摘要
目的:检测作为当前靶向治疗中的生物抑制剂EGFR,c-Met和HER2/neu3种抗体在12例脊索瘤中的表达。方法:对12例脊索瘤和包含17种其他肿瘤(共51个样本)的多肿瘤组织阵列切片进行免疫组化法的蛋白表达以及相关分析。结果:大多数脊索瘤显示EGFR和C-Met的过度表达,而c-Erb-B2的表达差异较大,并且EGFR和C-Met的表达存在显著的关联性(P=0.006)。结论:脊索瘤像其他实体瘤一样,也表达EGFR,c-Met和HER2/neu3种抗体,大部分脊索瘤对EGFR和C-Met的表达程度较高。EGFR抑制剂已在其他实体瘤进行临床试验,并为进行顽固性脊索瘤临床试验提供了理论依据。
Objective: To investigate the expression of c-Met, c-Erb-b2 and EGFR in 12 chordomas, based on the current and future availabihty of targeted molecular inhibitors. Method: Protein expression levels were analyzed by inmmnohistochemi analysis from 12 chordomas and 51 other tumors from 17 assorted solid tissue tumor types using multitumored tissue microarray. Results: Most chordomas displayed strong expression of EGFR and c-Met, while a variable level of expression of HER2/neu was observed. In addition, we noted a strong correlation between EGFR and c-Met expression, especially for primary chordomas (P = 0.006). Conclusiol~: Chordoma, like many other solid-tissue tumors, expresses HER2/neu, EGFR and c-Met. Most chordoma has strong expression of both c-Met and EGFR. Inhibitors to EGFR are already in clinical use for other solid tissue tumors and represent a potentially viable experimental treatment option for refractory chordoma.
出处
《山东大学耳鼻喉眼学报》
CAS
2006年第6期488-492,共5页
Journal of Otolaryngology and Ophthalmology of Shandong University
基金
美国耶鲁大学OHSE基金会基金(1334715)
关键词
脊索瘤
受体酪氨酸激酶
靶向治疗
免疫组化
Chordoma
Receptor tyrosine kinase
Targeted therapy
Immunohistochemistry