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人类支气管鳞状细胞癌发生过程中微小RNA表达的演变

Evolution of microRNA expression during human bronchial squamous carcinogenesis.

作者信息

Mascaux C, Laes J F, Anthoine G, Haller A, Ninane V, Burny A, Sculier J P

机构信息

Institut Jules Bordet, Rue Héger-Bordet 1, B-1000 Brussels, Belgium.

出版信息

Eur Respir J. 2009 Feb;33(2):352-9. doi: 10.1183/09031936.00084108. Epub 2008 Nov 14.

Abstract

MicroRNAs, negative post-transcriptional regulators of gene expression, are involved in cancer. Their role in early bronchial carcinogenesis was analysed in 60 biopsies obtained by fluorescence bronchoscopy (six per stage: normal tissue of nonsmokers, normal normofluorescent and hypofluorescent bronchial tissue of smokers, hyperplasia, metaplasia, mild, moderate and severe dysplasia, in situ carcinoma and invasive squamous cell carcinoma (SQCC)). In total, 69 microRNAs were found to be differentially expressed in the course of bronchial carcinogenesis. Among them, some microRNAs showed a linear evolution of their expression level, such as miR-32 and miR-34c, whose expression progressively decreased from normal bronchial tissues of nonsmokers to SQCC. Others behaved differently at successive stages, such as miR-142-3p or miR-9, or are only altered from a specific stage, such as miR-199a or miR-139. MicroRNAs globally followed a two-step evolution, first decreasing (a reverse of their increase during embryogenesis) during the earliest morphological modifications of bronchial epithelium, and thereafter increasing at later stages of lung carcinogenesis. Moreover, microRNA expression was very efficient for the prediction of the histological classification between low- and high-grade lesions and between in situ and invasive carcinoma. The present data show, for the first time, that microRNAs are involved in bronchial carcinogenesis from the very early steps of this process and, thus, could provide tools for early detection of lung cancer.

摘要

微小RNA作为基因表达的负性转录后调节因子,与癌症相关。通过荧光支气管镜检查获取60份活检组织(每个阶段6份:非吸烟者的正常组织、吸烟者的正常正常荧光和低荧光支气管组织、增生、化生、轻度、中度和重度发育异常、原位癌和浸润性鳞状细胞癌(SQCC)),分析了它们在早期支气管癌发生中的作用。总共发现69种微小RNA在支气管癌发生过程中差异表达。其中,一些微小RNA的表达水平呈线性变化,如miR-32和miR-34c,其表达从非吸烟者的正常支气管组织到SQCC逐渐降低。其他的在连续阶段表现不同,如miR-142-3p或miR-9,或者仅在特定阶段发生改变,如miR-199a或miR-139。微小RNA总体上遵循两步演变,首先在支气管上皮最早的形态学改变期间降低(与胚胎发育期间的增加相反),然后在肺癌发生的后期增加。此外,微小RNA表达对于预测低级别和高级别病变之间以及原位癌和浸润癌之间的组织学分类非常有效。目前的数据首次表明,微小RNA在支气管癌发生的早期阶段就参与其中,因此可为肺癌的早期检测提供工具。

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