Modeling the relationship between gene expression and mutational signature.

Pub Date : 2023-03-01 DOI:10.15302/j-qb-022-0309
Limin Jiang, Hui Yu, Yan Guo
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引用次数: 1

Abstract

Background: Mutational signatures computed from somatic mutations, allow an in-depth understanding of tumorigenesis and may illuminate early prevention strategies. Many studies have shown the regulation effects between somatic mutation and gene expression dysregulation.

Methods: We hypothesized that there are potential associations between mutational signature and gene expression. We capitalized upon RNA-seq data to model 49 established mutational signatures in 33 cancer types. Both accuracy and area under the curve were used as performance measures in five-fold cross-validation.

Results: A total of 475 models using unconstrained genes, and 112 models using protein-coding genes were selected for future inference purposes. An independent gene expression dataset on lung cancer smoking status was used for validation which achieved over 80% for both accuracy and area under the curve.

Conclusion: These results demonstrate that the associations between gene expression and somatic mutations can translate into the associations between gene expression and mutational signatures.

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基因表达与突变特征之间的关系建模。
背景:体细胞突变计算的突变特征,允许深入了解肿瘤发生,并可能阐明早期预防策略。许多研究表明体细胞突变与基因表达失调之间存在调控作用。方法:我们假设突变特征和基因表达之间存在潜在的关联。我们利用RNA-seq数据对33种癌症类型中的49个已建立的突变特征进行建模。准确度和曲线下面积作为五重交叉验证的性能指标。结果:共选择了475个使用无约束基因的模型,以及112个使用蛋白质编码基因的模型,用于未来的推断。使用独立的肺癌吸烟状态基因表达数据集进行验证,其准确性和曲线下面积均达到80%以上。结论:这些结果表明,基因表达与体细胞突变之间的关系可以转化为基因表达与突变特征之间的关系。
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