Home LiteratureArticle Details
PMID: 11774277 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Y-box factor YB-1 predicts drug resistance and patient outcome in breast cancer independent of clinically relevant tumor biologic factors HER2, uPA and PAI-1.

International journal of cancer ·Vol. 97 ·No. 3 ·2002-01-20 ·Pages 278-82

Janz M, Harbeck N, Dettmar P, Berger U, Schmidt A, Jürchott K, Schmitt M, Royer HD

Abstract

Intrinsic or acquired resistance to chemotherapy is responsible for failure of current treatment regimens in breast cancer patients. The Y-box protein YB-1 regulates expression of the P-glycoprotein gene mdr1, which plays a major role in the development of a multidrug-resistant tumor phenotype. In human breast cancer, overexpression and nuclear localization of YB-1 is associated with upregulation of P-glycoprotein. In our pilot study, we analyzed the clinical relevance of YB-1 expression in breast cancer (n = 83) after a median follow-up of 61 months and compared it with tumor-biologic factors already used for clinical risk-group discrimination, i.e., HER2, urokinase-type plasminogen activator (uPA) and plasminogen activator inhibitor type 1 (PAI-1). High YB-1 expression in tumor tissue and surrounding benign breast epithelial cells was significantly associated with poor patient outcome. In patients who received postoperative chemotherapy, the 5-year relapse rate was 66% in patients with high YB-1 expression. In contrast, in patients with low YB-1 expressions, no relapse has been observed so far. YB-1 expression thus indicates clinical drug resistance in breast cancer. Moreover, YB-1 correlates with breast cancer aggressiveness: in patients not treated with postoperative chemotherapy, those with low YB-1 expression are still free of disease, whereas the 5-year relapse rate in those with high YB-1 was 30%. There was no significant correlation between YB-1 expression and either HER2 expression or uPA and PAI-1 levels. Risk-group assessment achieved by YB-1 differed significantly from that by HER2 or uPA/PAI-1. In conclusion, YB-1 demonstrated prognostic and predictive significance in breast cancer by identifying high-risk patients in both the presence and absence of postoperative chemotherapy, independent of tumor-biologic factors currently available for clinical decision making.

MeSH Terms
Adult Aged Aged, 80 and over Breast/metabolism Breast Neoplasms/drug therapy,metabolism,surgery CCAAT-Enhancer-Binding Proteins/metabolism,physiology Cell Division DNA-Binding Proteins Disease-Free Survival Drug Resistance, Multiple Drug Resistance, Neoplasm Female Humans Immunohistochemistry Menopause Middle Aged NFI Transcription Factors Neoplasm Metastasis Nuclear Proteins Phenotype Plasminogen Activator Inhibitor 1/metabolism Postmenopause Premenopause Receptor, ErbB-2/metabolism Time Factors Transcription Factors Urokinase-Type Plasminogen Activator/metabolism Y-Box-Binding Protein 1
Chemicals
CCAAT-Enhancer-Binding Proteins DNA-Binding Proteins NFI Transcription Factors Nuclear Proteins Plasminogen Activator Inhibitor 1 Transcription Factors Y-Box-Binding Protein 1 YBX1 protein, human Receptor, ErbB-2 Urokinase-Type Plasminogen Activator
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Janz Martin
Department of Cell Growth and Differentiation, Max Delbrück Center for Molecular Medicine, Berlin, Germany.
Harbeck Nadia
Dettmar Peer
Berger Ursula
Schmidt Anja
Jürchott Karsten
Schmitt Manfred
Royer Hans-Dieter
Article Info
Journal
International journal of cancer
Abbr.
Int J Cancer
ISSN
0020-7136
Published
2002-01-20
Pages
278-82
Language
English
Region
United States
NLM ID
0042124
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]