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首页> 外文期刊>Assay and drug development technologies >Activity assay of epidermal growth factor receptor tyrosine kinase inhibitors in triple-negative breast cancer cells using peptide-conjugated magnetic beads
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Activity assay of epidermal growth factor receptor tyrosine kinase inhibitors in triple-negative breast cancer cells using peptide-conjugated magnetic beads

机译:表皮生长因子受体酪氨酸激酶抑制剂在三阴性乳腺癌细胞中的活性研究

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摘要

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.
机译:三阴性乳腺癌(TNBC)是一种高度侵袭性的乳腺癌亚型,治疗选择有限。表皮生长因子受体I(EGFR)已成为TNBC中有希望的靶标。在临床试验中,抑制EGFR激酶的小分子成功有限,可能部分归因于在患者肿瘤中鉴定EGFR信号不准确。鉴于EGFR表达与其激活程度之间不存在简单的相关性,一种简单而可靠的工具可以量化肿瘤样品中的EGFR激酶活性,在预测患者特异性EGFR靶向疗法中可能具有治疗价值。这项研究报告了一种测定方法的发展,该方法可以通过使用以受控方向共价拴在磁珠上的肽报道分子定量分析TNBC细胞裂解物中的EGFR激酶活性和抑制剂敏感性。磁珠的使用提供了快速的样品处理和容易的产品分离。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这种方法的潜力。格式化用于微孔板,这种基于磁珠的激酶测定法可以用作对小分子抑制剂进行直接高通量筛选的补充方法。

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