三种针对非小细胞肺癌表皮生长因子及其受体的单克隆抗体的免疫组化特征:它们在选择免疫疗法患者中的潜在用途。

Journal of biomarkers Pub Date : 2013-01-01 Epub Date: 2012-12-11 DOI:10.1155/2013/627845
Charles E Rengifo, Rancés Blanco, Damián Blanco, Mercedes Cedeño, Milagros Frómeta, Enrique Rengifo Calzado
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引用次数: 0

摘要

我们需要适当的方法来确定哪些肺癌患者最有可能从针对表皮生长因子受体/表皮生长因子(EGFR/EGF)的靶向药物中获益。为此,我们评估了 ior egf/r3 单克隆抗体(Mab)在人类肺癌中的组织反应性及其在 NCI-H125 细胞中的生物活性。此外,我们还使用 CB-EGF1 和 CB-EGF2 这两种单克隆抗体评估了组织中 EGF 的表达。在33.33%的小细胞肺癌(SCLC)和62.71%的非小细胞肺癌(NSCLC)中分别检测到表皮生长因子受体的过表达。实验还证明了 ior egf/r3 Mab 与表皮生长因子受体胞外结构域结合的能力,它能抑制细胞增殖并诱导 NCI-H125 细胞凋亡。在约 17% 的 SCLC 和 70% 的 NSCLC 中分别观察到 EGF 表达。然而,CB-EGF1 和 CB-EGF2 的反应性存在差异。在 16.67% 的 SCLC 和 57.63% 的 NSCLC 患者中分别观察到表皮生长因子受体和表皮生长因子受体的双重表达。但是,只有在 NSCLC 中才发现了它们之间的相关性。我们的研究结果建议开发使用 ior egf/r3 和/或 CB-EGF1 Mabs 的诊断试剂盒,以便更好地选择接受表皮生长因子受体/表皮生长因子受体靶向治疗的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Immunohistochemical Characterization of Three Monoclonal Antibodies Raised against the Epidermal Growth Factor and Its Receptor in Non-Small-Cell Lung Cancer: Their Potential Use in the Selection of Patients for Immunotherapy.

Adequate methods to identify which lung cancer patients are most likely to benefit from the targeted drugs against both epidermal growth factor receptor/epidermal growth factor (EGFR/EGF) are needed. For this reason, we evaluated both the tissue reactivity of ior egf/r3 monoclonal antibody (Mab) in human lung carcinomas and its biological activity in NCI-H125 cells. Additionally, we assessed the tissue expression of EGF using two Mabs, CB-EGF1 and CB-EGF2. The overexpression of EGFR was detected in 33.33% and 62.71% of small-cell lung carcinoma (SCLC) and non-small-cell lung carcinoma (NSCLC), respectively. The ability of ior egf/r3 Mab to bind the extracellular domain of EGFR inhibiting cell proliferation and inducing apoptosis in NCI-H125 cells was also demonstrated. The EGF expression was observed in about 17% and 70% of SCLC and NSCLC, respectively. However, differences in the reactivity of CB-EGF1 and CB-EGF2 were evidenced. A dual expression of EGFR and EGF was observed in 16.67% and 57.63% of SCLC and NSCLC patients, respectively. But, a correlation between them was only obtained in NSCLC. Our results permit to recommend the development of diagnostic kits using ior egf/r3 and/or CB-EGF1 Mabs in order to achieve a better selection of patients to EGFR/EGF-targeting treatment.

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