Niu Yuanyuan, Wang Huijuan, Zhang Guowei, Ma Jie, Wei Bing, Ma Zhiyong
Department of Respiratory Medicine, Department of Pathology, the Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou 450008, China.
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Zhonghua Jie He He Hu Xi Za Zhi. 2014 Dec;37(12):919-23.
Epidermal growth factor receptor (EGFR) mutation status plays an important role in individual treatment of non-small cell lung cancer.However clinical tissue samples for mutation detection are not always available in advanced NSCLC. Thus an alternative method of EGFR mutation detection is required in NSCLC treatment.Recent studies have associated thyroid transcription factor 1 (TTF-1) with EGFR mutations in lung cancer.In this study, we detected expression of TTF-1 and EGFR mutations in 102 patients with advanced NSCLC and investigated the possibility of TTF-1 as a potential indicator of EGFR status.
Serum and tissue samples were collected from 102 patients with advanced NSCLC including 28 cases of EGFR mutation in 19 exon, 23 cases of EGFR mutation in 21 exon and 51 cases of WT EGFR. Protein levels of TTF-1 in serum were quantified by enzyme-linked immunosorbent assay (ELISA).Levels of TTF-1 in tissues were detected by immunohistochemistry (IHC). SPSS 17 statistical software was used to analyze the data.
In the serum the expression of TTF-1 in EGFR 19 and 21 exon MT groups both was higher than that in the WT group(19MT vs 21MT vs WT: 0.092 vs 0.083 vs 0.045; F = 27.653, P < 0.01), and the result of the tissues was the same (19MT vs 21MT vs WT: 0.682 vs 0.644 vs 0.441; F = 47.665, P < 0.01), but no differences between two MT groups were observed (P > 0.05). The ELISA results and the IHC results were consistent (r = 0.87, P < 0.01). The expression of TTF-1 in serum showed a relationship with smoking history (χ² = 4.639, P < 0.05), but not with sex, age, TNM stage and metastasis (P > 0.05).
These results indicated that TTF-1 expression was upregulated in EGFR mutated NSCLC compared to EGFR WT NSCLC. The level of TTF-1 maybe used as a potential marker of EGFR mutation status.
表皮生长因子受体(EGFR)突变状态在非小细胞肺癌的个体化治疗中起着重要作用。然而,在晚期非小细胞肺癌中,并非总能获得用于突变检测的临床组织样本。因此,非小细胞肺癌治疗中需要一种EGFR突变检测的替代方法。最近的研究将甲状腺转录因子1(TTF-1)与肺癌中的EGFR突变联系起来。在本研究中,我们检测了102例晚期非小细胞肺癌患者的TTF-1表达和EGFR突变情况,并探讨了TTF-1作为EGFR状态潜在指标的可能性。
收集102例晚期非小细胞肺癌患者的血清和组织样本,其中包括19外显子EGFR突变28例、21外显子EGFR突变23例以及EGFR野生型(WT)51例。采用酶联免疫吸附测定(ELISA)定量血清中TTF-1的蛋白水平。通过免疫组织化学(IHC)检测组织中TTF-1的水平。使用SPSS 17统计软件分析数据。
血清中,EGFR 19和21外显子突变组的TTF-1表达均高于野生型组(19MT组 vs 21MT组 vs WT组:0.092 vs 0.083 vs 0.045;F = 27.653,P < 0.01),组织检测结果相同(19MT组 vs 21MT组 vs WT组:0.682 vs 0.644 vs 0.441;F = 47.665,P < 0.01),但两个突变组之间未观察到差异(P > 0.05)。ELISA结果与IHC结果一致(r = 0.87,P < 0.01)。血清中TTF-1的表达与吸烟史有关(χ² = 4.6 39,P < 0.05),但与性别、年龄、TNM分期和转移无关(P > 0.05)。
这些结果表明,与EGFR野生型非小细胞肺癌相比,EGFR突变的非小细胞肺癌中TTF-1表达上调。TTF-1水平可能用作EGFR突变状态的潜在标志物。