Ghosh Gargi, Yan Xiaoliang, Kron Stephen J, Palecek Sean P
Department of Chemical and Biological Engineering, University of Wisconsin, Madison, 53706, USA.
Assay Drug Dev Technol. 2013 Feb;11(1):44-51. doi: 10.1089/adt.2012.454. Epub 2012 Sep 20.
Triple-negative breast cancer (TNBC) is a highly aggressive subtype of breast cancer with limited treatment options. Epidermal growth factor receptor I (EGFR) has emerged as a promising target in TNBC. Limited success of the EGFR kinase inhibiting small molecules in clinical trials may be attributed in part to inaccuracy in identifying EGFR signatures in patient tumors. In light of the absence of a simple correlation between EGFR expression and its degree of activation, a simple and reliable tool that can quantify EGFR kinase activity in tumor samples may be of therapeutic value in predicting patient-specific EGFR targeted therapies. This study reports the development of an assay that can quantitatively profile EGFR kinase activities and inhibitor sensitivities in TNBC cell lysates by using peptide reporters covalently tethered to magnetic beads in a controlled orientation. The use of magnetic beads provides rapid sample handling and easy product isolation. The potential of this approach was demonstrated by screening a set of five clinically relevant EGFR tyrosine kinase inhibitors. Formatted for microwell plates, this magnetic bead-based kinase assay may be used as a complementary approach for direct high-throughput screening of small molecule inhibitors.
三阴性乳腺癌(TNBC)是一种侵袭性很强的乳腺癌亚型,治疗选择有限。表皮生长因子受体I(EGFR)已成为TNBC中有前景的靶点。EGFR激酶抑制小分子在临床试验中的成效有限,部分原因可能是在患者肿瘤中识别EGFR特征不准确。鉴于EGFR表达与其激活程度之间缺乏简单的相关性,一种能够量化肿瘤样本中EGFR激酶活性的简单可靠工具,对于预测患者特异性EGFR靶向治疗可能具有治疗价值。本研究报告了一种检测方法的开发,该方法可通过使用以可控方向共价连接到磁珠上的肽报告分子,对TNBC细胞裂解物中的EGFR激酶活性和抑制剂敏感性进行定量分析。磁珠的使用提供了快速的样品处理和简便的产物分离。通过筛选一组五种临床相关的EGFR酪氨酸激酶抑制剂,证明了该方法的潜力。这种基于磁珠的激酶检测方法经过微孔板格式化后,可作为直接高通量筛选小分子抑制剂的补充方法。