转录组
癌变
背景(考古学)
基因
生物
腺癌
电池类型
细胞
Notch信号通路
癌症研究
癌症
计算生物学
遗传学
食管癌
基因表达
古生物学
作者
Hongjin Wu,Juehua Yu,Ying Li,Qiang Hou,Rongjin Zhou,Ni Zhang,Jing Zhao,Mingfeng Jiang,Ziwei Li,Yuhui Hua,F. Charles Brunicardi,Shixiu Wu
出处
期刊:Cancer Letters
[Elsevier BV]
日期:2018-09-16
卷期号:438: 133-143
被引量:40
标识
DOI:10.1016/j.canlet.2018.09.017
摘要
Single-cell RNA sequencing and transcriptome analysis enable novel discovery and precise characterization of new cell types and states, which improves the understanding of the cellular context of tumorigenesis. Herein, we applied this powerful approach to analyze 368 single cells from three esophageal squamous cell carcinoma (ESCC) and two esophageal adenocarcinoma (EAC) tumors. Using inferred copy number variation analysis, we successfully distinguished carcinoma cells from heterogeneous cellular populations, identifying gene signatures and crucial cancer-related signaling pathways related to ESCC and EAC. In particular, we found that NOTCH signaling was exclusively activated in ESCC, but not in EAC. ESCC tumors with higher NOTCH activity were associated with significantly worse survival rates than those with lower NOTCH activity. Collectively, this study revealed that ESCC and EAC are distinct in terms of cellular transcriptome profiles, which leads to a wide range of intratumoral cellular heterogeneity. The findings suggest that different therapeutic strategies that target the differences between two types of esophageal cancers are required, guiding cancer-specific future drug development.
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