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Loss of progesterone receptor is associated with distinct tyrosine kinase profiles in breast cancer.
Tahiri, Andliena; Tekpli, Xavier; Satheesh, Somisetty V; DeWijn, Rik; Lüders, Torben; Bukholm, Ida R; Hurtado, Antoni; Geisler, Jürgen; Kristensen, Vessela N.
Afiliação
  • Tahiri A; Department of Clinical Molecular Biology (EpiGen), Akershus University Hospital, Lørenskog, Norway.
  • Tekpli X; Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
  • Satheesh SV; Department of Medical Genetics, Oslo University Hospital, Oslo, Norway.
  • DeWijn R; Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
  • Lüders T; Hamilton Nordics, Slattum, Norway.
  • Bukholm IR; PamGene International B.V., 's-Hertogenbosch, The Netherlands.
  • Hurtado A; Department of Clinical Molecular Biology (EpiGen), Akershus University Hospital, Lørenskog, Norway.
  • Geisler J; Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
  • Kristensen VN; Helgelandssykehuset HF and Norwegian University of Life Sciences (NMBU), Ås, Norway.
Breast Cancer Res Treat ; 183(3): 585-598, 2020 Oct.
Article em En | MEDLINE | ID: mdl-32710281
PURPOSE: The aim of this study was to assess protein tyrosine kinase profiles in primary breast cancer samples in correlation with the distinct hormone and growth receptor profiles ER, PR, and HER2. EXPERIMENTAL DESIGN: Pamchip® microarrays were used to measure the phosphorylation of 144 tyrosine kinase substrates in 29 ER+ breast cancer samples and cell lines MCF7, BT474 and ZR75-1. mRNA expression data from the METABRIC cohort and publicly available PR chip-sequencing data were used for validation purposes, together with RT-PCR. RESULTS: In ER+ breast tumors and cell lines, we observed that the loss of PR expression correlated to higher kinase activity in samples and cell lines that were HER2-. A number of kinases, representing mostly proteins within the PI3K/AKT pathway, were identified as responsible for the differential phosphorylation between PR- and PR+ in ER+/HER2- tumors. We used the METABRIC cohort to analyze mRNA expression from 977 ER+/HER2- breast cancers. Twenty four kinase-encoding genes were identified as differentially expressed between PR+ and PR-, dividing ER+/HER2- samples in two distinct clusters with significant differences in survival (p < 0.05). Four kinase genes, LCK, FRK, FGFR4, and MST1R, were identified as potential direct targets of PR. CONCLUSIONS: Our results suggest that the PR status has a profound effect on tyrosine kinases, especially for FGFR4 and LCK genes, in ER+/HER2- breast cancer patients. The influence of these genes on the PI3K/AKT signaling pathway may potentially lead to novel drug targets for ER+/PR- breast cancer patients.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Receptores de Progesterona Tipo de estudo: Risk_factors_studies Limite: Female / Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Receptores de Progesterona Tipo de estudo: Risk_factors_studies Limite: Female / Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article