Mallik Mrinmay Kumar, Majumdar Kaushik, Mujtaba Shiraz
Department of Laboratory Medicine, Mubarak Al Kabeer Hospital, P.O. Box 43787, Hawally 32052, Kuwait.
Department of Pathology, Al Sabah Hospital, P.O. Box 4078, Shuwaikh Industrial 70051, Kuwait.
Brain Sci. 2023 Jan 23;13(2):186. doi: 10.3390/brainsci13020186.
During oncogenesis, alterations in driver genes called driver alterations (DAs) modulate the transcriptome, methylome and proteome through oncogenic signaling pathways. These modulatory effects of any DA may be analyzed by examining differentially expressed mRNAs (DEMs), differentially methylated genes (DMGs) and differentially expressed proteins (DEPs) between tumor samples with and without that DA. We aimed to analyze these modulations with 12 common driver genes in Isocitrate Dehydrogenase 1 wildtype glioblastomas (IDH1-W-GBs). Using Cbioportal, groups of tumor samples with and without DAs in these 12 genes were generated from the IDH1-W-GBs available from "The Cancer Genomics Atlas Firehose Legacy Study Group" (TCGA-FL-SG) on Glioblastomas (GBs). For all 12 genes, samples with and without DAs were compared for DEMs, DMGs and DEPs. We found that DAs in were unassociated with any DEM or DMG in contrast to DAs in all other drivers, which were associated with several DEMs and DMGs. This contrasting -related property of being unassociated with differential gene expression or methylation in IDH1-W-GBs was unaffected by concurrent DAs in other common drivers or by the types of DAs affecting . From the lists of DEMs and DMGs associated with some common drivers other than PTEN, enriched gene ontology terms and insights into the co-regulatory effects of these drivers on the transcriptome were obtained. The findings from this study can improve our understanding of the molecular mechanisms underlying gliomagenesis with potential therapeutic benefits.
在肿瘤发生过程中,被称为驱动改变(DAs)的驱动基因改变通过致癌信号通路调节转录组、甲基化组和蛋白质组。任何一种驱动改变的这些调节作用都可以通过检查具有和不具有该驱动改变的肿瘤样本之间差异表达的mRNA(DEMs)、差异甲基化基因(DMGs)和差异表达蛋白质(DEPs)来进行分析。我们旨在分析异柠檬酸脱氢酶1野生型胶质母细胞瘤(IDH1-W-GBs)中12个常见驱动基因的这些调节作用。利用cbioportal,从“癌症基因组图谱消防水带遗留研究组”(TCGA-FL-SG)提供的胶质母细胞瘤(GBs)的IDH1-W-GBs中生成了这12个基因具有和不具有驱动改变的肿瘤样本组。对于所有12个基因,比较了具有和不具有驱动改变的样本的DEMs、DMGs和DEPs。我们发现,与所有其他驱动基因的驱动改变不同,[此处原文缺失具体基因名称]的驱动改变与任何DEM或DMG均无关联;而所有其他驱动基因的驱动改变均与多个DEM和DMG相关。在IDH1-W-GBs中,这种与差异基因表达或甲基化无关联的对比相关特性不受其他常见驱动基因同时发生的驱动改变或影响[此处原文缺失具体基因名称]的驱动改变类型的影响。从与除PTEN之外的一些常见驱动基因相关的DEMs和DMGs列表中,获得了丰富的基因本体术语以及对这些驱动基因对转录组的共同调节作用的深入了解。本研究结果可增进我们对胶质瘤发生潜在分子机制的理解,并具有潜在的治疗益处。