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Negative reactions of BRAF BRAF mutation‐specific immunohistochemistry to non‐V600E non‐V600E mutations of BRAF BRAF

机译:漂亮漂亮的突变特异性免疫组化对非V600E非V600E突变的负面反应很好

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摘要

BRAF mutations are rare driver mutations in non‐small cell lung cancer (NSCLC), accounting for 1%–2% of the driver mutations, and the mutation spectrum has a wide range in contrast to other tumors. While V600E is a dominant mutation in melanoma, more than half of the mutations in NSCLCs are non‐V600E. However, treatment with dabrafenib plus trametinib targets the BRAF V600E mutation exclusively. Therefore, distinguishing between V600E and non‐V600E mutations is crucial for biomarker testing in NSCLC in order to determine treatment of choice. Immunohistochemistry (IHC) using the BRAF V600E mutation‐specific antibody is clinically used in melanoma patients, but little is known about its application in NSCLC, particularly with regard to the assay performance for non‐V600E mutations. In the present study, we examined 117 tumors with BRAF mutations, including 30 with non‐V600E mutations, using BRAF mutation‐specific IHC. None of the tumors with non‐V600E mutations, including two compound mutations, showed a positive reaction. Furthermore, all V600E mutations were positive except for one case with combined BRAF V600E and K601_W604 deletion. Our findings confirmed that the BRAF V600E mutation‐specific IHC is specific without any cross‐reactions to non‐V600E mutations, suggesting that this assay can be a useful screening tool in clinical practice.
机译:BRAF突变是非小细胞肺癌(NSCLC)中的稀有驾驶员突变,占驾驶员突变的1%-2%,突变谱与其他肿瘤形成宽范围。虽然V600E是黑色素瘤中的显性突变,但NSCLC中的超过一半突变是非V600E。然而,用Dabrafenib Plus Trametinib治疗专门针对BRAF V600E突变。因此,区分V600E和非V600E突变对于NSCLC中的生物标志物测试至关重要,以确定选择的治疗。免疫组织化学(IHC)使用BRAF V600E突变特异性抗体是在黑色素瘤患者中使用的临床上使用,但在NSCLC中的应用很少,特别是关于非V600E突变的测定性能。在本研究中,我们使用BRAF突变特异性IHC检查了BRAF突变的117例肿瘤,其中包括非V600E突变。没有非V600E突变的肿瘤,包括两种复合突变,显示出阳性反应。此外,除了组合BRAF V600E和K601_W604删除的一种情况外,所有V600E突变都是阳性的。我们的研究结果证实,BRAF V600E突变特异性IHC特异性没有对非V600E突变的任何交叉反应,表明该测定可以是临床实践中有用的筛选工具。

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