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首页> 外文期刊>International journal of biological sciences >Varied Pathways of Stage IA Lung Adenocarcinomas Discovered by Integrated Gene Expression Analysis
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Varied Pathways of Stage IA Lung Adenocarcinomas Discovered by Integrated Gene Expression Analysis

机译:综合基因表达分析发现IA期肺腺癌的多种途径

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Background: Discovery of the progression-associated genes and pathways in lung adenocarcinoma (LAD) has important implications in understanding the molecular mechanism of tumor development. However, few studies had been performed to focus on the changes of pathways in lung adenocarcinoma development using microarray expression profile. Result: We performed a meta-analysis of 4 LAD microarray datasets encompassing 353 patients to reveal differentially expressed genes (DEGs) between normal lung tissues and LAD of different stages. Overall, 1 838 genes were found to be dys-regulated, and the adipogenesis, circadian rhythm, and Id pathways were significantly changed. Interestingly, most of the genes from the same gene family (such as Interleukin receptor, Matrix metallopeptidase, Histone cluster and Minichromosome maintenance complex component families) were found to be up-regulated (or down-regulated). Real-time PCR (qRT-PCR) was applied to validate the expression of randomly selected 18 DEGs in LAD cell lines. In the pathway analysis among stages, Oxidative stress, Glycolysis/Gluconeogenesis and Integrin-mediated cell adhesion pathways, which were involved in cancer cell proliferation and metastasis, were showed to be significantly regulated in stages other than IA. Conclusion: Genes involved in adipogenesis and Id pathways might play important roles in development of LADs. The similar trend of expression of the gene family members suggested coordinate regulation in tumor progression. Three pathways (Oxidative stress, Glycolysis/Gluconeogenesis and Integrin-mediated cell adhesion pathways) significantly regulated in stages other than stage IA suggested that genes and pathways conferring invasive character might be activated in the preinvasive stage IB, while the Oxidative stress and the Glycolysis/Gluconeogenesis pathways might have strong connections to cisplatin-based chemotherapy. The insignificantly regulated three pathways in stage IA might be used in early-stage detection of LAD.
机译:背景:肺腺癌(LAD)中与进展相关的基因和途径的发现对于理解肿瘤发展的分子机制具有重要意义。然而,很少有研究使用微阵列表达谱来关注肺腺癌发生发展的途径变化。结果:我们对涵盖353名患者的4个LAD微阵列数据集进行了荟萃分析,以揭示正常肺组织和不同阶段LAD之间的差异表达基因(DEG)。总体而言,发现1838个基因被异常调节,并且脂肪形成,昼夜节律和Id途径发生了显着变化。有趣的是,发现来自同一基因家族的大多数基因(例如白介素受体,基质金属肽酶,组蛋白簇和微染色体维持复合物组分家族)被上调(或下调)。应用实时PCR(qRT-PCR)验证LAD细胞系中随机选择的18个DEG的表达。在各阶段之间的途径分析中,氧化应激,糖酵解/糖异生和整合素介导的细胞粘附途径(与癌细胞增殖和转移有关)在除IA以外的其他阶段均受到显着调节。结论:参与脂肪形成和Id途径的基因可能在LAD的发展中起重要作用。基因家族成员表达的相似趋势表明肿瘤进展中的协调调节。除IA期外,其他三个阶段(氧化应激,糖酵解/糖异生和整合素介导的细胞粘附途径)均受到显着调节,这表明在IB浸润前阶段可能激活了赋予侵袭性的基因和途径,而氧化应激和糖酵解/糖异生途径可能与基于顺铂的化学疗法有很强的联系。 IA阶段中微不足道的三个途径可用于LAD的早期检测。

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