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头颈部鳞状细胞癌中不同位点特异性癌蛋白的过表达:一项组织芯片分析

Distinct site-specific oncoprotein overexpression in head and neck squamous cell carcinoma: a tissue microarray analysis.

作者信息

Freier Kolja, Bosch Franz X, Flechtenmacher Christa, Devens Frauke, Benner Axel, Lichter Peter, Joos Stefan, Hofele Christof

机构信息

Deutsches Krebsforschungszentrum, Abt. Molekulare Genetik (H0700), TP3, D-69120 Heidelberg, Germany.

出版信息

Anticancer Res. 2003 Sep-Oct;23(5A):3971-7.

Abstract

BACKGROUND

Tissue microarray (TMA) analysis is a high-throughput approach that allows the screening of large tumor collectives for cytogenetic aberrrations. In this study, a TMA of a large collection of clinically well-defined primary squamous cell carcinomas of the head and neck (HNSCC) was used to determine the expression of several oncoproteins.

MATERIALS AND METHODS

A TMA containing 547 primary HNSCC was used for the analysis of cyclinD1, c-myc, erbb1 and erbb2 expression by immunohistochemistry (IHC).

RESULTS

CyclinD1 and c-myc were overexpressed at higher frequencies in primary pharyngeal and laryngeal carcinomas compared with primary oral carcinomas (p < 0.001 and p < 0.001), while erbb1 and erbb2 overexpression was associated with oral site (p < 0.001 and p = 0.04, respectively). Furthermore, cyclinD1 overexpression correlated with stage IV primary carcinomas (p = 0.04).

CONCLUSION

HNSCC is a heterogenous group of tumors, which, depending on anatomic sites and clinical stage, shows variable expressions of the oncoproteins described. This indicates a specific pathogenic role of these oncoproteins in different subtypes of HNSCC and may have therapeutic implications.

摘要

背景

组织微阵列(TMA)分析是一种高通量方法,可用于筛查大量肿瘤样本中的细胞遗传学异常。在本研究中,使用了一个包含大量临床明确的头颈部原发性鳞状细胞癌(HNSCC)的TMA来确定几种癌蛋白的表达。

材料与方法

使用一个包含547例原发性HNSCC的TMA,通过免疫组织化学(IHC)分析细胞周期蛋白D1、c-myc、表皮生长因子受体1(erbb1)和表皮生长因子受体2(erbb2)的表达。

结果

与原发性口腔癌相比,原发性咽癌和喉癌中细胞周期蛋白D1和c-myc的过表达频率更高(p < 0.001和p < 0.001),而erbB1和erbB2的过表达与口腔部位相关(分别为p < 0.001和p = 0.04)。此外,细胞周期蛋白D1过表达与IV期原发性癌相关(p = 0.04)。

结论

HNSCC是一组异质性肿瘤,根据解剖部位和临床分期,所描述的癌蛋白表达存在差异。这表明这些癌蛋白在HNSCC的不同亚型中具有特定的致病作用,可能具有治疗意义。

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