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Beyondcell:单细胞 RNA-seq 数据中靶向癌症治疗异质性。

Beyondcell: targeting cancer therapeutic heterogeneity in single-cell RNA-seq data.

机构信息

Bioinformatics Unit, Spanish National Cancer Research Centre (CNIO), Calle Melchor Fernandez Almagro, 3, 28029 , Madrid, Spain.

Laboratorio de Oncología Clínico-Traslacional, Unidad de Investigación en tumores Digestivos, Instituto de Investigación I+12, Hospital 12 de Octubre, Av. de Córdoba, 28041, Madrid, Spain.

出版信息

Genome Med. 2021 Dec 16;13(1):187. doi: 10.1186/s13073-021-01001-x.

DOI:10.1186/s13073-021-01001-x
PMID:34911571
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8675493/
Abstract

We present Beyondcell, a computational methodology for identifying tumour cell subpopulations with distinct drug responses in single-cell RNA-seq data and proposing cancer-specific treatments. Our method calculates an enrichment score in a collection of drug signatures, delineating therapeutic clusters (TCs) within cellular populations. Additionally, Beyondcell determines the therapeutic differences among cell populations and generates a prioritised sensitivity-based ranking in order to guide drug selection. We performed Beyondcell analysis in five single-cell datasets and demonstrated that TCs can be exploited to target malignant cells both in cancer cell lines and tumour patients. Beyondcell is available at: https://gitlab.com/bu_cnio/beyondcell .

摘要

我们提出了 Beyondcell,这是一种计算方法,用于在单细胞 RNA-seq 数据中识别具有不同药物反应的肿瘤细胞亚群,并提出癌症特异性治疗方法。我们的方法计算了药物特征集中的富集分数,描绘了细胞群体中的治疗簇(TCs)。此外,Beyondcell 确定了细胞群体之间的治疗差异,并生成了基于敏感性的优先级排序,以指导药物选择。我们在五个单细胞数据集上进行了 Beyondcell 分析,结果表明 TC 可用于靶向癌细胞系和肿瘤患者中的恶性细胞。Beyondcell 可在以下网址获得:https://gitlab.com/bu_cnio/beyondcell。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db4c/8675493/9177b0828aa7/13073_2021_1001_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db4c/8675493/f1c22d985039/13073_2021_1001_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db4c/8675493/87ba968adb6c/13073_2021_1001_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db4c/8675493/8dc83980b302/13073_2021_1001_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db4c/8675493/9177b0828aa7/13073_2021_1001_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db4c/8675493/f1c22d985039/13073_2021_1001_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db4c/8675493/87ba968adb6c/13073_2021_1001_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db4c/8675493/8dc83980b302/13073_2021_1001_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db4c/8675493/9177b0828aa7/13073_2021_1001_Fig4_HTML.jpg

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Identification of resistance pathways and therapeutic targets in relapsed multiple myeloma patients through single-cell sequencing.
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