免疫组化研究非小细胞肺癌间变性淋巴瘤激酶过表达与EML4-ALK融合基因的相关性

Tai-Di Chen, Il-Chi Chang, Hui-Ping Liu, Yi-Cheng Wu, Chi-Liang Wang, Ya-Ting Chen, Yi-Rong Chen, Shiu-Feng Huang
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引用次数: 8

摘要

背景:最近在非小细胞肺癌(NSCLC)中发现了具有转化活性的棘皮微管相关蛋白样4-间变性淋巴瘤激酶(EML4-ALK)融合基因。此外,具有EML4-ALK融合基因的NSCLC患者在ALK抑制剂治疗后具有显着的反应和更长的无进展生存期。然而,EML4-ALK融合基因在台湾NSCLC患者中的发病率、临床及分子特征尚不清楚。方法:从长庚纪念医院组织库中获取64例新鲜冷冻肿瘤标本,进行RNA提取和EML4-ALK融合基因检测。所有患者均获得肺肿瘤石蜡切片,并通过免疫组化(IHC)研究分析ALK蛋白表达。结果与临床和分子生物标志物相关。结果:64例肿瘤中有3例(4.7%)存在EML4-ALK融合基因。2例为腺癌,1例为腺鳞癌。20例非鳞状细胞癌患者存在表皮生长因子受体(EGFR)突变,因此在14.3%的EGFR野生型非鳞状细胞癌中发现EML4-ALK融合基因。两个肿瘤为变体3 (3a+3b,以3b为主),IHC染色显示ALK强染色(3+)。一个肿瘤为变异1,ALK呈中等(2+)染色。ALK野生型肿瘤均无强ALK染色。与其他临床和分子特征相比,只有ALK的IHC染色与EML4-ALK融合基因显著相关(p = 0.0002)。结论:免疫组化研究检测ALK过表达是一种很有前途的检测EML4-ALK融合基因的方法,值得更多样本进一步证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Correlation of anaplastic lymphoma kinase overexpression and the EML4-ALK fusion gene in non-small cell lung cancer by immunohistochemical study.

Background: Recently the echinoderm microtubule-associated protein-like 4-anaplastic lymphoma kinase (EML4-ALK) fusion gene with transforming activity was identified in non-small cell lung cancer (NSCLC). In addition, NSCLC patients with the EML4-ALK fusion gene had a dramatic response and longer progression free survival after ALK inhibitor treatment than those without this fusion gene. However, the incidence and clinical and molecular characteristics of the EML4-ALK fusion gene in NSCLC patients of Taiwan are still unclear.

Methods: Sixty-four fresh frozen tumor specimens were obtained from the tissue bank of Chang Gung Memorial Hospital for RNA extraction and EML4-ALK fusion gene detection. Paraffin sections of lung tumors from all of these patients were available and were analyzed for ALK protein expression by immunohistochemical (IHC) study. The results were correlated with clinical and molecular biomarkers.

Results: Three of the 64 tumors (4.7%) had the EML4-ALK fusion gene. Two were adenocarcinomas, and one was adenosquamous carcinoma. Twenty patients with non-squamous cell carcinomas had epidermal growth factor receptor (EGFR) mutations, so the EML4-ALK fusion gene was found in 14.3% of EGFR wild type non-squamous cell carcinomas. Two tumors were variant 3 (3a+3b with 3b predominant) and had strong staining (3+) for ALK by IHC stains. One tumor was variant 1 and had moderate staining (2+) for ALK. None of the ALK wild type tumors had strong staining for ALK. When compared with other clinical and molecular features, only the IHC stain for ALK was significantly correlated with the EML4-ALK fusion gene (p = 0.0002).

Conclusions: ALK overexpression detected by IHC study could be a promising detection method for the EML4-ALK fusion gene and is worth further confirmation with more samples.

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