Hofele C, Joos S, Flechtenmacher C, Bosch F X, Lichter P, Mühling J, Freier K
Klinik und Poliklinik für Mund-, Kiefer- und Gesichtschirurgie, Universität Heidelberg, Im Neuenheimer Feld 400, 69120 Heidelberg, Germany.
Mund Kiefer Gesichtschir. 2002 Nov;6(6):394-401. doi: 10.1007/s10006-002-0412-5. Epub 2002 Jul 2.
Oral squamous cell carcinomas (OSCC) are malignant tumors with a poor prognosis and low long-term survival rates, even when using modern adjuvant and neoadjuvant therapy forms in addition to surgery. For the clinical estimation of each tumor, it is necessary to define stage-dependent molecular and/or cellular parameters as it is known that OSCC develop along a multistep pathway including the loss of tumor suppressor genes and the amplification of oncogenes which result in changes in protein expression. In order to establish a reliable pattern of molecular and cellular biomarkers, a large number of tumor specimens from different stages of the disease need to be analysed. In this study, biopsies of a collective of 293 OSCC in different stages were screened with the novel technique of tissue chip microarrays by fluorescence in situ hybridization (FISH) and immunohistochemistry (IHC). FISH-analysis was performed on the oncogene cyclin D1 and IHC-analysis on the proteins cyclin D1, p53, p16, cdk4, bcl2, mdm2 and rb. Tissue chip technology was shown to facilitate rapid screening for molecular and cellular alterations in different stages of OSCC and revealed reliable and reproducible results that may allow the definition of a multistep pathway model for tumor progression in OSCC.
口腔鳞状细胞癌(OSCC)是一种预后较差、长期生存率较低的恶性肿瘤,即便在手术之外采用现代辅助和新辅助治疗方式亦是如此。对于每个肿瘤的临床评估而言,有必要定义与分期相关的分子和/或细胞参数,因为已知OSCC是沿着一个多步骤途径发展的,包括肿瘤抑制基因的缺失和癌基因的扩增,这会导致蛋白质表达的改变。为了建立可靠的分子和细胞生物标志物模式,需要分析大量来自疾病不同阶段的肿瘤标本。在本研究中,采用组织芯片微阵列新技术,通过荧光原位杂交(FISH)和免疫组织化学(IHC)对293例不同阶段的OSCC样本进行活检筛查。对癌基因细胞周期蛋白D1进行FISH分析,对细胞周期蛋白D1、p53、p16、细胞周期蛋白依赖性激酶4(cdk4)、bcl2、小鼠双微体2(mdm2)和视网膜母细胞瘤(rb)蛋白进行IHC分析。组织芯片技术被证明有助于快速筛查OSCC不同阶段的分子和细胞改变,并揭示了可靠且可重复的结果,这可能有助于定义OSCC肿瘤进展的多步骤途径模型。