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Detection of EGFR mutations with mutation-specific antibodies in stage IV non-small-cell lung cancer

机译:IV期非小细胞肺癌中突变特异性抗体检测EGFR突变

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Background Immunohistochemistry (IHC) with mutation-specific antibodies may be an ancillary method of detecting EGFR mutations in lung cancer patients. Methods EGFR mutation status was analyzed by DNA assays, and compared with IHC results in five non-small-cell lung cancer (NSCLC) cell lines and tumor samples from 78 stage IV NSCLC patients. Results IHC correctly identified del 19 in the H1650 and PC9 cell lines, L858R in H1975, and wild-type EGFR in H460 and A549, as well as wild-type EGFR in tumor samples from 22 patients. IHC with the mAb against EGFR with del 19 was highly positive for the protein in all 17 patients with a 15-bp (ELREA) deletion in exon 19, whereas in patients with other deletions, IHC was weakly positive in 3 cases and negative in 9 cases. IHC with the mAb against the L858R mutation showed high positivity for the protein in 25/27 (93%) patients with exon 21 EGFR mutations (all with L858R) but did not identify the L861Q mutation in the remaining two patients. Conclusions IHC with mutation-specific mAbs against EGFR is a promising method for detecting EGFR mutations in NSCLC patients. However these mAbs should be validated with additional studies to clarify their possible role in routine clinical practice for screening EGFR mutations in NSCLC patients.
机译:背景技术具有突变特异性抗体的免疫组织化学(IHC)可能是检测肺癌患者EGFR突变的辅助方法。方法对78例IV期NSCLC患者的5种非小细胞肺癌(NSCLC)细胞系和肿瘤样品中的EGFR突变状态进行DNA分析,并与IHC结果进行比较。结果IHC正确鉴定了H1650和PC9细胞系中的del 19,H1975中的L858R,H460和A549中的野生型EGFR,以及22例患者的肿瘤样本中的野生型EGFR。在外显子19的15 bp(ELREA)缺失的所有17例患者中,IHC与针对EGFR 19的mAb的蛋白高度阳性,而在其他缺失的患者中,IHC在3例中弱阳性,在9例中阴性案件。具有针对L858R突变的mAb的IHC在25/27(93%)具有外显子21 EGFR突变的患者(全部为L858R)中显示出对该蛋白的高阳性,但在其余两名患者中未鉴定出L861Q突变。结论具有针对EGFR的突变特异性mAb的IHC是检测NSCLC患者中EGFR突变的有前途的方法。但是,应通过其他研究对这些mAb进行验证,以阐明它们在筛查NSCLC患者中EGFR突变的常规临床实践中的可能作用。

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