Kopantzev Eugene P, Monastyrskaya Galina S, Vinogradova Tatyana V, Zinovyeva Marina V, Kostina Marya B, Filyukova Olga B, Tonevitsky Alexander G, Sukhikh Gennady T, Sverdlov Eugene D
Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, 16/10 Miklukho-Maklaya, Moscow 117997, Russia.
Lung Cancer. 2008 Oct;62(1):23-34. doi: 10.1016/j.lungcan.2008.02.011. Epub 2008 Apr 3.
We, for the first time, directly compared gene expression profiles in human non-small cell lung carcinomas (NSCLCs) and in human fetal lung development. Previously reported correlations of gene expression profiles between lung cancer and lung development, deduced from matching data on mouse development and human cancer, have brought important information, but suffered from different timing of mouse and human gene expression during fetal development and fundamental differences in tumorigenesis in mice and humans. We used the suppression subtractive hybridization technique to subtract cDNAs prepared from human fetal lung samples at weeks 10-12 and 22-24 and obtained a cDNA library enriched in the transcripts more abundant at the later stage. cDNAs sequencing and RT-PCR analysis of RNAs from human fetal and adult lungs revealed 12 differentially transcribed genes: ADH1B, AQP1, FOLR1, SLC34A2, CAV1, INMT, TXNIP, TPM4, ICAM-1, HLA-DRA, EFNA1 and HLA-E. Most of these genes were found up-regulated in mice and rats at later stages than in human lung development. In surgical samples of NSCLC, these genes were down-regulated as compared to surrounding normal tissues and normal lungs, thus demonstrating opposite expression profiles for the genes up-regulated during fetal lung development.
我们首次直接比较了人类非小细胞肺癌(NSCLC)和人类胎儿肺发育过程中的基因表达谱。先前根据小鼠发育和人类癌症的匹配数据推断出的肺癌与肺发育之间基因表达谱的相关性,带来了重要信息,但在胎儿发育过程中小鼠和人类基因表达的时间不同,以及小鼠和人类肿瘤发生存在根本差异。我们使用抑制性消减杂交技术,从10 - 12周和22 - 24周的人类胎儿肺样本制备的cDNA中进行消减,获得了一个富含后期更丰富转录本的cDNA文库。对人类胎儿和成人肺RNA的cDNA测序和RT-PCR分析揭示了12个差异转录基因:ADH1B、AQP1、FOLR1、SLC34A2、CAV1、INMT、TXNIP、TPM4、ICAM-1、HLA-DRA、EFNA1和HLA-E。这些基因中的大多数在小鼠和大鼠中后期的表达上调,而在人类肺发育中并非如此。在NSCLC手术样本中,与周围正常组织和正常肺相比,这些基因表达下调,从而表明在胎儿肺发育过程中上调的基因具有相反的表达谱。