Chen Tai-Di, Chang Il-Chi, Liu Hui-Ping, Wu Yi-Cheng, Wang Chi-Liang, Chen Ya-Ting, Chen Yi-Rong, Huang Shiu-Feng
Department of Pathology, Chang Gung Memorial Hospital at Linkou, Chang Gung University College of Medicine, Taoyuan, Taiwan.
Chang Gung Med J. 2012 Jul-Aug;35(4):309-17. doi: 10.4103/2319-4170.106140.
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.
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.
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).
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.
最近在非小细胞肺癌(NSCLC)中发现了具有转化活性的棘皮动物微管相关蛋白样4-间变性淋巴瘤激酶(EML4-ALK)融合基因。此外,与没有该融合基因的NSCLC患者相比,携带EML4-ALK融合基因的患者在接受ALK抑制剂治疗后有显著反应且无进展生存期更长。然而,台湾NSCLC患者中EML4-ALK融合基因的发生率以及临床和分子特征仍不清楚。
从长庚纪念医院组织库获取64份新鲜冷冻肿瘤标本用于RNA提取和EML4-ALK融合基因检测。所有这些患者的肺肿瘤石蜡切片均可用,并通过免疫组织化学(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。
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了EML4-ALK融合基因。2例肿瘤为变体3(3a + 3b,以3b为主),通过IHC染色ALK呈强阳性(3+)。1例肿瘤为变体1,ALK呈中度阳性(2+)。ALK野生型肿瘤均无ALK强阳性染色。与其他临床和分子特征相比,仅ALK的IHC染色与EML4-ALK融合基因显著相关(p = 0.0002)。
通过IHC研究检测到的ALK过表达可能是一种有前景的EML4-ALK融合基因检测方法,值得用更多样本进一步证实。