TY - JOUR
T1 - Deep scSTAR
T2 - leveraging deep learning for the extraction and enhancement of phenotype-associated features from single-cell RNA sequencing and spatial transcriptomics data
AU - Gao, Lianchong
AU - Liu, Yujun
AU - Zou, Jiawei
AU - Deng, Fulan
AU - Liu, Zheqi
AU - Zhang, Zhen
AU - Zhao, Xinran
AU - Chen, Lei
AU - Tong, Henry H.Y.
AU - Ji, Yuan
AU - Le, Huangying
AU - Zou, Xin
AU - Hao, Jie
N1 - Publisher Copyright:
© The Author(s) 2025. Published by Oxford University Press.
PY - 2025/5/1
Y1 - 2025/5/1
N2 - Single-cell sequencing has advanced our understanding of cellular heterogeneity and disease pathology, offering insights into cellular behavior and immune mechanisms. However, extracting meaningful phenotype-related features is challenging due to noise, batch effects, and irrelevant biological signals. To address this, we introduce Deep scSTAR (DscSTAR), a deep learning-based tool designed to enhance phenotype-associated features. DscSTAR identified HSP+ FKBP4+ T cells in CD8+ T cells, which linked to immune dysfunction and resistance to immune checkpoint blockade in non-small cell lung cancer. It has also enhanced spatial transcriptomics analysis of renal cell carcinoma, revealing interactions between cancer cells, CD8+ T cells, and tumor-associated macrophages that may promote immune suppression and affect outcomes. In hepatocellular carcinoma, it highlighted the role of S100A12+ neutrophils and cancer-associated fibroblasts in forming tumor immune barriers and potentially contributing to immunotherapy resistance. These findings demonstrate DscSTAR’s capacity to model and extract phenotype-specific information, advancing our understanding of disease mechanisms and therapy resistance.
AB - Single-cell sequencing has advanced our understanding of cellular heterogeneity and disease pathology, offering insights into cellular behavior and immune mechanisms. However, extracting meaningful phenotype-related features is challenging due to noise, batch effects, and irrelevant biological signals. To address this, we introduce Deep scSTAR (DscSTAR), a deep learning-based tool designed to enhance phenotype-associated features. DscSTAR identified HSP+ FKBP4+ T cells in CD8+ T cells, which linked to immune dysfunction and resistance to immune checkpoint blockade in non-small cell lung cancer. It has also enhanced spatial transcriptomics analysis of renal cell carcinoma, revealing interactions between cancer cells, CD8+ T cells, and tumor-associated macrophages that may promote immune suppression and affect outcomes. In hepatocellular carcinoma, it highlighted the role of S100A12+ neutrophils and cancer-associated fibroblasts in forming tumor immune barriers and potentially contributing to immunotherapy resistance. These findings demonstrate DscSTAR’s capacity to model and extract phenotype-specific information, advancing our understanding of disease mechanisms and therapy resistance.
KW - deep learning
KW - phenotype-associated features
KW - scRNA-seq
KW - spatial transcriptomics
KW - tumor microenvironment
UR - https://www.scopus.com/pages/publications/105004461990
U2 - 10.1093/bib/bbaf160
DO - 10.1093/bib/bbaf160
M3 - Article
C2 - 40315434
AN - SCOPUS:105004461990
SN - 1467-5463
VL - 26
JO - Briefings in Bioinformatics
JF - Briefings in Bioinformatics
IS - 3
M1 - bbaf160
ER -