CDS-DB, an omnibus for patient-derived gene expression signatures induced by cancer treatment

Author:

Liu Zhongyang123ORCID,Chen Ruzhen1,Yang Lele12,Jiang Jianzhou13ORCID,Ma Shurui14,Chen Lanhui1,He Mengqi1,Mao Yichao3,Guo Congcong1,Kong Xiangya5,Zhang Xinlei5,Qi Yaning12,Liu Fengsong3,He Fuchu1,Li Dong1ORCID

Affiliation:

1. State Key Laboratory of Proteomics, Beijing Proteome Research Center, National Center for Protein Sciences (Beijing), Beijing Institute of Lifeomics , Beijing 102206 , China

2. College of Chemistry and Materials Science, Key Laboratory of Medicinal Chemistry and Molecular Diagnosis (Hebei University), Hebei University , Baoding 071002 , China

3. College of Life Sciences, Hebei University , Baoding 071002 , China

4. School of Basic Medicine, Anhui Medical University , Hefei 230032 , China

5. Beijing Cloudna Technology Company , Limited, Beijing 100029 , China

Abstract

Abstract Patient-derived gene expression signatures induced by cancer treatment, obtained from paired pre- and post-treatment clinical transcriptomes, can help reveal drug mechanisms of action (MOAs) in cancer patients and understand the molecular response mechanism of tumor sensitivity or resistance. Their integration and reuse may bring new insights. Paired pre- and post-treatment clinical transcriptomic data are rapidly accumulating. However, a lack of systematic collection makes data access, integration, and reuse challenging. We therefore present the Cancer Drug-induced gene expression Signature DataBase (CDS-DB). CDS-DB has collected 78 patient-derived, paired pre- and post-treatment transcriptomic source datasets with uniformly reprocessed expression profiles and manually curated metadata such as drug administration dosage, sampling time and location, and intrinsic drug response status. From these source datasets, 2012 patient-level gene perturbation signatures were obtained, covering 85 therapeutic regimens, 39 cancer subtypes and 3628 patient samples. Besides data browsing, download and search, CDS-DB also supports single signature analysis (including differential gene expression, functional enrichment, tumor microenvironment and correlation analyses), signature comparative analysis and signature connectivity analysis. This provides insights into drug MOA and its heterogeneity in patients, drug resistance mechanisms, drug repositioning and drug (combination) discovery, etc. CDS-DB is available at http://cdsdb.ncpsb.org.cn/.

Funder

National Natural Science Foundation of China

National Key Research and Development Program of China

Publisher

Oxford University Press (OUP)

Subject

Genetics

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