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Prognostic significance of transforming growth factor β receptor II in estrogen receptor-negative breast cancer patients
被引:82
作者:
Buck, MB
Fritz, P
Dippon, J
Zugmaier, G
Knabbe, C
机构:
[1] Robert Bosch Krankenhaus, Dept Clin Chem, D-70376 Stuttgart, Germany
[2] Dr Margarete Fischer Bosch Inst Clin Pharmacol, D-7000 Stuttgart, Germany
[3] Univ Stuttgart, Dept Math, D-7000 Stuttgart, Germany
[4] Univ Marburg, Med Ctr, Dept Hematol & Oncol, Marburg, Germany
关键词:
D O I:
10.1158/1078-0432.CCR-0320-03
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Purpose: The role of transforming growth factor P (TGF-beta) in breast cancer is ambiguous; it can display both tumor suppressing and enhancing effects. Activation of the TGF-beta signal transduction system is subject to hormonal regulation. This study was conducted to further analyze the role of TGF-beta receptors in breast cancer and to evaluate their significance as prognostic markers. Experimental Design: Expression of TGF-beta receptor I (TbetaRI) and TGFbeta receptor II (TbetaRII) was retrospectively analyzed by immumohistochemistry in 246 breast cancer patients. Results: Expression of TbetaRI was strongly correlated with tumor size (P < 0.001) and nodal status (P = 0.012) but only weakly with overall survival (P = 0.056). In contrast, TbetaRII was prognostic for overall survival in univariate analysis (P = 0.0370). In estrogen receptor (ER) -negative patients TbetaRII expression was correlated with highly reduced overall survival (P = 0.0083). In multivariate analysis TbetaRII proved to be an independent and highly significant prognostic marker with a hazard ratio of 6.8. Simultaneous loss of both ER and TbetaRII was associated with longer overall survival times comparable with those of ER-positive patients. Conclusions: The results of this exploratory study show that TbetaRII is an independent, highly significant prognostic indicator for overall survival in ER-negative patients. In addition our results are supportive of a mechanism of breast cancer progression in which a selective loss of the tumor inhibitory action of TGFbeta takes place, whereas tumor-promoting aspects remain intact.
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页码:491 / 498
页数:8
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