首页> 外文期刊>Journal of thoracic oncology: official publication of the International Association for the Study of Lung Cancer >Thymidylate synthase protein expression by IHC and gene copy number by SISH correlate and show great variability in non-small cell lung cancer
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Thymidylate synthase protein expression by IHC and gene copy number by SISH correlate and show great variability in non-small cell lung cancer

机译:非小细胞肺癌中IHC的胸苷酸合酶蛋白表达与SISH的基因拷贝数相关并显示出很大的变异性

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Introduction: Increased expression of thymidylate synthase (TS) is thought to be associated with resistance to TS-targeting drugs, e.g., pemetrexed. METHODS: TS protein expression (PE) and gene copy number (GCN) were assayed using immunohistochemistry and silver in situ hybridization, respectively, on primary tumors of 189 resected non-small cell lung patients. Associations with pathological and clinical features and prognosis were explored. RESULTS: Median immunohistochemistry H-score was 220 (range, 10-380) on a 0 to 400 scale; 17% of the patients had a TS expression of 300 or more. TS PE expression did not significantly differ by histology and did not significantly associate with disease-free survival (DFS) or overall survival (OS). However, there was a tendency for increased DFS (p = 0.12) and OS (p = 0.12) in PE positive (>median) squamous-cell carcinoma (SCC) patients. Median GCN was 2.5 genesucleus (range, 1.4-9.6); 29% of patients had GCN of 3 or more, 7% of 4 or more and 0.8% amplification. GCN differed by histology (p = 0.015); 50% of SCCs having GCN more than 2.5 versus 32% of adenocarcinomas. There was no significant relationship between TS GCN and DFS or OS; however, a trend toward better DFS (p = 0.18) and OS (p = 0.10) with increased GCN in SCCs was observed. TS GCN was significantly correlated with PE (r = 0.30, p = 0.0009). CONCLUSIONS: TS PE and GCN vary widely in non-small cell lung and correlate significantly with each other. TS GCN is higher in SCCs, whereas TS PE does not associate with histological subtypes, clinical features, or survival. Variability of TS PE and GCN may indicate potential benefit from pemetrexed therapy in selected SCC patients.
机译:简介:胸苷酸合酶(TS)的表达增加被认为与抗TS靶向药物(如培美曲塞)有关。方法:采用免疫组织化学和银原位杂交技术分别对189例切除的非小细胞肺癌患者的原发肿瘤进行TS蛋白表达(PE)和基因拷贝数(GCN)测定。探讨与病理,临床特征和预后的关系。结果:免疫组化H值中位数为0(至400),为220(范围:10-380); 17%的患者的TS表达为300或更高。 TS PE的表达在组织学上无显着差异,并且与无病生存期(DFS)或总生存期(OS)无关。然而,PE阳性(>中位)鳞状细胞癌(SCC)患者存在DFS(p = 0.12)和OS(p = 0.12)增加的趋势。 GCN中位数为2.5个基因/核(范围1.4-9.6); 29%的患者的GCN为3或更高,7%的GCN为4或更高,放大率为0.8%。 GCN的组织学差异(p = 0.015); 50%的GCC大于2.5的SCC与32%的腺癌相比。 TS GCN与DFS或OS之间没有显着关系;然而,观察到随着SCC中GCN的增加,DFS(p = 0.18)和OS(p = 0.10)趋于更好的趋势。 TS GCN与PE显着相关(r = 0.30,p = 0.0009)。结论:TS PE和GCN在非小细胞肺癌中差异很大,并且相互之间具有显着相关性。 TS GCN在SCC中较高,而TS PE与组织学亚型,临床特征或生存率无关。 TS PE和GCN的变异性可能表明培美曲塞治疗对部分SCC患者有潜在的益处。

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