重编程
转录组
肿瘤微环境
癌症研究
肝癌
肿瘤细胞
生物
癌症
癌细胞
细胞
遗传学
肝细胞癌
基因表达
基因
作者
Lichun Ma,Maria O. Hernandez,Yongmei Zhao,Monika Mehta,Bao Tran,Michael C. Kelly,Zachary Rae,Jonathan M. Hernandez,Jeremy L. Davis,Sean P. Martin,David E. Kleiner,Stephen M. Hewitt,Kris Ylaya,Bradford J. Wood,Tim F. Greten,Xin Wei Wang
出处
期刊:Cancer Cell
[Elsevier]
日期:2019-10-01
卷期号:36 (4): 418-430.e6
被引量:429
标识
DOI:10.1016/j.ccell.2019.08.007
摘要
Cellular diversity in tumors is a key factor for therapeutic failures and lethal outcomes of solid malignancies. Here, we determined the single-cell transcriptomic landscape of liver cancer biospecimens from 19 patients. We found varying degrees of heterogeneity in malignant cells within and between tumors and diverse landscapes of tumor microenvironment (TME). Strikingly, tumors with higher transcriptomic diversity were associated with patient's worse overall survival. We found a link between hypoxia-dependent vascular endothelial growth factor expression in tumor diversity and TME polarization. Moreover, T cells from higher heterogeneous tumors showed lower cytolytic activities. Consistent results were found using bulk genomic and transcriptomic profiles of 765 liver tumors. Our results offer insight into the diverse ecosystem of liver cancer and its impact on patient prognosis.
科研通智能强力驱动
Strongly Powered by AbleSci AI