组织微阵列
头颈部鳞状细胞癌
病理
癌基因
阶段(地层学)
荧光原位杂交
细胞
癌
原发性肿瘤
头颈部癌
生物
头颈部
基因复制
癌症研究
癌症
医学
免疫组织化学
基因
内科学
细胞周期
转移
遗传学
古生物学
外科
染色体
作者
Kolja Freier,Stefan Joos,Christa Flechtenmacher,Frauke Devens,Axel Benner,Franz X. Bosch,Peter Lichter,Christof Hofele
出处
期刊:PubMed
日期:2003-03-15
卷期号:63 (6): 1179-82
被引量:184
摘要
Fluorescence in situ hybridization was applied on a collection of 609 squamous cell carcinomas of the head and neck (HNSCCs),including 511 primary carcinomas of different clinical stage and anatomical localization and 98 recurrent carcinomas, second primary carcinomas, and regional metastases on a tissue microarray. The overall prevalence of amplifications of five oncogenes analyzed was 34.5% for CCND1, 12.7% for EGFR, 8.8% for MYC, 6.2% for ZNF217, and 3.6% for ERBB2. CCND1 amplifications were associated with the pharyngeal site in primary carcinomas (P < 0.001), whereas amplifications of ZNF217 were less frequent in pharyngeal carcinomas as compared with primary oral and laryngeal carcinomas (P = 0.02). The amplification pattern of these oncogenes suggests that different molecular pathways are involved in HNSCCs of different localizations.
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