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成纤维细胞生长因子受体 1 基因扩增和蛋白表达在人肺癌中的研究。

Fibroblast growth factor receptor 1 gene amplification and protein expression in human lung cancer.

机构信息

Institute of Pathology, University Medical Center, Göttingen, Germany.

Department of Thoracic and Cardiovascular Surgery, University Medical Center, Göttingen, Germany.

出版信息

Cancer Med. 2020 May;9(10):3574-3583. doi: 10.1002/cam4.2994. Epub 2020 Mar 24.

Abstract

BACKGROUND

Targeting fibroblast growth factor receptor 1 (FGFR1) is a potential treatment for squamous cell lung cancer (SQCLC). So far, treatment decision in clinical studies is based on gene amplification. However, only a minority of patients have shown durable response. Furthermore, former studies have revealed contrasting results regarding the impact of FGFR1 amplification and expression on patient's prognosis.

AIMS

Here, we analyzed prevalence and correlation of FGFR1 gene amplification and protein expression in human lung cancer and their impact on overall survival. MATERIALS & METHODS: FGFR1 gene amplification and protein expression were analyzed by fluorescence in situ hybridization and immunohistochemistry (IHC) in 208 SQCLC and 45 small cell lung cancers (SCLC). Furthermore, FGFR1 protein expression was analyzed in 121 pulmonary adenocarcinomas (ACs). Amplification and expression were correlated to each other, clinicopathological characteristics, and overall survival.

RESULTS

FGFR1 was amplified in 23% of SQCLC and 8% of SCLC. Amplification was correlated to males (P = .027) but not to overall survival. Specificity of immunostaining was verified by cellular CRISPR/Cas9 FGFR1 knockout. FGFR1 was strongly expressed in 9% of SQCLC, 35% of AC, and 4% of SCLC. Expression was correlated to females (P = .0187) and to the absence of lymph node metastasis in SQCLC (P = .018) with no significant correlation to overall survival. Interestingly, no significant correlation between amplification and expression was detected.

DISCUSSION

FGFR1 gene amplification does not seem to correlate to protein expression.

CONCLUSION

We believe that patient selection for FGFR1 inhibitors in clinical studies should be reconsidered. Neither FGFR1 amplification nor expression influences patient's prognosis.

摘要

背景

靶向成纤维细胞生长因子受体 1(FGFR1)是治疗鳞状细胞肺癌(SQCLC)的一种潜在方法。到目前为止,临床研究中的治疗决策是基于基因扩增。然而,只有少数患者表现出持久的反应。此外,以前的研究表明,FGFR1 扩增和表达对患者预后的影响存在矛盾的结果。

目的

本研究旨在分析 FGFR1 基因扩增和蛋白表达在人类肺癌中的流行率和相关性及其对总生存期的影响。

材料与方法

采用荧光原位杂交和免疫组织化学(IHC)分析 208 例 SQCLC 和 45 例小细胞肺癌(SCLC)中 FGFR1 基因扩增和蛋白表达。此外,还分析了 121 例肺腺癌(AC)中的 FGFR1 蛋白表达。将扩增和表达与彼此、临床病理特征和总生存期相关联。

结果

23%的 SQCLC 和 8%的 SCLC 存在 FGFR1 扩增。扩增与男性相关(P=0.027),但与总生存期无关。免疫染色的特异性通过细胞 CRISPR/Cas9 FGFR1 基因敲除得到验证。9%的 SQCLC、35%的 AC 和 4%的 SCLC 中 FGFR1 表达较强。表达与女性(P=0.0187)和 SQCLC 中无淋巴结转移相关(P=0.018),与总生存期无显著相关性。有趣的是,扩增和表达之间没有显著相关性。

讨论

FGFR1 基因扩增似乎与蛋白表达无关。

结论

我们认为,在临床研究中,FGFR1 抑制剂的患者选择应重新考虑。FGFR1 扩增和表达均不影响患者的预后。

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