%0 Journal Article
%T Clinical relevance of ErbB-2/HER2 nuclear expression in breast cancer
%A Roxana Schillaci
%A Pablo Guzm¨¢n
%A Florencia Cayrol
%A Wendy Beguelin
%A Mar¨ªa C D¨ªaz Flaqu¨¦
%A Cecilia J Proietti
%A Viviana Pineda
%A Jorge Palazzi
%A Isabel Frahm
%A Eduardo H Charreau
%A Esteban Maronna
%A Juan C Roa
%A Patricia V Elizalde
%J BMC Cancer
%D 2012
%I BioMed Central
%R 10.1186/1471-2407-12-74
%X Tissue microarrays from a cohort of 273 primary invasive breast carcinomas from women living in Chile, a Latin American country, were examined for membrane (MembErbB-2) and NuclErbB-2 expression by an immunofluorescence (IF) protocol we developed. ErbB-2 expression was also evaluated by immunohistochemistry (IHC) with a series of antibodies. Correlation between NuclErbB-2 and MembErbB-2, and between NuclErbB-2 and clinicopathological characteristics of tumors was studied. The prognostic value of NuclErbB-2 in overall survival (OS) was evaluated using Kaplan-Meier method, and Cox model was used to explore NuclErbB-2 as independent prognostic factor for OS.The IF protocol we developed showed significantly higher sensitivity for detection of NuclErbB-2 than IHC procedures, while its specificity and sensitivity to detect MembErbB-2 were comparable to those of IHC procedures. We found 33.6% NuclErbB-2 positivity, 14.2% MembErbB-2 overexpression by IF, and 13.0% MembErbB-2 prevalence by IHC in our cohort. We identified NuclErbB-2 positivity as a significant independent predictor of worse OS in patients with MembErbB-2 overexpression. NuclErbB-2 was also a biomarker of lower OS in tumors that overexpress MembErbB-2 and lack steroid hormone receptors.We revealed a novel role for NuclErbB-2 as an independent prognostic factor of poor clinical outcome in MembErbB-2-positive breast tumors. Our work indicates that patients presenting NuclErbB-2 may need new therapeutic strategies involving specific blockage of ErbB-2 nuclear migration.Human epidermal growth factor receptor 2 (ErbB-2/HER2), one of the members of the ErbB family of membrane receptor tyrosine kinases, is a major player in the breast cancer scenario [1]. Membrane ErbB-2 (MembErbB-2) overexpression is associated with poor clinical outcome [2]. At present, the recombinant humanized anti-ErbB-2 monoclonal antibody trastuzumab is successfully used for treatment of MembErbB-2-positive breast cancer in the metastatic and
%U http://www.biomedcentral.com/1471-2407/12/74