Purpose: Patients with benign breast biopsies that exit atypical epithelial proliferation or fibroadenoma may be at increased risk for invasive breast cancer. We hypothesized that molecular markers might also be use-ful to evaluate the malignant potential of nonneoplastic breast tissue. Patients and Methods: Study subjects belonged to a cohort of 6,805 women who underwent biopsy for non-malignant breast disease at the Mayo Clinic and Roches-ter-affiliated hospitals between 1967 and 1981. As part of a nested case-control study that compared subjects who developed invasive breast cancer with those who did not, we analyzed a sample of 60 benign breast biops-ies for the following markers: HER-2/neu and p53 over-expression by immunohistochemistr...
AbstractAberrations of p53 occur in most, if not all, human cancers. In breast cancer, p53 mutation ...
Background: Fibrocystic changes are associated with an increased risk of breast cancer. Genetic alte...
Introduction The Li–Fraumeni Syndrome is caused by a germline TP53 mutation and is associated with a...
Mutations in p53 exons 5-8 are found in 40-50% of breast carcinomas. We performed a retrospective an...
To achieve a more accurate diagnosis in the first aspiration biopsy from breast tumor, p53 gene muta...
Breast cancer cells can be obtained derectly from the patient with minimal damage by fine-needle sam...
Mutations of the p53 gene play a key role in the development of common human malignancies. In the ca...
Benign breast diseases are both common and heterogeneous. Some types (usual and atypical hyperplasia...
Abstract Background Benign breast disease (BBD) is a risk factor for breast cancer (BC); however, li...
Germline mutations at BRCA1 or BRCA2 genes result in susceptibility to breast and ovarian cancers. B...
Aberrations of p53 occur in most, if not all, human cancers. In breast cancer, p53 mutation is the m...
Accumulation of p53 protein resulting in levels detectable by immunohistochemistry (IHC) has been pr...
Breast cancer is a polymorphic disease and, until now, nodal invasion and steroid receptor levels re...
ABSTRACT: BACKGROUND: Basal-like breast cancers (BLBC) are aggressive breast cancers for which, so f...
Overexpression of the nuclear phosphoprotein p53 is one of the most frequently detected abnormalitie...
AbstractAberrations of p53 occur in most, if not all, human cancers. In breast cancer, p53 mutation ...
Background: Fibrocystic changes are associated with an increased risk of breast cancer. Genetic alte...
Introduction The Li–Fraumeni Syndrome is caused by a germline TP53 mutation and is associated with a...
Mutations in p53 exons 5-8 are found in 40-50% of breast carcinomas. We performed a retrospective an...
To achieve a more accurate diagnosis in the first aspiration biopsy from breast tumor, p53 gene muta...
Breast cancer cells can be obtained derectly from the patient with minimal damage by fine-needle sam...
Mutations of the p53 gene play a key role in the development of common human malignancies. In the ca...
Benign breast diseases are both common and heterogeneous. Some types (usual and atypical hyperplasia...
Abstract Background Benign breast disease (BBD) is a risk factor for breast cancer (BC); however, li...
Germline mutations at BRCA1 or BRCA2 genes result in susceptibility to breast and ovarian cancers. B...
Aberrations of p53 occur in most, if not all, human cancers. In breast cancer, p53 mutation is the m...
Accumulation of p53 protein resulting in levels detectable by immunohistochemistry (IHC) has been pr...
Breast cancer is a polymorphic disease and, until now, nodal invasion and steroid receptor levels re...
ABSTRACT: BACKGROUND: Basal-like breast cancers (BLBC) are aggressive breast cancers for which, so f...
Overexpression of the nuclear phosphoprotein p53 is one of the most frequently detected abnormalitie...
AbstractAberrations of p53 occur in most, if not all, human cancers. In breast cancer, p53 mutation ...
Background: Fibrocystic changes are associated with an increased risk of breast cancer. Genetic alte...
Introduction The Li–Fraumeni Syndrome is caused by a germline TP53 mutation and is associated with a...