scStateDynamics: deciphering the drug-responsive tumor cell state dynamics by modeling single-cell level expression changes

被引:0
作者
Guo, Wenbo [1 ]
Li, Xinqi [1 ]
Wang, Dongfang [2 ]
Yan, Nan [1 ]
Hu, Qifan [1 ]
Yang, Fan [3 ]
Zhang, Xuegong [1 ,4 ,5 ]
Yao, Jianhua [3 ]
Gu, Jin [1 ]
机构
[1] Tsinghua Univ, Dept Automat, BNRIST Bioinformat Div, MOE Key Lab Bioinformat, Beijing, Peoples R China
[2] Peking Univ, Biomed Pioneering Innovat Ctr BIOP, Beijing, Peoples R China
[3] Tencent, AI Lab, Shenzhen, Peoples R China
[4] Tsinghua Univ, Ctr Synthet & Syst Biol, Sch Life Sci, Beijing, Peoples R China
[5] Tsinghua Univ, Sch Med, Beijing, Peoples R China
来源
GENOME BIOLOGY | 2024年 / 25卷 / 01期
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Single-cell; Dynamics; Tumor; Drug response; CANCER; RESISTANCE; THERAPY; HETEROGENEITY;
D O I
10.1186/s13059-024-03436-y
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Understanding tumor cell heterogeneity and plasticity is crucial for overcoming drug resistance. Single-cell technologies enable analyzing cell states at a given condition, but catenating static cell snapshots to characterize dynamic drug responses remains challenging. Here, we propose scStateDynamics, an algorithm to infer tumor cell state dynamics and identify common drug effects by modeling single-cell level gene expression changes. Its reliability is validated on both simulated and lineage tracing data. Application to real tumor drug treatment datasets identifies more subtle cell subclusters with different drug responses beyond static transcriptome similarity and disentangles drug action mechanisms from the cell-level expression changes.
引用
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页数:25
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