UniSA STEM Unit, University of South Australia, Mawson Lakes Blvd, 5095, South Australia , Australia.
Brief Funct Genomics. 2022 Nov 17;21(6):455-465. doi: 10.1093/bfgp/elac030.
The traditional way for discovering genes which drive cancer (namely cancer drivers) neglects the dynamic information of cancer development, even though it is well known that cancer progresses dynamically. To enhance cancer driver discovery, we expand cancer driver concept to dynamic cancer driver as a gene driving one or more bio-pathological transitions during cancer progression. Our method refers to the fact that cancer should not be considered as a single process but a compendium of altered biological processes causing the disease to develop over time. Reciprocally, different drivers of cancer can potentially be discovered by analysing different bio-pathological pathways. We propose a novel approach for causal inference of genes driving one or more core processes during cancer development (i.e. dynamic cancer driver). We use the concept of pseudotime for inferring the latent progression of samples along a biological transition during cancer and identifying a critical event when such a process is significantly deviated from normal to carcinogenic. We infer driver genes by assessing the causal effect they have on the process after such a critical event. We have applied our method to single-cell and bulk sequencing datasets of breast cancer. The evaluation results show that our method outperforms well-recognized cancer driver inference methods. These results suggest that including information of the underlying dynamics of cancer improves the inference process (in comparison with using static data), and allows us to discover different sets of driver genes from different processes in cancer. R scripts and datasets can be found at https://github.com/AndresMCB/DynamicCancerDriver.
传统的发现驱动癌症(即癌症驱动基因)的方法忽略了癌症发展的动态信息,尽管众所周知癌症是动态发展的。为了增强癌症驱动基因的发现,我们将癌症驱动基因的概念扩展为动态癌症驱动基因,即一个基因在癌症进展过程中驱动一个或多个生物病理转变。我们的方法是基于这样一个事实,即癌症不应被视为单一的过程,而是一系列导致疾病随时间发展的改变了的生物学过程的综合。相反,通过分析不同的生物病理途径,有可能发现不同的癌症驱动基因。我们提出了一种新的方法,用于推断在癌症发展过程中驱动一个或多个核心过程(即动态癌症驱动基因)的基因。我们使用伪时间的概念来推断样本在癌症过程中的生物转变过程中的潜在进展,并确定当这样一个过程显著偏离正常向致癌时的一个关键事件。我们通过评估这些基因在关键事件后对该过程的因果效应来推断驱动基因。我们已经将我们的方法应用于乳腺癌的单细胞和批量测序数据集。评估结果表明,我们的方法优于公认的癌症驱动基因推断方法。这些结果表明,包括癌症潜在动力学的信息可以改进推断过程(与使用静态数据相比),并允许我们从癌症的不同过程中发现不同的驱动基因集。R 脚本和数据集可以在 https://github.com/AndresMCB/DynamicCancerDriver 上找到。