Academic Oncology, University of Nottingham, School of Molecular Medical Sciences, Nottingham University Hospitals NHS Trust, City Hospital Campus, Nottingham NG5 1PB, UK.
Breast. 2011 Oct;20(5):413-8. doi: 10.1016/j.breast.2011.04.002. Epub 2011 May 4.
Metastasis of breast cancer is a major contributor to mortality. Histological assessment of vascular invasion (VI) provides important prognostic information and demonstrates that VI occurs predominantly via lymphatics in breast cancer. We sought to examine genes and proteins involved in lymphovascular invasion (LVI) to understand the mechanisms of this key disease process. A gene expression array of 91 breast cancer patients was analysed by an Artificial Neural Network (ANN) approach using LVI to supervise the analysis. 89 transcripts were significantly associated (p<0.001) with the presence of LVI. Calpastatin, a specific calpain inhibitor, had the second lowest selection error and was investigated in breast cancer specimens using real-time PCR (n=56) and immunohistochemistry (n=53). Both calpastatin mRNA and protein levels were significantly associated with the presence of LVI (p=0.014 and p=0.025 respectively). The data supports the hypothesis that calpastatin may play a role in regulating the initial metastatic dissemination of breast cancer.
乳腺癌转移是导致死亡率的主要原因之一。血管侵犯(VI)的组织学评估提供了重要的预后信息,并表明 VI 主要通过乳腺癌中的淋巴管发生。我们试图研究参与淋巴管侵犯(LVI)的基因和蛋白,以了解这一关键疾病过程的机制。使用 LVI 对 91 例乳腺癌患者的基因表达数组进行了人工神经网络(ANN)分析。有 89 个转录本与 LVI 的存在显著相关(p<0.001)。钙蛋白酶抑制剂钙蛋白酶抑制剂(Calpastatin)的选择错误最低,在 56 例乳腺癌标本中使用实时 PCR(n=56)和免疫组织化学(n=53)进行了研究。钙蛋白酶抑制剂 mRNA 和蛋白水平均与 LVI 的存在显著相关(p=0.014 和 p=0.025)。该数据支持钙蛋白酶抑制剂可能在调节乳腺癌初始转移扩散中发挥作用的假设。