RNAactDrug: a comprehensive database of RNAs associated with drug sensitivity from multi-omics data

被引:38
作者
Dong, Qun [1 ]
Li, Feng [1 ]
Xu, Yanjun [1 ]
Xiao, Jing [1 ]
Xu, Yingqi [1 ]
Shang, Desi [1 ]
Zhang, Chunlong [1 ]
Yang, Haixiu [1 ]
Tian, Zihan [1 ]
Mi, Kai [1 ]
Li, Xia [1 ]
Zhang, Yunpeng [1 ]
机构
[1] Harbin Med Univ, Coll Bioinformat Sci & Technol, Harbin 150081, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
drug sensitivity; RNA5; integrative resource; multi-omics; RNAactDrug; RESISTANCE; MUTATIONS; HETEROGENEITY; ANNOTATION; MECHANISMS; THERAPY; GENES;
D O I
10.1093/bib/bbz142
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Drug sensitivity has always been at the core of individualized cancer chemotherapy. However, we have been overwhelmed by large-scale pharmacogenomic data in the era of next-generation sequencing technology, which makes it increasingly challenging for researchers, especially those without bioinformatic experience, to perform data integration, exploration and analysis. To bridge this gap, we developed RNAactDrug, a comprehensive database of RNA5 associated with drug sensitivity from multi-omics data, which allows users to explore drug sensitivity and RNA molecule associations directly. It provides association data between drug sensitivity and RNA molecules including mRNA5, long non-coding RNA5 (lncRNAs) and microRNAs (miRNAs) at four molecular levels (expression, copy number variation, mutation and methylation) from integrated analysis of three large-scale pharmacogenomic databases (GDSC, CellMiner and CCLE). RNAactDrug currently stores more than 4 924 200 associations of RNA molecules and drug sensitivity at four molecular levels covering more than 19 770 mRNA5, 11 119 lncRNAs, 438 miRNAs and 4155 drugs. A user-friendly interface enriched with various browsing sections augmented with advance search facility for querying the database is offered for users retrieving. RNAactDrug provides a comprehensive resource for RNA molecules acting in drug sensitivity, and it could be used to prioritize drug sensitivity-related RNA molecules, further promoting the identification of clinically actionable biomarkers in drug sensitivity and drug development more cost-efficiently by making this knowledge accessible to both basic researchers and clinical practitioners.
引用
收藏
页码:2167 / 2174
页数:8
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