Short Sarah M, Yoder Brian J, Tarr Shannon M, Prescott Nichole L, Laniauskas Simas, Coleman Kara A, Downs-Kelly Erinn, Pettay James D, Choueiri Toni K, Crowe Joseph P, Tubbs Raymond R, Budd Thomas G, Hicks David G
Department of Anatomic and Clinical Pathology L25, Cleveland, Ohio, USA.
Breast J. 2007 Mar-Apr;13(2):130-9. doi: 10.1111/j.1524-4741.2007.00389.x.
Paxillin, a cytoskeletal focal adhesion adaptor protein, has been shown to be transcriptionally up-regulated and phosphorylated by human epidermal growth factor receptor-2 (HER2) signaling in vitro. Paxillin expression may also correlate with HER2 amplification in breast cancer patients. In the current study, we sought to explore the relationship further between paxillin expression and clinicopathologic features and clinical outcome in breast cancer. A total of 314 primary invasive breast carcinomas were assessed for paxillin expression via immunohistochemistry. Paxillin immunoreactivity was compared with estrogen receptor/progesterone receptor status, HER2 status by silver in situ hybridization, age, tumor size, stage, Bloom-Richardson grade, nodal status, disease-free survival (DFS), and overall survival (OS). Paxillin expression was identified in 27.7% of breast carcinomas as diffuse cytoplasmic staining and the expression correlated with HER2 overexpression (p < 0.001). The influence of paxillin on clinical outcome, in particular the response to chemotherapy, appeared to differ depending on the HER2 status of the tumor. For the subset of HER2 nonamplified cases treated with chemotherapy, patients whose tumor showed a loss of paxillin expression demonstrated a significantly lengthened DFS and OS. In contrast, loss of paxillin expression in the HER2 amplified subset of patients who received chemotherapy correlated with a significantly worse outcome. These data suggest that paxillin up-regulation may be a part of the HER2 pathway in some breast cancers and, furthermore, paxillin expression may also influence the clinical response to chemotherapy, depending upon the HER2 status of a given patient's tumor. Further study of a role for paxillin expression in predicting response to cytotoxic regimens or targeted treatments is warranted.
桩蛋白是一种细胞骨架粘着斑衔接蛋白,在体外已被证明可被人表皮生长因子受体2(HER2)信号传导转录上调并磷酸化。桩蛋白的表达也可能与乳腺癌患者的HER2扩增相关。在本研究中,我们试图进一步探讨桩蛋白表达与乳腺癌临床病理特征及临床结局之间的关系。通过免疫组织化学对总共314例原发性浸润性乳腺癌进行桩蛋白表达评估。将桩蛋白免疫反应性与雌激素受体/孕激素受体状态、通过银原位杂交检测的HER2状态、年龄、肿瘤大小、分期、布鲁姆-理查森分级、淋巴结状态、无病生存期(DFS)和总生存期(OS)进行比较。在27.7%的乳腺癌中发现桩蛋白表达为弥漫性细胞质染色,且该表达与HER2过表达相关(p<0.001)。桩蛋白对临床结局的影响,尤其是对化疗的反应,似乎因肿瘤的HER2状态而异。对于接受化疗的HER2非扩增病例子集,肿瘤显示桩蛋白表达缺失的患者DFS和OS显著延长。相反,接受化疗的HER2扩增患者子集中桩蛋白表达缺失与显著更差的结局相关。这些数据表明,桩蛋白上调可能是某些乳腺癌中HER2通路的一部分,此外,桩蛋白表达也可能影响对化疗的临床反应,这取决于特定患者肿瘤的HER2状态。有必要进一步研究桩蛋白表达在预测对细胞毒性方案或靶向治疗反应中的作用。