Clinical Cancer Research AACR Conference on Cancer Prevention
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Yaal-Hahoshen, N.
Right arrow Articles by Ben-Baruch, A.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Yaal-Hahoshen, N.
Right arrow Articles by Ben-Baruch, A.
Clinical Cancer Research Vol. 12, 4474-4480, August 1, 2006
© 2006 American Association for Cancer Research


Human Cancer Biology

The Chemokine CCL5 as a Potential Prognostic Factor Predicting Disease Progression in Stage II Breast Cancer Patients

Neora Yaal-Hahoshen1, Sima Shina4, Leonor Leider-Trejo2, Itay Barnea4, Esther L. Shabtai3, Elina Azenshtein4, Iulia Greenberg1, Iafa Keydar4 and Adit Ben-Baruch4

Authors' Affiliations: Departments of 1 Oncology and 2 Pathology and 3 Statistical Service, Tel Aviv Sourasky Medical Center; 4 Department of Cell Research and Immunology, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel

Requests for reprints: Adit Ben-Baruch, Department of Cell Research and Immunology, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv 69978, Israel. Phone: 972-3-6407933; Fax: 972-3-6422046; E-mail: aditbb{at}tauex.tau.ac.il.

Purpose: The aim of this study was to determine the prognostic value of the chemokine CCL5, considered as a promalignancy factor in breast cancer, in predicting breast cancer progression and to evaluate its ability to strengthen the prognostic significance of other biomarkers.

Experimental Design: The expression of CCL5, alone and in conjunction with estrogen receptor (ER)-{alpha}, ER-ß, progesterone receptor (PR), and HER-2/neu (ErbB2), was determined in breast tumor cells by immunohistochemistry. The study included 142 breast cancer patients, including individuals in whom disease has progressed.

Results: Using Cox proportional hazard models, univariate analysis suggested that, in stage I breast cancer patients, CCL5 was not a significant predictor of disease progression. In contrast, in stage II patients, the expression of CCL5 (CCL5+), the absence of ER-{alpha} (ER-{alpha}), and the lack of PR expression (PR) increased significantly the risk for disease progression (P = 0.0045, 0.0041, and 0.0107, respectively). The prognostic strength of CCL5, as well as of ER-{alpha}, improved by combining them together (CCL5+/ER-{alpha}: P = 0.0001), being highly evident in the stage IIA subgroup [CCL5+/ER-{alpha} (P = 0.0003); ER-{alpha} (P = 0.0315)]. In the stage II group as a whole, the combinations of CCL5/ER-{alpha}+ and CCL5/PR+ were highly correlated with an improved prognosis. Multivariate analysis indicated that, in stage II patients, ER-{alpha} and CCL5 were independent predictors of disease progression.

Conclusions: CCL5 could be considered as a biomarker for disease progression in stage II breast cancer patients, with the CCL5+/ER-{alpha} combination providing improved prediction of disease progression, primarily in the stage IIA subgroup.




This article has been cited by other articles:


Home page
Clin. Cancer Res.Home page
G. Sauer, N. Schneiderhan-Marra, C. Kazmaier, K. Hutzel, K. Koretz, R. Muche, R. Kreienberg, T. Joos, and H. Deissler
Prediction of Nodal Involvement in Breast Cancer Based on Multiparametric Protein Analyses from Preoperative Core Needle Biopsies of the Primary Lesion
Clin. Cancer Res., June 1, 2008; 14(11): 3345 - 3353.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 2006 by the American Association for Cancer Research.