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Identification of novel candidate circulating biomarkers for malignant soft tissue sarcomas: Correlation with metastatic progression.
Conti, Amalia; Fredolini, Claudia; Tamburro, Davide; Magagnoli, Giovanna; Zhou, Weidong; Liotta, Lance A; Picci, Piero; Luchini, Alessandra; Benassi, Maria Serena.
Afiliación
  • Conti A; Laboratory of Experimental Oncology, Istituto Ortopedico Rizzoli, Bologna, Italy.
  • Fredolini C; Center for Applied Proteomics and Molecular Medicine, George Mason University, Manassas, VA, USA.
  • Tamburro D; Center for Applied Proteomics and Molecular Medicine, George Mason University, Manassas, VA, USA.
  • Magagnoli G; Center for Applied Proteomics and Molecular Medicine, George Mason University, Manassas, VA, USA.
  • Zhou W; Laboratory of Experimental Oncology, Istituto Ortopedico Rizzoli, Bologna, Italy.
  • Liotta LA; Center for Applied Proteomics and Molecular Medicine, George Mason University, Manassas, VA, USA.
  • Picci P; Center for Applied Proteomics and Molecular Medicine, George Mason University, Manassas, VA, USA.
  • Luchini A; Laboratory of Experimental Oncology, Istituto Ortopedico Rizzoli, Bologna, Italy.
  • Benassi MS; Center for Applied Proteomics and Molecular Medicine, George Mason University, Manassas, VA, USA.
Proteomics ; 16(4): 689-97, 2016 Feb.
Article en En | MEDLINE | ID: mdl-26699407
ABSTRACT
Soft tissue sarcomas (STS) are a heterogeneous group of rare tumors for which identification and validation of biological markers may improve clinical management. The fraction of low-molecular-weight (LMW) circulating proteins and fragments of proteins is a rich source of new potential biomarkers. To identify circulating biomarkers useful for STS early diagnosis and prognosis, we analyzed 53 high-grade STS sera using hydrogel core-shell nanoparticles that selectively entrap LMW proteins by size exclusion and affinity chromatography, protect them from degradation and amplify their concentration for mass spectrometry detection. Twenty-two analytes mostly involved in inflammatory and immunological response, showed a progressive increase from benign to malignant STS with a relative difference in abundance, more than 50% when compared to healthy control. 16 of these were higher in metastatic compared to non-metastatic tumors. Cox's regression analysis revealed a statistical significant association between the abundance of lactotransferrin (LTF) and complement factor H-related 5 (CFHR5) and risk of metastasis. In particular, CFHR5 was associated with the risk of metastasis. The role of circulating proteins involved in metastatic progression will be crucial for a better understanding of STS biology and patient management.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Sarcoma / Proteínas Sanguíneas Tipo de estudio: Diagnostic_studies / Prognostic_studies / Screening_studies Límite: Humans Idioma: En Revista: Proteomics Asunto de la revista: BIOQUIMICA Año: 2016 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Sarcoma / Proteínas Sanguíneas Tipo de estudio: Diagnostic_studies / Prognostic_studies / Screening_studies Límite: Humans Idioma: En Revista: Proteomics Asunto de la revista: BIOQUIMICA Año: 2016 Tipo del documento: Article País de afiliación: Italia