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dc.contributor.authorDi Paolo, Virginia
dc.contributor.authorRusso, Ida
dc.contributor.authorBoldrini, Renata
dc.contributor.authorRavà, Lucilla
dc.contributor.authorPezzullo, Marco
dc.contributor.authorBenedetti, Maria Chiara
dc.contributor.authorGalardi, Angela
dc.contributor.authorColletti, Marta
dc.contributor.authorRota, Rossella
dc.contributor.authorOrlando, Domenico
dc.contributor.authorCrocoli, Alessandro
dc.contributor.authorPeinado Selgas , Hector 
dc.contributor.authorMilano, Giuseppe Maria
dc.contributor.authorDi Giannatale, Angela
dc.date.accessioned2018-11-16T13:00:47Z
dc.date.available2018-11-16T13:00:47Z
dc.date.issued2018
dc.identifier.citationBMC Cancer.(2018); 18(1):31.es_ES
dc.identifier.issn1471-2407es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/6623
dc.description.abstractBACKGROUND: The Intratumoral Microvessel Density (IMVD) is commonly used to quantify tumoral vascularization and is usually assessed by pan-endothelial markers, such as CD31. Endoglin (CD105) is a protein predominantly expressed in proliferating endothelium and the IMVD determined by this marker measures specifically the neovascularization. In this study, we investigated the CD105 expression in pediatric rhabdomyosarcoma and assessed the neovascularization by using the angiogenic ratio IMVD-CD105 to IMVD-CD31. METHODS: Paraffin-embedded archival tumor specimens were selected from 65 pediatric patients affected by rhabdomyosarcoma. The expression levels of CD105, CD31 and Vascular Endothelial Growth Factor (VEGF) were investigated in 30 cases (18 embryonal and 12 alveolar) available for this study. The IMVD-CD105 to IMVD-CD31 expression ratio was correlated with clinical and pathologic features of these patients. RESULTS: We found a specific expression of endoglin (CD105) in endothelial cells of all the rhabdomyosarcoma specimens analyzed. We observed a significant positive correlation between the IMVD individually measured by CD105 and CD31. The CD105/CD31 expression ratio was significantly higher in patients with lower survival and embryonal histology. Indeed, patients with a CD105/CD31 expression ratio < 1.3 had a significantly increased OS (88%, 95%CI, 60%-97%) compared to patients with higher values (40%, 95%CI, 12%-67%). We did not find any statistical correlation among VEGF and EFS, OS and CD105/CD31 expression ratio. CONCLUSION: CD105 is expressed on endothelial cells of rhabdomyosarcoma and represent a useful tool to quantify neovascularization in this tumor. If confirmed by further studies, these results will indicate that CD105 is a potential target for combined therapies in rhabdomyosarcoma.es_ES
dc.description.sponsorshipWe thank Professor Franco Locatelli for critical reading this paper and for his suggestions. We would also like to thank the children ’ s parents, who gave their informed consent for publication and “Il cuore grande di Flavio ”Onlus. Dr. Marta Colletti is a post-doctoral fellow of the Umberto Veronesi Founda- tion. To Valentina Polcini for proofreading.es_ES
dc.language.isoenges_ES
dc.publisherBioMed Central (BMC) es_ES
dc.type.hasVersionVoRes_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectCD105/CD31 ratioes_ES
dc.subjectEndoglin (CD105)es_ES
dc.subjectPrognostic markeres_ES
dc.subjectRhabdomyosarcomaes_ES
dc.subject.meshAdolescent es_ES
dc.subject.meshBiomarkers, Tumor es_ES
dc.subject.meshChild es_ES
dc.subject.meshChild, Preschool es_ES
dc.subject.meshDisease-Free Survival es_ES
dc.subject.meshEndoglin es_ES
dc.subject.meshFemale es_ES
dc.subject.meshGene Expression Regulation, Neoplastic es_ES
dc.subject.meshHumans es_ES
dc.subject.meshInfant es_ES
dc.subject.meshInfant, Newborn es_ES
dc.subject.meshMale es_ES
dc.subject.meshNeovascularization, Pathologices_ES
dc.subject.meshPlatelet Endothelial Cell Adhesion Molecule-1 es_ES
dc.subject.meshRhabdomyosarcoma es_ES
dc.subject.meshVascular Endothelial Growth Factor A es_ES
dc.titleEvaluation of Endoglin (CD105) expression in pediatric rhabdomyosarcomaes_ES
dc.typejournal articlees_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.identifier.pubmedID29304781es_ES
dc.format.volume18es_ES
dc.format.number1es_ES
dc.format.page31es_ES
dc.identifier.doi10.1186/s12885-017-3947-4es_ES
dc.description.peerreviewed
dc.identifier.e-issn1471-2407es_ES
dc.relation.publisherversionhttps://doi.org/10.1186/s12885-017-3947-4.es_ES
dc.identifier.journalBMC canceres_ES
dc.repisalud.institucionCNIOes_ES
dc.repisalud.orgCNIOCNIO::Grupos de investigación::Grupo de Microambiente y Metástasises_ES
dc.rights.accessRightsopen accesses_ES


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Atribución 4.0 Internacional
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