多组学数据分析确定癌症预后生物标志物。

Ezgi Demir Karaman, Zerrin Işık
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引用次数: 1

摘要

使用综合方法将来自不同层面的组学数据结合起来,可以更好地理解癌症等复杂疾病的生物学。与癌症发展或预后相关的生物标志物的发现有助于找到更有效的治疗方案。本研究将不同癌症类型的多组学数据与基于网络的方法相结合,通过在集成网络上运行社区检测方法,探索不同肿瘤之间的共同基因模块。通过几种适应癌症的生物学指标对常见模块进行了评估。然后,通过加权mRNA表达,甲基化和基因突变状态,开发了一种新的预后评分方法。生存分析指出GNG11、CBX2、CDKN3、ARHGEF10、CLN8、SEC61G、PTDSS1基因结果具有统计学意义。文献检索表明,鉴定的生物标志物与相同或不同类型的癌症相关。我们的方法不仅可以识别已知的癌症特异性生物标志物基因,还可以提出新的潜在生物标志物。因此,这项研究为确定新的基因靶点和扩大癌症类型的治疗选择提供了理论依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Multi-Omics Data Analysis Identifies Prognostic Biomarkers across Cancers.

Combining omics data from different layers using integrative methods provides a better understanding of the biology of a complex disease such as cancer. The discovery of biomarkers related to cancer development or prognosis helps to find more effective treatment options. This study integrates multi-omics data of different cancer types with a network-based approach to explore common gene modules among different tumors by running community detection methods on the integrated network. The common modules were evaluated by several biological metrics adapted to cancer. Then, a new prognostic scoring method was developed by weighting mRNA expression, methylation, and mutation status of genes. The survival analysis pointed out statistically significant results for GNG11, CBX2, CDKN3, ARHGEF10, CLN8, SEC61G and PTDSS1 genes. The literature search reveals that the identified biomarkers are associated with the same or different types of cancers. Our method does not only identify known cancer-specific biomarker genes, but also proposes new potential biomarkers. Thus, this study provides a rationale for identifying new gene targets and expanding treatment options across cancer types.

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CiteScore
9.00
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审稿时长
6 weeks
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