Department of Research, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Platform of Integrated Biology, Department of Applied Research and Technology Development, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Sci Rep. 2019 Sep 10;9(1):13039. doi: 10.1038/s41598-019-49648-2.
Alterations in the gene expression of organs in contact with the environment may signal exposure to toxins. To identify genes in lung tissue whose expression levels are altered by cigarette smoking, we compared the transcriptomes of lung tissue between 118 ever smokers and 58 never smokers. In all cases, the tissue studied was non-involved lung tissue obtained at lobectomy from patients with lung adenocarcinoma. Of the 17,097 genes analyzed, 357 were differentially expressed between ever smokers and never smokers (FDR < 0.05), including 290 genes that were up-regulated and 67 down-regulated in ever smokers. For 85 genes, the absolute value of the fold change was ≥2. The gene with the smallest FDR was MYO1A (FDR = 6.9 × 10) while the gene with the largest difference between groups was FGG (fold change = 31.60). Overall, 100 of the genes identified in this study (38.6%) had previously been found to associate with smoking in at least one of four previously reported datasets of non-involved lung tissue. Seven genes (KMO, CD1A, SPINK5, TREM2, CYBB, DNASE2B, FGG) were differentially expressed between ever and never smokers in all five datasets, with concordant higher expression in ever smokers. Smoking-induced up-regulation of six of these genes was also observed in a transcription dataset from lung tissue of non-cancer patients. Among the three most significant gene networks, two are involved in immunity and inflammation and one in cell death. Overall, this study shows that the lung parenchyma transcriptome of smokers has altered gene expression and that these alterations are reproducible in different series of smokers across countries. Moreover, this study identified a seven-gene panel that reflects lung tissue exposure to cigarette smoke.
与环境接触的器官的基因表达改变可能表明暴露于毒素。为了鉴定吸烟引起的肺组织中基因表达改变的基因,我们比较了 118 例曾吸烟者和 58 例从不吸烟者的肺组织转录组。在所有情况下,研究的组织均为肺腺癌患者肺叶切除术中获得的非病变肺组织。在分析的 17097 个基因中,有 357 个在曾吸烟者和从不吸烟者之间表达水平差异有统计学意义(FDR < 0.05),包括 290 个上调和 67 个下调的基因。对于 85 个基因,倍数变化的绝对值≥2。FDR 最小的基因是 MYO1A(FDR = 6.9 × 10),而两组间差异最大的基因是 FGG(倍数变化 = 31.60)。总的来说,在这项研究中鉴定的 100 个基因(38.6%)在之前四个非病变肺组织数据集的至少一个中与吸烟有关。七个基因(KMO、CD1A、SPINK5、TREM2、CYBB、DNASE2B、FGG)在所有五个数据集中在曾吸烟者和从不吸烟者之间表达差异有统计学意义,曾吸烟者表达更高。在非癌症患者肺组织的转录组数据集中也观察到这六个基因的吸烟诱导上调。在三个最重要的基因网络中,有两个与免疫和炎症有关,一个与细胞死亡有关。总的来说,这项研究表明,吸烟者的肺实质转录组基因表达发生改变,并且这些改变在不同国家的不同系列吸烟者中是可重现的。此外,本研究确定了一个反映肺组织暴露于香烟烟雾的七基因组合。