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Prognostic impact of total and tyrosine phosphorylated GIV/Girdin in breast cancers.
Dunkel, Ying; Diao, Kexin; Aznar, Nicolas; Swanson, Lee; Liu, Lawrence; Zhu, Wenhong; Mi, Xiao-Yi; Ghosh, Pradipta.
Afiliação
  • Dunkel Y; Department of Medicine.
  • Diao K; Department of Cell and Molecular Medicine.
  • Aznar N; Department of Pathology, China Medical University, Shenyang, China.
  • Swanson L; Department of Medicine.
  • Liu L; Department of Cell and Molecular Medicine.
  • Zhu W; Department of Medicine.
  • Mi XY; Department of Cell and Molecular Medicine.
  • Ghosh P; Department of Medicine.
FASEB J ; 30(11): 3702-3713, 2016 11.
Article em En | MEDLINE | ID: mdl-27440794
ABSTRACT
Gα-interacting vesicle-associated protein (GIV, aka Girdin) is a guanine exchange factor (GEF) for the trimeric G protein Gαi and a bona fide metastasis-related gene that serves as a platform for amplification of tyrosine-based signals via G-protein intermediates. Here we present the first exploratory biomarker study conducted on a cohort of 187 patients with breast cancer to evaluate the prognostic role of total GIV (tGIV) and tyrosine phosphorylated GIV (pYGIV) across the various molecular subtypes. A Kaplan-Meier analysis of recurrence-free survival showed that the presence of tGIV, either cytoplasmic or nuclear, carried poor prognosis, but that nuclear tGIV had a greater prognostic impact (P = 0.007 in early and P = 0.0048 in late clinical stages). Activated pYGIV in the cytoplasm had the greatest prognostic impact in late clinical stages (P = 0.006). Furthermore, we found that the prognostic impacts of cytoplasmic pYGIV and nuclear tGIV were additive (hazard ratio 19.0548; P = 0.0002). Surprisingly, this additive effect of nuclear tGIV/cytoplasmic pYGIV was observed in human epidermal growth factor receptor 2-positive tumors (hazard ratio 16.918; P = 0.0005) but not in triple-negative breast cancers. In triple-negative breast cancers, tGIV and cytoplasmic pYGIV had no prognostic impact; however, membrane-association of pYGIV carried a poor prognosis (P = 0.026). Both tGIV and pYGIV showed no correlation with clinical stage, tumor size, pathologic type, lymph node involvement, and BRCA1/2 status. We conclude that immunocytochemical detection of pYGIV and tGIV can serve as an effective prognosticator. On the basis of the differential prognostic impact of tGIV/pYGIV within each molecular subtype, we propose a diagnostic algorithm. Further studies on larger cohorts are essential to rigorously assess the effectiveness and robustness of this algorithm in prognosticating outcome among patients with breast cancer.-Dunkel, Y., Diao, K., Aznar, N., Swanson, L., Liu, L., Zhu, W., Mi, X.-Y., Ghosh, P. Prognostic impact of total and tyrosine phosphorylated GIV/Girdin in breast cancers.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Tirosina / Neoplasias da Mama / Proteínas de Transporte Vesicular / Proteínas dos Microfilamentos Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adult / Aged / Female / Humans / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Tirosina / Neoplasias da Mama / Proteínas de Transporte Vesicular / Proteínas dos Microfilamentos Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adult / Aged / Female / Humans / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article