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在肺癌发生过程中表达的微小RNA在人类假腺期肺胚胎发育过程中也有表达。

MicroRNAs expressed during lung cancer development are expressed in human pseudoglandular lung embryogenesis.

作者信息

Navarro Alfons, Marrades Ramon M, Viñolas Nuria, Quera Angels, Agustí Carlos, Huerta Arturo, Ramirez Jose, Torres Antoni, Monzo Mariano

机构信息

Human Anatomy and Embryology, School of Medicine, University of Barcelona, Barcelona, Spain.

出版信息

Oncology. 2009;76(3):162-9. doi: 10.1159/000201569. Epub 2009 Feb 11.

DOI:10.1159/000201569
PMID:19209007
Abstract

BACKGROUND/AIMS: MicroRNAs (miRNAs) play a role during mouse embryonic development and are also important in carcinogenesis. In order to investigate whether there are similar patterns of miRNA expression levels in pseudoglandular human embryonic lung and in human lung tumors, we have analyzed 18 miRNAs (the let-7 family, the miR-17-92 cluster, miR-221 and miR-222) in human embryonic lung samples and in paired lung tumor and normal lung tissue samples and correlated the results with clinicopathological characteristics.

METHODS

RNA was obtained from 12 human embryonic lung samples, 33 lung tumor samples and 33 paired normal lung samples. miRNAs were assessed by quantitative real-time PCR.

RESULTS

Members of the let-7 family were downregulated and members of the miR-17-92 cluster and miR-221 were overexpressed both in embryonic lung tissue and in lung tumors. Low levels of let-7c were associated with absence of metastases (p = 0.015), early-stage non-small cell lung cancer (NSCLC, p = 0.05), and smokers (p = 0.009). High levels of miR-106a were associated with small-cell lung cancer (p = 0.031), and high levels of miR-19a with advanced NSCLC (p = 0.008).

CONCLUSION

Our study lends support to the model of cancer as an alteration of normal development, as many miRNAs were similarly expressed in early human lung development and stage I-II of lung cancer development.

摘要

背景/目的:微小RNA(miRNA)在小鼠胚胎发育过程中发挥作用,在肿瘤发生中也很重要。为了研究在人胚胎肺假腺期和人肺肿瘤中是否存在相似的miRNA表达水平模式,我们分析了18种miRNA(let-7家族、miR-17-92簇、miR-221和miR-222)在人胚胎肺样本、配对的肺肿瘤和正常肺组织样本中的表达,并将结果与临床病理特征进行关联分析。

方法

从12个人胚胎肺样本、33个肺肿瘤样本和33个配对的正常肺样本中获取RNA。通过定量实时PCR评估miRNA。

结果

let-7家族成员在胚胎肺组织和肺肿瘤中均下调,miR-17-92簇成员和miR-221均过表达。低水平的let-7c与无转移(p = 0.015)、早期非小细胞肺癌(NSCLC,p = 0.05)和吸烟者(p = 0.009)相关。高水平的miR-106a与小细胞肺癌相关(p = 0.031),高水平的miR-19a与晚期NSCLC相关(p = 0.008)。

结论

我们的研究支持癌症是正常发育改变的模型,因为许多miRNA在人肺早期发育和肺癌发展的I-II期有相似的表达。

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