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深度scSTAR:利用深度学习从单细胞RNA测序和空间转录组学数据中提取和增强表型相关特征。

Deep scSTAR: leveraging deep learning for the extraction and enhancement of phenotype-associated features from single-cell RNA sequencing and spatial transcriptomics data.

作者信息

Gao Lianchong, Liu Yujun, Zou Jiawei, Deng Fulan, Liu Zheqi, Zhang Zhen, Zhao Xinran, Chen Lei, Tong Henry H Y, Ji Yuan, Le Huangying, Zou Xin, Hao Jie

机构信息

Shanghai Center for Systems Biomedicine, Key Laboratory of Systems Biomedicine (Ministry of Education), Shanghai Jiao Tong University, 800# Dong Chuan Road, Minhang District, Shanghai 200240, China.

Department of Radiation Oncology, Fudan University Shanghai Cancer Center, Fudan University, Shanghai 200433, China.

出版信息

Brief Bioinform. 2025 May 1;26(3). doi: 10.1093/bib/bbaf160.

Abstract

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.

摘要

单细胞测序增进了我们对细胞异质性和疾病病理学的理解,为细胞行为和免疫机制提供了见解。然而,由于噪声、批次效应和无关的生物信号,提取有意义的表型相关特征具有挑战性。为了解决这个问题,我们引入了深度scSTAR(DscSTAR),这是一种基于深度学习的工具,旨在增强与表型相关的特征。DscSTAR在CD8+T细胞中识别出HSP+FKBP4+T细胞,这与非小细胞肺癌中的免疫功能障碍和免疫检查点阻断抗性有关。它还增强了肾细胞癌的空间转录组学分析,揭示了癌细胞、CD8+T细胞和肿瘤相关巨噬细胞之间的相互作用,这些相互作用可能促进免疫抑制并影响治疗结果。在肝细胞癌中,它突出了S100A12+中性粒细胞和癌症相关成纤维细胞在形成肿瘤免疫屏障以及可能导致免疫治疗抗性方面的作用。这些发现证明了DscSTAR对表型特异性信息进行建模和提取的能力,增进了我们对疾病机制和治疗抗性的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a74/12047704/90056105406d/bbaf160f1.jpg

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