Hematology Department, Institut Curie, Saint Cloud, France; University PSL, Inserm U1288, Laboratoire d'Imagerie Translationnelle en Oncologie, 91400 Orsay, France.
Department of Molecular Oncology, British Columbia Cancer, Vancouver, BC, Canada.
Cancer Cell. 2024 Jun 10;42(6):1003-1017.e6. doi: 10.1016/j.ccell.2024.05.011.
Histological transformation of follicular lymphoma (FL) to aggressive forms is associated with poor outcome. Phenotypic consequences of this evolution and its impact on the tumor microenvironment (TME) remain unknown. We perform single-cell whole genome sequencing (scWGS) and transcriptome sequencing (scWTS) of 11 paired pre/post-transformation patient samples and scWTS of additional samples from patients without transformation. Our analysis reveals evolutionary dynamics of transformation at single-cell resolution, highlighting a shifting TME landscape, with an emerging immune-cell exhaustion signature, co-evolving with the shifting malignant B phenotype in a regulatory ecosystem. Integration of scWGS and scWTS identifies malignant cell pathways upregulated during clonal tumor evolution. Using multi-color immunofluorescence, we transfer these findings to a TME-based transformation biomarker, subsequently validated in two independent pretreatment cohorts. Taken together, our results provide a comprehensive view of the combined genomic and phenotypic evolution of malignant cells during transformation and shifting crosstalk between malignant cells and the TME.
滤泡性淋巴瘤(FL)向侵袭性形式的组织学转化与不良预后相关。这种演变的表型后果及其对肿瘤微环境(TME)的影响尚不清楚。我们对 11 对转化前后患者样本进行了单细胞全基因组测序(scWGS)和转录组测序(scWTS),并对未转化患者的其他样本进行了 scWTS。我们的分析揭示了单细胞分辨率下转化的进化动态,突出了 TME 景观的变化,出现了免疫细胞衰竭的特征,与恶性 B 表型的转变在调控生态系统中共同进化。scWGS 和 scWTS 的整合确定了在克隆肿瘤进化过程中上调的恶性细胞途径。通过多色免疫荧光,我们将这些发现转化为基于 TME 的转化生物标志物,并在两个独立的预处理队列中进行了验证。总之,我们的研究结果提供了恶性细胞在转化过程中以及恶性细胞与 TME 之间相互作用的综合基因组和表型演变的全面视图。