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FKBPL: a marker of good prognosis in breast cancer.
Nelson, Laura; McKeen, Hayley D; Marshall, Andrea; Mulrane, Laoighse; Starczynski, Jane; Storr, Sarah J; Lanigan, Fiona; Byrne, Christopher; Arthur, Ken; Hegarty, Shauna; Ali, Ahlam Abdunnabi; Furlong, Fiona; McCarthy, Helen O; Ellis, Ian O; Green, Andrew R; Rakha, Emad; Young, Leonie; Kunkler, Ian; Thomas, Jeremy; Jack, Wilma; Cameron, David; Jirström, Karin; Yakkundi, Anita; McClements, Lana; Martin, Stewart G; Gallagher, William M; Dunn, Janet; Bartlett, John; O'Connor, Darran; Robson, Tracy.
Afiliación
  • Nelson L; School of Pharmacy, Queen's University Belfast, Belfast, United Kingdom.
  • McKeen HD; School of Pharmacy, Queen's University Belfast, Belfast, United Kingdom.
  • Marshall A; Warwick Clinical Trials Unit, University of Warwick, Coventry, United Kingdom.
  • Mulrane L; Conway Institute, University College Dublin, Dublin, Ireland.
  • Starczynski J; Ontario Institute for Cancer Research, Toronto, Canada.
  • Storr SJ; Division of Cancer and Stem Cells, School of Medicine, University of Nottingham, Nottingham, United Kingdom.
  • Lanigan F; Conway Institute, University College Dublin, Dublin, Ireland.
  • Byrne C; Royal College of Surgeons Ireland, Dublin, Ireland.
  • Arthur K; Northern Ireland Molecular Pathology Laboratory, CCRCB, Queens University Belfast, Belfast, United Kingdom.
  • Hegarty S; Department of Pathology, Royal Group of Hospitals, Grosvenor Road, Belfast, United Kingdom.
  • Ali AA; School of Pharmacy, Queen's University Belfast, Belfast, United Kingdom.
  • Furlong F; School of Pharmacy, Queen's University Belfast, Belfast, United Kingdom.
  • McCarthy HO; School of Pharmacy, Queen's University Belfast, Belfast, United Kingdom.
  • Ellis IO; Division of Cancer and Stem Cells, School of Medicine, University of Nottingham, Nottingham, United Kingdom.
  • Green AR; Division of Cancer and Stem Cells, School of Medicine, University of Nottingham, Nottingham, United Kingdom.
  • Rakha E; Division of Cancer and Stem Cells, School of Medicine, University of Nottingham, Nottingham, United Kingdom.
  • Young L; Royal College of Surgeons Ireland, Dublin, Ireland.
  • Kunkler I; Edinburgh Breast Unit, The University of Edinburgh, Edinburgh, United Kingdom.
  • Thomas J; Edinburgh Breast Unit, The University of Edinburgh, Edinburgh, United Kingdom.
  • Jack W; Edinburgh Breast Unit, The University of Edinburgh, Edinburgh, United Kingdom.
  • Cameron D; Edinburgh Breast Unit, The University of Edinburgh, Edinburgh, United Kingdom.
  • Jirström K; Department of Clinical Sciences, Lund University, Sweden.
  • Yakkundi A; School of Pharmacy, Queen's University Belfast, Belfast, United Kingdom.
  • McClements L; School of Pharmacy, Queen's University Belfast, Belfast, United Kingdom.
  • Martin SG; Division of Cancer and Stem Cells, School of Medicine, University of Nottingham, Nottingham, United Kingdom.
  • Gallagher WM; Conway Institute, University College Dublin, Dublin, Ireland.
  • Dunn J; Warwick Clinical Trials Unit, University of Warwick, Coventry, United Kingdom.
  • Bartlett J; Ontario Institute for Cancer Research, Toronto, Canada.
  • O'Connor D; Edinburgh Cancer Research Centre, The University of Edinburgh, Edinburgh, United Kingdom.
  • Robson T; Conway Institute, University College Dublin, Dublin, Ireland.
Oncotarget ; 6(14): 12209-23, 2015 May 20.
Article en En | MEDLINE | ID: mdl-25906750
ABSTRACT
FK506-binding protein-like (FKBPL) has established roles as an anti-tumor protein, with a therapeutic peptide based on this protein, ALM201, shortly entering phase I/II clinical trials. Here, we evaluated FKBPL's prognostic ability in primary breast cancer tissue, represented on tissue microarrays (TMA) from 3277 women recruited into five independent retrospective studies, using immunohistochemistry (IHC). In a meta-analysis, FKBPL levels were a significant predictor of BCSS; low FKBPL levels indicated poorer breast cancer specific survival (BCSS) (hazard ratio (HR) = 1.30, 95% confidence interval (CI) 1.14-1.49, p < 0.001). The prognostic impact of FKBPL remained significant after adjusting for other known prognostic factors (HR = 1.25, 95% CI 1.07-1.45, p = 0.004). For the sub-groups of 2365 estrogen receptor (ER) positive patients and 1649 tamoxifen treated patients, FKBPL was significantly associated with BCSS (HR = 1.34, 95% CI 1.13-1.58, p < 0.001, and HR = 1.25, 95% CI 1.04-1.49, p = 0.02, respectively). A univariate analysis revealed that FKBPL was also a significant predictor of relapse free interval (RFI) within the ER positive patient group, but it was only borderline significant within the smaller tamoxifen treated patient group (HR = 1.32 95% CI 1.05-1.65, p = 0.02 and HR = 1.23 95% CI 0.99-1.54, p = 0.06, respectively). The data suggests a role for FKBPL as a prognostic factor for BCSS, with the potential to be routinely evaluated within the clinic.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias de la Mama / Inmunofilinas Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Female / Humans Idioma: En Revista: Oncotarget Año: 2015 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias de la Mama / Inmunofilinas Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Female / Humans Idioma: En Revista: Oncotarget Año: 2015 Tipo del documento: Article País de afiliación: Reino Unido