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C-Kit receptor and tryptase expressing mast cells correlate with angiogenesis in breast cancer patients

C-Kit protein is a transmembrane tyrosine kinase (TK) receptor (c-KitR-TK), which is predominantly expressed on mast cells (MCs) playing a role in tumor angiogenesis. It could be also expressed on epithelial breast cancer cells (EBCCs), but no data have been published regarding the correlation betwe...

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Detalles Bibliográficos
Autores principales: Marech, Ilaria, Ammendola, Michele, Leporini, Christian, Patruno, Rosa, Luposella, Maria, Zizzo, Nicola, Passantino, Giuseppe, Sacco, Rosario, Farooqi, Ammad Ahmad, Zuccalà, Valeria, Leo, Silvana, Dentamaro, Rosalba, Porcelli, Mariangela, Gadaleta, Pietro, De Sarro, Giovambattista, Gadaleta, Cosmo Damiano, Ranieri, Girolamo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5814269/
https://www.ncbi.nlm.nih.gov/pubmed/29487702
http://dx.doi.org/10.18632/oncotarget.23722
Descripción
Sumario:C-Kit protein is a transmembrane tyrosine kinase (TK) receptor (c-KitR-TK), which is predominantly expressed on mast cells (MCs) playing a role in tumor angiogenesis. It could be also expressed on epithelial breast cancer cells (EBCCs), but no data have been published regarding the correlation between mast cells positive to c-KitR (MCs-c-KitR), EBCCs positive to c-KitR (EBCCs-c-KitR), BC angiogenesis in terms of microvessel density (MVD) and the main clinic-pathological features. This study aims to evaluate the above parameters and their correlations in a series of selected 121 female early BC patients. It has been found a strong correlation between MVD and MCDPT, and MCs-c-KitR, MVD and MCs density positive to tryptase (MCDPT), and MCs-c-KitR and MCDPT by Pearson correlation. These data suggest an involvement of both MCDPT and MCs-c-KitR in BC tumor angiogenesis. Furthermore, BC tissue expressing c-KitR could be a putative predictive factor to c-KitR-TK inhibitors. In this way, selected patients with higher MCs-c-KitR could be candidate to receive c-KitR-TK inhibitors (e.g. masitinib, sunitinib) or tryptase inhibitors (e.g. nafamostat mesilate, gabexate mesilate).