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DORGE: Discovery of Oncogenes and tumoR suppressor genes using Genetic and Epigenetic features

机译:Dorge:使用遗传和表观遗传特征发现癌肠和肿瘤抑制基因

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Data-driven discovery of cancer driver genes, including tumor suppressor genes (TSGs) and oncogenes (OGs), is imperative for cancer prevention, diagnosis, and treatment. Although epigenetic alterations are important for tumor initiation and progression, most known driver genes were identified based on genetic alterations alone. Here, we developed an algorithm, DORGE (Discovery of Oncogenes and tumor suppressoR genes using Genetic and Epigenetic features), to identify TSGs and OGs by integrating comprehensive genetic and epigenetic data. DORGE identified histone modifications as strong predictors for TSGs, and it found missense mutations, super enhancers, and methylation differences as strong predictors for OGs. We extensively validated DORGE-predicted cancer driver genes using independent functional genomics data. We also found that DORGE-predicted dual-functional genes (both TSGs and OGs) are enriched at hubs in protein-protein interaction and drug-gene networks. Overall, our study has deepened the understanding of epigenetic mechanisms in tumorigenesis and revealed previously undetected cancer driver genes.
机译:数据驱动的癌症驾驶基因的发现,包括肿瘤抑制基因(TSG)和癌基因(OGS),对癌症预防,诊断和治疗是必不可少的。虽然表观遗传改变对于肿瘤引发和进展很重要,但基于单独的遗传改变鉴定了最着名的驾驶基因。在这里,我们开发了一种算法,通过整合综合遗传和表观遗传数据来鉴定TSG和OGS的算法Dorge(发现癌细胞和肿瘤抑制基因)。 Dorge将组蛋白修饰确定为TSGS的强预测因子,它发现了畸形突变,超强增强剂和甲基化差异,作为OG的强预测因子。我们使用独立的功能基因组学数据广泛验证了Dorge预测的癌症司机基因。我们还发现Dorge预测的双官能基因(Tsgs和OGS)在蛋白质 - 蛋白质相互作用和药物基因网络中富集。总体而言,我们的研究深化了对肿瘤发生中的表观遗传机制的理解,并揭示了先前未检测到的癌症驾驶员基因。

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