PO.BCS02.05 · 生物信息与计算
利用Cflows揭示动态时间轨迹及其潜在的调控网络
Revealing dynamic temporal trajectories and underlying regulatory networks with Cflows
作者与单位 Authors & Affiliations
摘要 Abstract
中文摘要
尽管单细胞技术提供了肿瘤状态的快照,但构建连续轨迹并揭示因果性基因调控网络仍然是一项重大挑战。我们提出了Cflows,这是一个将神经ODE网络与Granger因果关系相结合的AI框架,能够从静态scRNA-seq数据中推断连续的细胞状态转变和基因调控相互作用。在一个捕捉30天内肿瘤球发育过程的全新5时间点数据集中,Cflows重建了通向肿瘤球形成或凋亡的两类轨迹。基于轨迹的起源细胞分析勾勒出一种以CD44 hi EPCAM+ CAV1+为特征的新型癌症干细胞谱型,并揭示了肿瘤球起始潜能在G2/M或S期细胞中呈细胞周期依赖性的富集。Cflows揭示了ESRRA是肿瘤形成基因调控网络的关键因果驱动因子。事实上,抑制ESRRA可显著降低体内肿瘤生长和转移。Cflows为从静态单细胞数据中揭示细胞转变和动态调控网络提供了一个强大的框架。
查看英文原文 English abstract
While single-cell technologies provide snapshots of tumor states, building continuous trajectories and uncovering causative gene regulatory networks remains a significant challenge. We present Cflows, an AI framework that combines neural ODE networks with Granger causality to infer continuous cell state transitions and gene regulatory interactions from static scRNA-seq data. In a new 5-time point dataset capturing tumorsphere development over 30 days, Cflows reconstructs two types of trajectories leading to tumorsphere formation or apoptosis. Trajectory-based cell-of-origin analysis delineated a novel cancer stem cell profile characterized by CD44 hi EPCAM + CAV1 + , and uncovered a cell cycle-dependent enrichment of tumorsphere-initiating potential in G2/M or S-phase cells. Cflows uncovers ESRRA as a crucial causal driver of the tumor-forming gene regulatory network. Indeed, ESRRA inhibition significantly reduces tumor growth and metastasis in vivo. Cflows offers a powerful framework for uncovering cellular transitions and dynamic regulatory networks from static single-cell data.
利益披露 Disclosure
S. Gupta, None..
X. Sun, None..
A. Tong, None..
M. Kuchroo, None..
D. Bhaskar, None..
C. Liu, None..
A. Venkat, None..
B. P. San Juan, None..
L. Rangel, None..
V. Rodriguez, None..
J. G. Lock, None.