Evidence map›Paper›PMID 41160885›Full record

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.

Shurui Ma, Jianzhou Jiang, Ruiyu Zhang, Xinyi Ren, Dan Li, Xiangdong Li, Hong Mu, Peng Liu, Li Zuo, Tingting Zhao and 3 more

Abstract read
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Shurui MaSchool of Basic Medical Sciences, Anhui Medical University, Hefei 230032, China.
Jianzhou JiangState Key Laboratory of Medical Proteomics, National Center for Protein Sciences (Beijing), Academy of Military Medical Sciences, Beijing 102206, China.ORCID 0009-0002-1810-6260
Ruiyu ZhangDepartment of Radiation Oncology, Harbin Medical University Cancer Hospital, Harbin 150040, China.
Xinyi RenSchool of Basic Medical Sciences, Anhui Medical University, Hefei 230032, China.
Dan LiSchool of Basic Medical Sciences, Anhui Medical University, Hefei 230032, China.
Xiangdong LiState Key Laboratory of Medical Proteomics, National Center for Protein Sciences (Beijing), Academy of Military Medical Sciences, Beijing 102206, China.
Hong MuDepartment of Emergency, Beijing Tiantan Hospital, Capital Medical University, Beijing 100070, China.
Peng LiuState Key Laboratory of Medical Proteomics, National Center for Protein Sciences (Beijing), Academy of Military Medical Sciences, Beijing 102206, China.
Li ZuoSchool of Basic Medical Sciences, Anhui Medical University, Hefei 230032, China.
Tingting ZhaoSchool of Basic Medical Sciences, Anhui Medical University, Hefei 230032, China.
Anxin GuDepartment of Radiation Oncology, Harbin Medical University Cancer Hospital, Harbin 150040, China.
Dong LiSchool of Basic Medical Sciences, Anhui Medical University, Hefei 230032, China.ORCID 0000-0002-8680-0468
Zhongyang LiuSchool of Basic Medical Sciences, Anhui Medical University, Hefei 230032, China.ORCID 0000-0002-3371-2392

Funding

National Key Research and Development Program of China 2021YFA1301603National Key Research and Development Program of China 2023YFF1204600National Natural Science Foundation of China 32088101
6 · The paper itself

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.

Indexed as

Databases, GeneticDrug Resistance, NeoplasmNeoplasmsSingle-Cell AnalysisTranscriptomeAntineoplastic AgentsGene Expression ProfilingGene Expression Regulation, NeoplasticHumansSequence Analysis, RNAAntineoplastic Agents

Identifiers

PMID41160885
PMCPMC12807622

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.