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Human Cancer Biology |
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)-
, 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-
(ER-
–), 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-
–, improved by combining them together (CCL5+/ER-
–: P = 0.0001), being highly evident in the stage IIA subgroup [CCL5+/ER-
– (P = 0.0003); ER-
– (P = 0.0315)]. In the stage II group as a whole, the combinations of CCL5–/ER-
+ and CCL5–/PR+ were highly correlated with an improved prognosis. Multivariate analysis indicated that, in stage II patients, ER-
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-
– combination providing improved prediction of disease progression, primarily in the stage IIA subgroup.
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