BACKGROUND: In patients with cancer, circulating endothelial cells (CECs) are increased and are correlated with an aggressive disease course. However, the clinical and biologic significance of CECs in chronic lymphocytic leukemia (CLL) remains uncertain. METHODS: In 170 patients with CLL, CEC levels were quantified by flow cytometry and were correlated with clinical and biologic data. In addition, CECs were characterized by immunophenotypic, fluorescence in situ hybridization (FISH), and gene expression profile analyses. RESULTS: In patients with CLL, CECs were increased compared with controls. A higher level of CECs (>20/microL) identified a subset of patients with a more aggressive disease course characterized by a shorter time to first treatment both in univariate and multivariate analyses. In FISH analysis, 7 patients had a significant proportion of CECs and presented with the same cytogenetic lesion of neoplastic lymphocytes and immunophenotypic features of endothelial progenitor cells. The gene expression profile of sorted CECs revealed a molecular pattern, suggesting a derivation from CLL leukemic cells with increased cell survival and proliferation, diminished cell adhesion to extracellular matrix, and enhanced proangiogenic function compared with their normal counterparts. CONCLUSIONS: The current data suggest that, in CLL, CECs may represent a biologic marker of aggressiveness and disease progression to be considered for new, targeted antiangiogenic treatments. (c) 2010 American Cancer Society.
BACKGROUND: In patients with cancer, circulating endothelial cells (CECs) are increased and are correlated with an aggressive disease course. However, the clinical and biologic significance of CECs in chronic lymphocytic leukemia (CLL) remains uncertain. METHODS: In 170 patients with CLL, CEC levels were quantified by flow cytometry and were correlated with clinical and biologic data. In addition, CECs were characterized by immunophenotypic, fluorescence in situ hybridization (FISH), and gene expression profile analyses. RESULTS: In patients with CLL, CECs were increased compared with controls. A higher level of CECs (>20/microL) identified a subset of patients with a more aggressive disease course characterized by a shorter time to first treatment both in univariate and multivariate analyses. In FISH analysis, 7 patients had a significant proportion of CECs and presented with the same cytogenetic lesion of neoplastic lymphocytes and immunophenotypic features of endothelial progenitor cells. The gene expression profile of sorted CECs revealed a molecular pattern, suggesting a derivation from CLL leukemic cells with increased cell survival and proliferation, diminished cell adhesion to extracellular matrix, and enhanced proangiogenic function compared with their normal counterparts. CONCLUSIONS: The current data suggest that, in CLL, CECs may represent a biologic marker of aggressiveness and disease progression to be considered for new, targeted antiangiogenic treatments. (c) 2010 American Cancer Society.
Authors: F M Rossi; A Zucchetto; E Tissino; M Dal Bo; R Bomben; C Caldana; F Pozzo; G Del Poeta; D Rossi; G Gaidano; V Gattei Journal: Leukemia Date: 2013-11-08 Impact factor: 11.528
Authors: Manuela Ferracin; Barbara Zagatti; Lara Rizzotto; Francesco Cavazzini; Angelo Veronese; Maria Ciccone; Elena Saccenti; Laura Lupini; Andrea Grilli; Cristiano De Angeli; Massimo Negrini; Antonio Cuneo Journal: Mol Cancer Date: 2010-05-26 Impact factor: 27.401
Authors: Gian Matteo Rigolin; Elena Saccenti; Lara Rizzotto; Manuela Ferracin; Sara Martinelli; Luca Formigaro; Francesca Cibien; Maurizio Cavallari; Enrico Lista; Giulia Daghia; Olga Sofritti; Maria Ciccone; Francesco Cavazzini; Laura Lupini; Cristian Bassi; Barbara Zagatti; Massimo Negrini; Antonio Cuneo Journal: Oncotarget Date: 2014-01-15
Authors: Gian Matteo Rigolin; Luca Formigaro; Maurizio Cavallari; Francesca Maria Quaglia; Enrico Lista; Antonio Urso; Emanuele Guardalben; Sara Martinelli; Elena Saccenti; Cristian Bassi; Laura Lupini; Maria Antonella Bardi; Eleonora Volta; Elisa Tammiso; Aurora Melandri; Massimo Negrini; Francesco Cavazzini; Antonio Cuneo Journal: Oncotarget Date: 2017-04-25
Authors: Antonio Cuneo; Francesco Cavazzini; Maria Ciccone; Giulia Daghia; Olga Sofritti; Elena Saccenti; Massimo Negrini; Gian Matteo Rigolin Journal: Cancer Med Date: 2014-03-19 Impact factor: 4.452