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PMID: 16033833 已发表 · ppublish 英语

Prediction of BRCA1 status in patients with breast cancer using estrogen receptor and basal phenotype.

Lakhani Sunil R, Reis-Filho Jorge S, Fulford Laura, Penault-Llorca Frederique, van der Vijver Marc, Parry Suzanne, Bishop Timothy, Benitez Javier, Rivas Carmen, Bignon Yves-Jean, Chang-Claude Jenny, Hamann Ute, Cornelisse Cees J, Devilee Peter, Beckmann Matthias W, Nestle-Krämling Carolin, Daly Peter A, Haites Neva, Varley Jenny, Lalloo Fiona, Evans Gareth, Maugard Christine, Meijers-Heijboer Hanne, Klijn Jan G M, Olah Edith, Gusterson Barry A, Pilotti Silvana, Radice Paolo, Scherneck Siegfried, Sobol Hagay, Jacquemier Jocelyne, Wagner Teresa, Peto Julian, Stratton Michael R, McGuffog Lesley, Easton Douglas F,

摘要

To investigate the proportion of breast cancers arising in patients with germ line BRCA1 and BRCA2 mutations expressing basal markers and developing predictive tests for identification of high-risk patients.,Histopathologic material from 182 tumors in BRCA1 mutation carriers, 63 BRCA2 carriers, and 109 controls, collected as part of the international Breast Cancer Linkage Consortium were immunohistochemically stained for CK14, CK5/6, CK17, epidermal growth factor receptor (EGFR), and osteonectin.,All five basal markers were commoner in BRCA1 tumors than in control tumors (CK14: 61% versus 12%; CK5/6: 58% versus 7%; CK17: 53% versus 10%; osteonectin: 43% versus 19%; EGFR: 67% versus 21%; P < 0.0001 in each case). In a multivariate analysis, CK14, CK5/6, and estrogen receptor (ER) remained significant predictors of BRCA1 carrier status. In contrast, the frequency of basal markers in BRCA2 tumors did not differ significant from controls.,The use of cytokeratin staining in combination with ER and morphology provides a more accurate predictor of BRCA1 mutation status than previously available, that may be useful in selecting patients for BRCA1 mutation testing. The high percentage of BRCA1 cases positive for EGFR suggests that specific anti-tyrosine kinase therapy may be of potential benefit in these patients.

文献信息
期刊
Clinical cancer research : an official journal of the American Association for Cancer Research
期刊简称
Clin Cancer Res
发表日期
2005-11-07
收录日期
2005-07-21
更新日期
2015-11-19
语言
英语
国家/地区
United States
NLM ID
9502500
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