Xia Weiya, Chen Jin-Shing, Zhou Xian, Sun Pei-Rong, Lee Dung-Fang, Liao Yong, Zhou Binhua P, Hung Mien-Chie
Departments of Molecular and Cellular Oncology, The University of Texas M D Anderson Cancer Center, Houston, Texas 77030, USA.
Clin Cancer Res. 2004 Jun 1;10(11):3815-24. doi: 10.1158/1078-0432.CCR-03-0527.
The diversity of biological functions makes p21(Cip1/WAF1) (p21) a controversial marker in predicting the prognosis of breast cancer patients. Recent laboratory studies revealed that the regulation of p21 function could be related to different subcellular localizations of p21 by Akt-induced phosphorylation at threonine 145 in HER2/neu-overexpressing breast cancer cells. The purpose of this study was to verify these findings in clinical settings.
The expression status of the key biological markers in the HER2/neu-Akt-p21 pathway in 130 breast cancer specimens was evaluated by immunohistochemical staining and correlated with patients' clinical parameters and survival. In addition, an antibody against phospho-p21 at threonine 145 [phospho-p21 (T145)] was also used for better validation of these findings.
Cytoplasmic localization of p21 is highly correlated with overexpression of phospho-p21 (T145). Both cytoplasmic p21 and overexpression of phospho-p21 (T145) are associated with high expression of HER2/neu and phospho-Akt. Cytoplasmic localization of p21 and overexpression of phospho-p21 (T145), HER2/neu, and phospho-Akt are all associated with worse overall survival. Multivariate analysis of the Cox proportional hazard regression model revealed that cytoplasmic p21 and overexpression of HER2/neu are independently associated with increased risk of death. Combining these two factors stratified patients' survival into four distinct groups, with a 5-year survival rate of 79% in low HER2/neu and negative/nuclear p21 patients, 60% in high HER2/neu and negative/nuclear p21 patients, 29% in low HER2/neu and cytoplasmic p21 patients, and 16% in high HER2/neu and cytoplasmic p21 patients.
The present study, in addition to supporting the mechanisms of p21 regulation derived from laboratory investigation, demonstrates the prognostic importance of phospho-p21 (T145) for the first time and also provides a novel combination of p21 and HER2/neu for better stratification of patients' survival than any single clinicopathological or biological marker that may play important diagnostic and therapeutic roles for breast cancer patients.
生物学功能的多样性使得p21(Cip1/WAF1)(p21)在预测乳腺癌患者预后方面成为一个有争议的标志物。最近的实验室研究表明,在HER2/neu过表达的乳腺癌细胞中,Akt诱导的苏氨酸145位点磷酸化可使p21功能的调节与p21不同的亚细胞定位相关。本研究的目的是在临床环境中验证这些发现。
通过免疫组织化学染色评估130例乳腺癌标本中HER2/neu-Akt-p21通路关键生物标志物的表达状态,并将其与患者的临床参数和生存率相关联。此外,还使用了一种针对苏氨酸145位点磷酸化p21 [磷酸化p21(T145)]的抗体,以更好地验证这些发现。
p21的细胞质定位与磷酸化p21(T145)的过表达高度相关。细胞质p21和磷酸化p21(T145)的过表达均与HER2/neu和磷酸化Akt的高表达相关。p21的细胞质定位、磷酸化p21(T145)、HER2/neu和磷酸化Akt的过表达均与较差的总生存期相关。Cox比例风险回归模型的多变量分析显示,细胞质p21和HER2/neu的过表达与死亡风险增加独立相关。将这两个因素结合起来可将患者的生存分为四个不同的组,HER2/neu低表达且p21为阴性/细胞核型的患者5年生存率为79%,HER2/neu高表达且p21为阴性/细胞核型的患者为60%,HER2/neu低表达且p21为细胞质型的患者为29%,HER2/neu高表达且p21为细胞质型的患者为16%。
本研究除了支持实验室研究所推导的p21调节机制外,首次证明了磷酸化p21(T145)的预后重要性,还提供了p21和HER2/neu的一种新组合,与任何单一的临床病理或生物标志物相比,能更好地对患者生存进行分层,这可能对乳腺癌患者具有重要的诊断和治疗作用。