Division of Clinical Cancer Epidemiology, Department of Oncology, Institute of Clinical Sciences, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden ; Department of Oncology, Institute of Clinical Sciences, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.
Department of Oncology, Institute of Clinical Sciences, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.
Comput Math Methods Med. 2013;2013:413783. doi: 10.1155/2013/413783. Epub 2013 Dec 18.
DNA copy number aberrations (DCNA) and subsequent altered gene expression profiles may have a major impact on tumor initiation, on development, and eventually on recurrence and cancer-specific mortality. However, most methods employed in integrative genomic analysis of the two biological levels, DNA and RNA, do not consider survival time. In the present note, we propose the adoption of a survival analysis-based framework for the integrative analysis of DCNA and mRNA levels to reveal their implication on patient clinical outcome with the prerequisite that the effect of DCNA on survival is mediated by mRNA levels. The specific aim of the paper is to offer a feasible framework to test the DCNA-mRNA-survival pathway. We provide statistical inference algorithms for mediation based on asymptotic results. Furthermore, we illustrate the applicability of the method in an integrative genomic analysis setting by using a breast cancer data set consisting of 141 invasive breast tumors. In addition, we provide implementation in R.
DNA 拷贝数异常(DCNA)和随后的基因表达谱改变可能对肿瘤的发生、发展,最终对复发和癌症特异性死亡率有重大影响。然而,在对 DNA 和 RNA 这两个生物学水平进行综合基因组分析中所采用的大多数方法都没有考虑生存时间。在本说明中,我们建议采用基于生存分析的框架来综合分析 DCNA 和 mRNA 水平,以揭示它们对患者临床结果的影响,前提是 DCNA 对生存的影响是由 mRNA 水平介导的。本文的具体目的是提供一个可行的框架来检验 DCNA-mRNA-生存途径。我们提供了基于渐近结果的中介统计推断算法。此外,我们通过使用包含 141 例浸润性乳腺癌的乳腺癌数据集,说明了该方法在综合基因组分析中的适用性。此外,我们还在 R 中提供了实现。