ArticleNucleic acids research2026
scCT-DB, an omnibus for cancer patient-derived paired pre- and post-treatment single-cell transcriptomes to reveal drug perturbation and drug resistance mechanisms.
Article in Nucleic acids research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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Who cites it
3 citing papers in PubMed.
- DRIVE: a comprehensive resource deciphering drug-induced transcriptomic and splicing response in cancer cell.Neoplasia (New York, N.Y.) · 2026Article
- Multi-omics integration and clinical validation identify CKAP2 as a diagnostic biomarker for bladder cancer.World journal of surgical oncology · 2026Article
- The 2026 Nucleic Acids Research database issue and the online molecular biology database collection.Nucleic acids research · 2026Article
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13 authors.
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Abstract
Drug resistance continues to be a major challenge in cancer treatment. Understanding cellular and molecular dynamics after treatment is crucial for elucidating resistance mechanisms. Single-cell RNA sequencing (scRNA-seq) of paired pre- and post-treatment patient samples enables high-resolution exploration of such dynamics, but rapidly accumulated relevant data bring challenges for easy data access, integration, and reuse. Therefore, we present the Cancer Treatment-related Single-Cell transcriptome DataBase (scCT-DB, http://scctdb.ncpsb.org.cn). scCT-DB has comprehensively collected 266 patient-derived paired pre- and post-treatment scRNA-seq datasets processed by a uniform pipeline and with detailed and structured metadata, most of which simultaneously include information on primary/acquired drug response. scCT-DB includes 6.19 million cells from 1142 original patient samples, 27 major cancer types, 96 therapeutic regimens, and 102 drugs (involving chemotherapy, immunotherapy, hormone therapy, and targeted therapy). scCT-DB also provides 48 dataset pairs with opposite primary response groupings and 41 longitudinal datasets with ≥3 sampling timepoints. Besides data browsing, download, and search, scCT-DB also supports single-dataset analysis (including cell abundance, gene, cell state, and intercellular communication perturbation analyses), dataset comparative and re-combination analyses, providing insights into drug perturbation mechanisms and their heterogeneity in patients, drug resistance mechanisms, and discovery of biomarkers predictive of treatment response, etc.
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