癌症干细胞
生物
肿瘤微环境
干细胞
癌变
间质细胞
癌症研究
重编程
癌症
肿瘤进展
癌细胞
转录组
细胞
细胞生物学
遗传学
基因表达
肿瘤细胞
基因
作者
Jihye L. Golino,Jing Bian,Xin Wang,Jianyang Fu,Xiao Bin Zhu,Julie Yeo,Michael C. Kelly,Freddy E. Escorcia,Maggie Cam,Changqing Xie
标识
DOI:10.3389/fcell.2023.1250215
摘要
Cholangiocarcinoma is a malignancy of the bile ducts that is driven by activities of cancer stem-like cells and characterized by a heterogeneous tumor microenvironment. To better understand the transcriptional profiles of cancer stem-like cells and dynamics in the tumor microenvironment during the progression of cholangiocarcinoma, we performed single-cell RNA analysis on cells collected from three different timepoints of tumorigenesis in a YAP/AKT mouse model. Bulk RNA sequencing data from TCGA (The Cancer Genome Atlas program) and ICGC cohorts were used to verify and support the finding. In vitro and in vivo experiments were performed to assess the stemness of cancer stem-like cells. We identified Tm4sf1high malignant cells as cancer stem-like cells. Across timepoints of cholangiocarcinoma formation in YAP/AKT mice, we found dynamic change in cancer stem-like cell/stromal/immune cell composition. Nevertheless, the dynamic interaction among cancer stem-like cells, immune cells, and stromal cells at different timepoints was elaborated. Collectively, these data serve as a useful resource for better understanding cancer stem-like cell and malignant cell heterogeneity, stromal cell remodeling, and immune cell reprogramming. It also sheds new light on transcriptomic dynamics during cholangiocarcinoma progression at single-cell resolution.
科研通智能强力驱动
Strongly Powered by AbleSci AI