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首页> 外文期刊>Clinical cancer research: an official journal of the American Association for Cancer Research >Genetic and expression analysis of HER-2 and EGFR genes in salivary duct carcinoma: Empirical and therapeutic significance
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Genetic and expression analysis of HER-2 and EGFR genes in salivary duct carcinoma: Empirical and therapeutic significance

机译:唾液管癌中HER-2和EGFR基因的遗传和表达分析:经验和治疗意义

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Purpose: Salivary duct carcinoma overexpresses epidermal growth factor receptor (EGFR) and HER-2, although the underlying mechanisms remain undefined. Because of the potential utilization of these markers as treatment targets, we evaluated protein and gene status by several techniques to determine complementary value. Experimental Design: A tissue microarray of 66 salivary duct carcinomas was used for immunohistochemical analysis of HER-2 and EGFR expression (semiquantitatively evaluated into a three-tiered system), and fluorescence in situ hybridization for gene copy number, and chromosomes 7 and 17 ploidy status. Sequencing of exons 18, 19, and 21 of the EGFR gene for mutations was carried out. Result: For EGFR, 46 (69.7%) of the 66 tumors showed some form of EGFR expression (17 at 3+, 17 at 2+, 12 at 1+) but none gene amplification. Five (9.4%) of 53 tumors showed mutations in exon 18 (n = 3) and exon 19 (n = 2). Polysomy of chromosome 7 (average >2.5 copies/cell) was detected in 15 (25.0%) of 60 tumors (6 at 3+, 5 at 2+, 2 at 1+, 2 at 0+ expression) and correlated with poor 3-year survival (P = 0.015). For HER-2, 17 (25.8%) of 66 tumors expressed HER-2 (10 at 3+, 3 at 2+, 4 at 1+). Eight tumors showed HER-2 gene amplification (6 at 3+, 1 at 1+, 1 at 0+ protein expression). Chromosome 17 polysomy was found in 8 (15.7%) of 51 tumors; two had HER-2 expression (3+, 1+). Conclusion: Our study shows that salivary duct carcinomas (a) harbor EGFR gene mutations in a subset of tumors that may guide therapy, (b) pursue an aggressive clinical course in cases with chromosome 7 polysomy and high EGFR expression, and (c) with HER-2 gene amplification and protein high expression, may be selected for targeted therapy.
机译:目的:唾液管癌过表达表皮生长因子受体(EGFR)和HER-2,尽管其潜在机制尚不清楚。由于这些标记物可能被用作治疗靶标,因此我们通过多种技术评估蛋白质和基因状态,以确定互补值。实验设计:使用66个涎腺导管癌的组织芯片对HER-2和EGFR表达进行免疫组织化学分析(半定量评估为三层系统),并进行荧光原位杂交以检测基因拷贝数以及7号和17号染色​​体状态。进行了EGFR基因外显子18、19和21的突变测序。结果:对于EGFR,66个肿瘤中有46个(69.7%)表现出某种形式的EGFR表达(3+处17、2+处17、1+处12),但无基因扩增。 53个肿瘤中有五个(9.4%)在第18外显子(n = 3)和第19外显子(n = 2)中显示出突变。在60个肿瘤中有15个(25.0%)检测到7号染色体的多态性(平均> 2.5拷贝/细胞)(3+处6个,2 +处5个,1 +处2个,0 +处2个表达)并与3个差年生存率(P = 0.015)。对于HER-2,在66个肿瘤中有17个(25.8%)表达了HER-2(3+时10个,2 +时3个,1 +时4个)。八个肿瘤显示出HER-2基因扩增(蛋白表达3+处6个,蛋白1+处1个,0 +蛋白处1个)。在51个肿瘤中,有8个(15.7%)发现了17号染色​​体多态性; 2个具有HER-2表达(3 +,1 +)。结论:我们的研究表明,涎腺导管癌(a)在可能指导治疗的部分肿瘤中带有EGFR基因突变;(b)在7号染色体多态性和高EGFR表达的病例中采取积极的临床过程;以及(c)可以选择HER-2基因扩增和蛋白质高表达进行靶向治疗。

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