Veith Thomas, Beck Richard, Brown Joel S, Andor Noemi
Integrated Mathematical Oncology, H. Lee Moffitt Cancer Center, 12902 USF Magnolia Drive, Tampa, FL 33612, USA.
Department of Molecular Biosciences, University of South Florida, 4202 E Fowler Ave, Tampa, FL 33612, USA.
bioRxiv. 2025 Apr 7:2025.03.23.644809. doi: 10.1101/2025.03.23.644809.
Chromosomal instability (CIN), characterized by pervasive copy number alterations (CNAs), significantly contributes to cancer progression and therapeutic resistance. CNAs drive intratumoral genetic heterogeneity, creating distinct subpopulations whose interactions shape tumor evolution through frequency-dependent selection. Here, we introduce, ECO-K (Ecological-Karyotypes), an inverse game theory framework that infers subpopulation interactions from longitudinal single-cell whole genome sequencing data. Applying this approach to serially-passaged, triple-negative breast cancer (TNBC) cell lines and patient-derived xenografts (PDXs), we systematically identified frequency-dependent selection dynamics governed by karyotypic diversity. Notably, in one PDX lineage, we found consistent evidence of karyotypically defined subpopulations acting as interaction hubs, associated specifically with chromosome 1 loss and chromosome 14p gain. Our framework provides testable predictions of intratumoral ecological dynamics, highlighting opportunities to strategically target key subpopulations to disrupt tumor evolution.
染色体不稳定(CIN)以广泛的拷贝数改变(CNA)为特征,对癌症进展和治疗耐药性有显著影响。CNA驱动肿瘤内遗传异质性,产生不同的亚群,其相互作用通过频率依赖性选择塑造肿瘤进化。在此,我们引入了ECO-K(生态核型),这是一种逆向博弈论框架,可从纵向单细胞全基因组测序数据推断亚群相互作用。将该方法应用于连续传代的三阴性乳腺癌(TNBC)细胞系和患者来源的异种移植瘤(PDX),我们系统地确定了由核型多样性控制的频率依赖性选择动态。值得注意的是,在一个PDX谱系中,我们发现了一致的证据,表明核型定义的亚群作为相互作用枢纽,特别与1号染色体缺失和14号染色体短臂增加有关。我们的框架提供了对肿瘤内生态动态的可测试预测,突出了战略性靶向关键亚群以破坏肿瘤进化的机会。