Buck Miriam B, Fritz Peter, Dippon Juergen, Zugmaier Gerhard, Knabbe Cornelius
Robert Bosch Hospital, Department of Clinical Chemistry, Stuttgart, Germany.
Clin Cancer Res. 2004 Jan 15;10(2):491-8. doi: 10.1158/1078-0432.ccr-0320-03.
The role of transforming growth factor beta (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.
Expression of TGF-beta receptor I (TbetaRI) and TGFbeta receptor II (TbetaRII) was retrospectively analyzed by immunohistochemistry in 246 breast cancer patients.
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.
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.
转化生长因子β(TGF-β)在乳腺癌中的作用尚不明确;它既能发挥肿瘤抑制作用,也能产生促进作用。TGF-β信号转导系统的激活受激素调节。本研究旨在进一步分析TGF-β受体在乳腺癌中的作用,并评估其作为预后标志物的意义。
通过免疫组织化学方法对246例乳腺癌患者的TGF-β受体I(TβRI)和TGF-β受体II(TβRII)表达进行回顾性分析。
TβRI的表达与肿瘤大小(P < 0.001)和淋巴结状态(P = 0.012)密切相关,但与总生存期的相关性较弱(P = 0.056)。相比之下,在单因素分析中,TβRII对总生存期具有预后价值(P = 0.0370)。在雌激素受体(ER)阴性患者中,TβRII表达与总生存期显著降低相关(P = 0.0083)。在多因素分析中,TβRII被证明是一个独立且高度显著的预后标志物,风险比为6.8。ER和TβRII同时缺失与较长的总生存期相关,与ER阳性患者相当。
这项探索性研究的结果表明,TβRII是ER阴性患者总生存期的一个独立、高度显著的预后指标。此外,我们的结果支持一种乳腺癌进展机制,即TGF-β的肿瘤抑制作用选择性丧失,而肿瘤促进方面保持完整。