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Immunolocalization of BRCA1 protein in normal breast tissue and sporadic invasive ductal carcinomas: a correlation with other biological parameters
- Source :
- Histopathology. 34:106-112
- Publication Year :
- 1999
- Publisher :
- Wiley, 1999.
-
Abstract
- Aim BRCA1, a nuclear phosphoprotein, normally functions as a negative regulator of the cell cycle and may be an active inhibitor of neoplastic progression. Mutation of the BRCA1 gene has been demonstrated in 80% of familial breast cancer. Decreased mRNA levels or aberrant subcellular locations of BRCA1 have been identified in breast cancer lines and in sporadic cases of breast cancer tissues. The expression of BRCA1 in large series of variously differentiated breast carcinomas with correlation with other biological parameters has not been clarified. Methods and results The BRCA1 expression in normal breast tissue (n = 15) and in sporadic cases of invasive ductal carcinoma (n = 108) was determined using immunohistochemistry. BRCA1 expression was correlated with other prognostic parameters including p53, c-erbB-2, bcl-2, oestrogen receptor (ER), histological grade, tumour size, axillary lymph node status and age. BRCA1 was exclusively (100%) localized in the nuclei of normal ductal and lobular epithelia. However, this nuclear expression pattern was variable in breast carcinoma (76.8%). Loss of nuclear BRCA1 expression (22 of 108 cases, 20.4%) correlated well with high histological grade (P
- Subjects :
- Pathology
medicine.medical_specialty
Histology
endocrine system diseases
Mammary gland
General Medicine
Biology
medicine.disease
medicine.disease_cause
Pathology and Forensic Medicine
medicine.anatomical_structure
Breast cancer
medicine
Carcinoma
Cancer research
Immunohistochemistry
Sporadic Breast Carcinoma
skin and connective tissue diseases
Breast carcinoma
Carcinogenesis
Lymph node
Subjects
Details
- ISSN :
- 03090167
- Volume :
- 34
- Database :
- OpenAIRE
- Journal :
- Histopathology
- Accession number :
- edsair.doi...........e8a725bfe173c9ffd718cd3d64537d0d
- Full Text :
- https://doi.org/10.1046/j.1365-2559.1999.00578.x