PMID- 17541441 OWN - NLM STAT- MEDLINE DCOM- 20070921 LR - 20230210 IS - 0893-3952 (Print) IS - 0893-3952 (Linking) VI - 20 IP - 8 DP - 2007 Aug TI - Predominance of the basal type and HER-2/neu type in brain metastasis from breast cancer. PG - 864-70 AB - Although breast cancer is the second most common cause of central nervous system (CNS) metastases with a notable increase of incidence, only few studies on brain-metastasizing breast cancer are available. In this immunohistochemical and fluorescence in situ hybridization (FISH) study, metastases to the CNS (n=85) and primary breast cancers, with known involvement of the CNS (n=44) including paired primary and metastasized tumours (n=23), were investigated retrospectively for the expression of oestrogen- (ER) and progesterone- (PR) hormone receptors, Her-2/neu, epidermal growth factor receptor (EGFR), Ki-67, and cytokeratins (CKs) 5/14. The majority of brain metastases were steroid hormone receptor negative (ER 66%, PR 82%) corresponding to the findings in primary tumours with known involvement of the CNS (68% ER-negative, 75% PR-negative). The frequency of HER-2/neu-overexpressing or -amplified cancers was increased in both groups (34 and 32%, respectively). EGFR expression was more frequent in metastases (41%) than in primary tumours (16%). The proportions of cases with a basal phenotype were 26 and 30%, respectively. In paired primary tumours and metastases to the CNS, constancy of Her-2/neu status was observed in 87% of cases with only one sample turning Her-2/neu-negative and two samples acquiring overexpression/amplification in brain metastases. In contrast, steroid hormone receptors exhibited more frequently a loss of expression (17%) than a gain (9%) with 74% revealing a constant phenotype. We conclude that brain-metastasizing breast cancer belongs predominantly to the basal type or Her-2/neu type. Primary and metastatic tumours differ from each other only in a minority of cases, leading rather to a loss of steroid hormone receptors and to a gain of EGFR and Her-2/neu. FAU - Gaedcke, Jochen AU - Gaedcke J AD - Institute of Pathology, Medizinische Hochschule Hannover, Hannover, Germany. FAU - Traub, Frank AU - Traub F FAU - Milde, Simone AU - Milde S FAU - Wilkens, Ludwig AU - Wilkens L FAU - Stan, Alexandru AU - Stan A FAU - Ostertag, Helmut AU - Ostertag H FAU - Christgen, Mathias AU - Christgen M FAU - von Wasielewski, Reinhard AU - von Wasielewski R FAU - Kreipe, Hans H AU - Kreipe HH LA - eng PT - Comparative Study PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20070601 PL - United States TA - Mod Pathol JT - Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc JID - 8806605 RN - 0 (KRT14 protein, human) RN - 0 (KRT5 protein, human) RN - 0 (Keratin-14) RN - 0 (Keratin-5) RN - 0 (Ki-67 Antigen) RN - 0 (Receptors, Estrogen) RN - 0 (Receptors, Progesterone) RN - EC 2.7.10.1 (ERBB2 protein, human) RN - EC 2.7.10.1 (ErbB Receptors) RN - EC 2.7.10.1 (Receptor, ErbB-2) SB - IM MH - Brain Neoplasms/*chemistry/genetics/secondary MH - Breast Neoplasms/*chemistry/genetics/pathology MH - Cell Proliferation MH - ErbB Receptors/analysis MH - Female MH - Gene Expression Regulation, Neoplastic MH - Humans MH - Immunohistochemistry/methods MH - In Situ Hybridization, Fluorescence MH - Keratin-14/analysis MH - Keratin-5/analysis MH - Ki-67 Antigen/analysis MH - Neoplasms, Basal Cell/*chemistry/genetics/secondary MH - Receptor, ErbB-2/*analysis/genetics MH - Receptors, Estrogen/analysis MH - Receptors, Progesterone/analysis MH - Retrospective Studies MH - Tissue Array Analysis EDAT- 2007/06/02 09:00 MHDA- 2007/09/22 09:00 CRDT- 2007/06/02 09:00 PHST- 2007/06/02 09:00 [pubmed] PHST- 2007/09/22 09:00 [medline] PHST- 2007/06/02 09:00 [entrez] AID - S0893-3952(22)03282-3 [pii] AID - 10.1038/modpathol.3800830 [doi] PST - ppublish SO - Mod Pathol. 2007 Aug;20(8):864-70. doi: 10.1038/modpathol.3800830. Epub 2007 Jun 1.