Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Am J Hum Genet. 2024 Feb 1;111(2):227-241. doi: 10.1016/j.ajhg.2023.12.009. Epub 2024 Jan 16.
Distinguishing genomic alterations in cancer-associated genes that have functional impact on tumor growth and disease progression from the ones that are passengers and confer no fitness advantage have important clinical implications. Evidence-based methods for nominating drivers are limited by existing knowledge on the oncogenic effects and therapeutic benefits of specific variants from clinical trials or experimental settings. As clinical sequencing becomes a mainstay of patient care, applying computational methods to mine the rapidly growing clinical genomic data holds promise in uncovering functional candidates beyond the existing knowledge base and expanding the patient population that could potentially benefit from genetically targeted therapies. We propose a statistical and computational method (MAGPIE) that builds on a likelihood approach leveraging the mutual exclusivity pattern within an oncogenic pathway for identifying probabilistically both the specific genes within a pathway and the individual mutations within such genes that are truly the drivers. Alterations in a cancer-associated gene are assumed to be a mixture of driver and passenger mutations with the passenger rates modeled in relationship to tumor mutational burden. We use simulations to study the operating characteristics of the method and assess false-positive and false-negative rates in driver nomination. When applied to a large study of primary melanomas, the method accurately identifies the known driver genes within the RTK-RAS pathway and nominates several rare variants as prime candidates for functional validation. A comprehensive evaluation of MAGPIE against existing tools has also been conducted leveraging the Cancer Genome Atlas data.
区分癌症相关基因中的基因组改变,这些改变对肿瘤生长和疾病进展有功能影响,与那些没有适应优势的乘客基因不同,具有重要的临床意义。基于证据的提名驱动基因的方法受到临床试验或实验环境中特定变异的致癌效应和治疗益处的现有知识的限制。随着临床测序成为患者治疗的主要手段,应用计算方法挖掘快速增长的临床基因组数据有望在现有知识库之外发现功能候选基因,并扩大可能受益于基因靶向治疗的患者群体。我们提出了一种统计和计算方法(MAGPIE),该方法基于一种似然方法,利用致癌途径中的互斥模式,概率性地确定途径中的特定基因以及此类基因中的单个突变,这些突变才是真正的驱动因素。癌症相关基因的改变被假设为驱动突变和乘客突变的混合物,乘客率与肿瘤突变负担相关。我们使用模拟来研究该方法的工作特性,并评估驱动基因提名中的假阳性和假阴性率。当应用于对原发性黑色素瘤的大型研究时,该方法准确地识别了 RTK-RAS 途径中的已知驱动基因,并提名了几个罕见变体作为功能验证的主要候选基因。还利用癌症基因组图谱数据对 MAGPIE 与现有工具进行了全面评估。