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人肺癌中 FGFR1 的表达和基因拷贝数。

FGFR1 expression and gene copy numbers in human lung cancer.

机构信息

Institute of Pathology, Jena University Hospital, Friedrich-Schiller-University, Ziegelmuehlenweg 1, 07740 Jena, Germany.

出版信息

Virchows Arch. 2012 Jul;461(1):49-57. doi: 10.1007/s00428-012-1250-y. Epub 2012 May 31.

DOI:10.1007/s00428-012-1250-y
PMID:22648708
Abstract

FGFR1 is a receptor tyrosine kinase of which the ligands belong to the fibroblast growth factor family. To evaluate the significance of FGFR1 in lung cancer, we analysed tumours by immunohistochemistry (IHC) and fluorescence in situ hybridization (FISH). Tissue microarrays were constructed containing 380 lung cancer samples including squamous cell carcinomas (SCC), adenocarcinomas (ADC), non-small cell lung cancer not otherwise specified, metastases, neuroendocrine tumours, large cell lung cancer and small cell lung cancer. FGFR1 expression was analysed by IHC and scored semi-quantitatively by a four-tier approach (0, 1, 2, 3). Using dual-colour interphase FISH with probes specific for the locus on 8p12 and the centromere of chromosome 8 (CEN8), copy numbers of FGFR1 were determined. High expression of FGFR1 was associated with increased FGFR1 gene copy numbers in squamous cell carcinoma (p < 0.001). The FGFR1 locus was equally affected by copy number losses and gains. The higher FGFR1 gene copy numbers in SCC compared to ADC did not reach statistical significance. High copy number amplification of FGFR1 was a very rare event, the FGFR1/CEN8 signal ratio reaching a maximum value of 2.75. There were no significant associations between FGFR1 and clinicopathological parameters. Fibroblast growth factor signalling represents an interesting therapeutic target in lung cancer. However, the pathways are complex with potential oncogenic and anti-oncogenic activities. Our data may help to define criteria for selecting patients that may benefit from these new therapeutic options.

摘要

FGFR1 是一种受体酪氨酸激酶,其配体属于成纤维细胞生长因子家族。为了评估 FGFR1 在肺癌中的意义,我们通过免疫组织化学(IHC)和荧光原位杂交(FISH)分析了肿瘤。构建了包含 380 例肺癌样本的组织微阵列,包括鳞状细胞癌(SCC)、腺癌(ADC)、非小细胞肺癌未另作说明、转移瘤、神经内分泌肿瘤、大细胞肺癌和小细胞肺癌。通过 IHC 分析 FGFR1 表达,并采用四分级方法(0、1、2、3)进行半定量评分。使用针对 8p12 基因座和 8 号染色体着丝粒(CEN8)的探针进行双色间期 FISH,确定 FGFR1 的拷贝数。FGFR1 的高表达与鳞状细胞癌中 FGFR1 基因拷贝数的增加相关(p<0.001)。FGFR1 基因座同样受到拷贝数缺失和增益的影响。与 ADC 相比,SCC 中 FGFR1 基因的高拷贝数扩增虽未达到统计学意义。FGFR1 高拷贝数扩增是一种非常罕见的事件,FGFR1/CEN8 信号比值达到最大值 2.75。FGFR1 与临床病理参数之间没有显著关联。成纤维细胞生长因子信号代表了肺癌中一个有趣的治疗靶点。然而,这些途径非常复杂,具有潜在的致癌和抗致癌活性。我们的数据可能有助于定义选择可能受益于这些新治疗选择的患者的标准。

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Cancer Discov. 2011 Jun;1(1):78-89. doi: 10.1158/2159-8274.CD-11-0005.
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Personalized therapy of lung cancer.肺癌的个性化治疗。
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Increased FGFR1 copy number in lung squamous cell carcinomas.肺鳞状细胞癌中 FGFR1 拷贝数增加。
一项针对中国癌症患者成纤维细胞生长因子受体畸变的全面泛癌研究。
Ann Transl Med. 2020 Oct;8(20):1290. doi: 10.21037/atm-20-5118.
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mRNA Expression of FGFR1 as Potential Marker for Predicting Prognosis of Surgical Resection of Small Cell Lung Cancer may be better than Protein Expression and Gene Amplification.FGFR1的mRNA表达作为预测小细胞肺癌手术切除预后的潜在标志物可能优于蛋白表达和基因扩增。
J Cancer. 2020 May 22;11(16):4691-4699. doi: 10.7150/jca.44476. eCollection 2020.
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