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支气管发育异常中c-ErbB1/表皮生长因子受体和c-ErbB2/HER-2表达的分析:肺癌化学预防潜在靶点的评估

Analysis of c-ErbB1/epidermal growth factor receptor and c-ErbB2/HER-2 expression in bronchial dysplasia: evaluation of potential targets for chemoprevention of lung cancer.

作者信息

Merrick Daniel T, Kittelson John, Winterhalder Ralph, Kotantoulas Georgia, Ingeberg Steen, Keith Robert L, Kennedy Timothy C, Miller York E, Franklin Wilbur A, Hirsch Fred R

机构信息

Department of Pathology, University of Colorado Cancer Center, Denver, Colorado, USA.

出版信息

Clin Cancer Res. 2006 Apr 1;12(7 Pt 1):2281-8. doi: 10.1158/1078-0432.CCR-05-2291.

Abstract

PURPOSE

Lung cancer is preceded by a premalignant phase during which intervention could decrease associated morbidity and mortality. Molecular characterization of factors involved in controlling progression of bronchial dysplasias will provide markers of premalignant change and identify targets for chemoprevention.

EXPERIMENTAL DESIGN

Immunohistochemical analysis of epidermal growth factor receptor (EGFR; c-ErbB1/EGFR), HER-2/neu (c-ErbB2/HER-2), Ki-67, and minichromosome maintenance protein 2 (MCM2) expression in bronchial dysplasia was undertaken to characterize molecular alterations associated with the progression of these lesions in 268 bronchoscopically obtained biopsies from 134 subjects.

RESULTS

Analysis of biopsies with the most severe diagnosis from each subject showed a linear relationship between increasing marker expression and severity of dysplastic change for EGFR (P < 0.001), Ki-67 (P < 0.001), and MCM2 (P = 0.001) but not HER-2 (P = 0.102). Increased expression of either EGFR or HER-2 was associated with increased levels of Ki-67 and MCM2 expression, and combined overexpression of these receptors was associated with the highest levels of proliferation, suggesting a synergistic effect. Finally, the lack of an associated trend toward increased EGFR expression when comparing the worst and best biopsies within each subject indicated a potential field effect in the induction of EGFR expression.

CONCLUSIONS

The results suggest a prominent role for EGFR overexpression in the development and progression of bronchial dysplasia and provide rationale for exploring inhibition of EGFR signaling in lung cancer chemoprevention.

摘要

目的

肺癌之前存在一个癌前阶段,在此阶段进行干预可降低相关的发病率和死亡率。对参与控制支气管发育异常进展的因素进行分子特征分析,将提供癌前变化的标志物,并确定化学预防的靶点。

实验设计

对134名受试者经支气管镜获取的268份活检组织中的支气管发育异常进行表皮生长因子受体(EGFR;c-ErbB1/EGFR)、HER-2/neu(c-ErbB2/HER-2)、Ki-67和微小染色体维持蛋白2(MCM2)表达的免疫组织化学分析,以表征与这些病变进展相关的分子改变。

结果

对每个受试者诊断最严重的活检组织进行分析,结果显示EGFR(P < 0.001)、Ki-67(P < 0.001)和MCM2(P = 0.001)的标志物表达增加与发育异常变化的严重程度之间存在线性关系,而HER-2(P = 0.102)则不存在。EGFR或HER-2表达增加与Ki-67和MCM2表达水平升高相关,这些受体的联合过表达与最高水平的增殖相关,提示存在协同效应。最后,在比较每个受试者中最差和最好的活检组织时,EGFR表达缺乏相关的增加趋势,这表明在EGFR表达诱导中存在潜在的场效应。

结论

结果表明EGFR过表达在支气管发育异常的发生和进展中起重要作用,并为探索在肺癌化学预防中抑制EGFR信号传导提供了理论依据。

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