Evaluation of Endoglin (CD105) expression in pediatric rhabdomyosarcoma

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 specif...

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Veröffentlicht in:BMC cancer 2018-01, Vol.18 (1), p.31-31, Article 31
Hauptverfasser: Di Paolo, Virginia, Russo, Ida, Boldrini, Renata, Ravà, Lucilla, Pezzullo, Marco, Benedetti, Maria Chiara, Galardi, Angela, Colletti, Marta, Rota, Rossella, Orlando, Domenico, Crocoli, Alessandro, Peinado, Hector, Milano, Giuseppe Maria, Di Giannatale, Angela
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Sprache:eng
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Zusammenfassung: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. 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. 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 
ISSN:1471-2407
1471-2407
DOI:10.1186/s12885-017-3947-4