBsSBFvU8-TH1_mkGvcxxNvtbJRH06X-pYFsmjBi5qrlpxxQp_N_Hyycutx40eI1o_DGbl0xa1alXXCWi7It__V7JyVVWrTkGhBxMtN0TMPjwswkDfRaNLNPo-mmLf7Npu-9G7B_k3iwLe7oBBa4aQzcpGfHQNV6wGXtzR5H6VrK7_PVGffVpMo_8APe6kyQ</recordid><startdate>20110801</startdate><enddate>20110801</enddate><creator>Gougelet, Angélique</creator><creator>Pissaloux, Daniel</creator><creator>Besse, Anthony</creator><creator>Perez, Jennifer</creator><creator>Duc, Adeline</creator><creator>Dutour, Aurélie</creator><creator>Blay, Jean‐Yves</creator><creator>Alberti, Laurent</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Blackwell</general><general>Wiley</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>7TM</scope><scope>7X8</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0002-7686-1750</orcidid><orcidid>https://orcid.org/0000-0001-5741-3576</orcidid><orcidid>https://orcid.org/0000-0001-7190-120X</orcidid></search><sort><creationdate>20110801</creationdate><title>Micro‐RNA profiles in osteosarcoma as a predictive tool for ifosfamide response</title><author>Gougelet, Angélique ; Pissaloux, Daniel ; Besse, Anthony ; Perez, Jennifer ; Duc, Adeline ; Dutour, Aurélie ; Blay, Jean‐Yves ; Alberti, Laurent</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5255-73cf9564d5b788d5abd21a577b2eafb3c38614bf2060c2dd7b9d7e62fb0d1f753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animal models</topic><topic>Animals</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>biomarkers</topic><topic>Bone Neoplasms - drug therapy</topic><topic>Bone Neoplasms - genetics</topic><topic>Bone tumors</topic><topic>Cancer</topic><topic>Cell Cycle</topic><topic>Cell Line, Tumor</topic><topic>Chemotherapy</topic><topic>diagnosis</topic><topic>Disease Models, Animal</topic><topic>Diseases of the osteoarticular system</topic><topic>Drugs</topic><topic>Gene Expression Profiling</topic><topic>Humans</topic><topic>Ifosfamide</topic><topic>Ifosfamide - therapeutic use</topic><topic>Life Sciences</topic><topic>MAP kinase</topic><topic>Medical sciences</topic><topic>Microfluidics</topic><topic>MicroRNAs - genetics</topic><topic>MicroRNAs - metabolism</topic><topic>miRNA</topic><topic>miRNA profiling</topic><topic>Neoplasm Invasiveness</topic><topic>Osteosarcoma</topic><topic>Osteosarcoma - drug therapy</topic><topic>Osteosarcoma - genetics</topic><topic>Osteosarcoma cells</topic><topic>Polymerase chain reaction</topic><topic>Rats</topic><topic>Solid tumors</topic><topic>Survival</topic><topic>targeted therapy</topic><topic>Treatment Outcome</topic><topic>Tumors</topic><topic>Tumors of striated muscle and skeleton</topic><topic>Wnt protein</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gougelet, Angélique</creatorcontrib><creatorcontrib>Pissaloux, Daniel</creatorcontrib><creatorcontrib>Besse, Anthony</creatorcontrib><creatorcontrib>Perez, Jennifer</creatorcontrib><creatorcontrib>Duc, Adeline</creatorcontrib><creatorcontrib>Dutour, Aurélie</creatorcontrib><creatorcontrib>Blay, Jean‐Yves</creatorcontrib><creatorcontrib>Alberti, Laurent</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>Nucleic Acids Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>International journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gougelet, Angélique</au><au>Pissaloux, Daniel</au><au>Besse, Anthony</au><au>Perez, Jennifer</au><au>Duc, Adeline</au><au>Dutour, Aurélie</au><au>Blay, Jean‐Yves</au><au>Alberti, Laurent</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Micro‐RNA profiles in osteosarcoma as a predictive tool for ifosfamide response</atitle><jtitle>International journal of cancer</jtitle><addtitle>Int J Cancer</addtitle><date>2011-08-01</date><risdate>2011</risdate><volume>129</volume><issue>3</issue><spage>680</spage><epage>690</epage><pages>680-690</pages><issn>0020-7136</issn><issn>1097-0215</issn><eissn>1097-0215</eissn><coden>IJCNAW</coden><abstract>Micro‐RNAs (miRNA) are currently used as cancer biomarkers for hematological cancers and solid tumors. Osteosarcoma is the first primary malignant bone tumor, characterized by a complex genetic and resistance to conventional treatments. For this latter property, the median survival has not been improved since 1990 despite preoperative administration of chemotherapeutic agents. The prediction of tumor response before chemotherapy treatment would constitute a major progress for this pathology. We assessed in this study if miRNA profiling could surpass the current limitations for osteosarcoma diagnosis. We measured the miRNA expression in different osteosarcoma samples: (i) 27 osteosarcoma paraffin‐embedded tumors from patients, (ii) human osteosarcoma cell lines, and (iii) tumors from a syngeneic rat osteosarcoma model, recapitulating human osteosarcoma. miRNA profiles were determined using microfluidic cards performing high‐throughput TaqMan®‐based PCR assays, called TaqMan® Low Density Arrays. Osteosarcoma of rat and human origins showed a miRNA signature, which could discriminate good from bad responders. In particular, we identified five discriminating miRNAs (miR‐92a, miR‐99b, miR‐132, miR‐193a‐5p and miR‐422a) in patient tumors, which could be easily transferable to diagnosis. These discriminating miRNAs, as well as those identified in rat, targeted the TGFβ, the Wnt and the MAP kinase pathways. These results indicate that our platform constitutes a potent diagnostic tool to predict tumor sensitivity to a drug in attempt to better adapt treatment to tumor biological specificities and also to identify new potential therapeutic strategies.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>20949564</pmid><doi>10.1002/ijc.25715</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-7686-1750</orcidid><orcidid>https://orcid.org/0000-0001-5741-3576</orcidid><orcidid>https://orcid.org/0000-0001-7190-120X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animal models Animals Antineoplastic Agents - therapeutic use Biological and medical sciences biomarkers Bone Neoplasms - drug therapy Bone Neoplasms - genetics Bone tumors Cancer Cell Cycle Cell Line, Tumor Chemotherapy diagnosis Disease Models, Animal Diseases of the osteoarticular system Drugs Gene Expression Profiling Humans Ifosfamide Ifosfamide - therapeutic use Life Sciences MAP kinase Medical sciences Microfluidics MicroRNAs - genetics MicroRNAs - metabolism miRNA miRNA profiling Neoplasm Invasiveness Osteosarcoma Osteosarcoma - drug therapy Osteosarcoma - genetics Osteosarcoma cells Polymerase chain reaction Rats Solid tumors Survival targeted therapy Treatment Outcome Tumors Tumors of striated muscle and skeleton Wnt protein |
title | Micro‐RNA profiles in osteosarcoma as a predictive tool for ifosfamide response |
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