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J Clin Pathol ; 60(4): 397-404, 2007 Apr.
Article in English | MEDLINE | ID: mdl-16775123

ABSTRACT

AIM: To assess whether immunohistochemically stained tissue microarrays (TMA) of 2 mm cores from paraffin embedded tumour tissue may replace whole sections in semi-quantitative evaluation of selected potential markers for endocrine treatment. METHODS: Whole sections and 2 mm cores on TMA were used for immunohistochemical staining of potential markers for endocrine treatment. The Allred scoring system was used for the markers with nuclear localisation: the oestrogen receptor, the progesterone receptor, p27 and the oestrogen receptor co-regulator amplified in breast cancer 1 (AIB1). The Allred scoring system was also used for the non-nuclear markers Bcl-2, pS2 and cyclooxygenase 2 (COX-2); the membrane receptors HER-2, insulin-like growth factor I receptor (IGF-IR) and epidermal growth factor receptor were quantified according to the guidelines for the Herceptest. RESULTS: The data and statistical analyses showed that the semi-quantitative evaluation of oestrogen receptor, progesterone receptor, AIB1, COX-2, HER-2 and IGF-IR on TMA blocks was comparable with analysis on whole sections. CONCLUSIONS: This study shows that semi-quantitative scoring of 2 mm cores on TMA is feasible for several potential markers for endocrine therapy. Considering the small size of many breast tumours, the speed and cost-effectiveness of immunohistochemistry on TMA compared with whole sections, and the importance of the expression level of the proteins, semi-quantitative scoring on TMA has great potential in both retrospective and prospective studies aiming at improving the prediction of response to endocrine treatment.


Subject(s)
Antineoplastic Agents, Hormonal/therapeutic use , Biomarkers, Tumor/analysis , Breast Neoplasms/chemistry , Neoplasm Proteins/analysis , Breast Neoplasms/drug therapy , Cell Membrane/chemistry , Cell Nucleus/chemistry , Cyclooxygenase 2/analysis , Cytoplasm/chemistry , Female , Histone Acetyltransferases/analysis , Humans , Immunoenzyme Techniques , Nuclear Receptor Coactivator 3 , Receptor, ErbB-2/analysis , Receptor, IGF Type 1/analysis , Receptors, Estrogen/analysis , Receptors, Progesterone/analysis , Specimen Handling/methods , Tamoxifen/therapeutic use , Tissue Array Analysis/methods , Trans-Activators/analysis
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