4.8 Article

CancerResource: a comprehensive database of cancer-relevant proteins and compound interactions supported by experimental knowledge

期刊

NUCLEIC ACIDS RESEARCH
卷 39, 期 -, 页码 D960-D967

出版社

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkq910

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  1. International Research Training Group IRTG (Genomics and Systems Biology of Molecular Networks) Deutsche Krebshilfe
  2. Deutsche Forschungsgemeinschaft DFG
  3. Federal Ministry of Education and Research BMBF
  4. European Union EU

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During the development of methods for cancer diagnosis and treatment, a vast amount of information is generated. Novel cancer target proteins have been identified and many compounds that activate or inhibit cancer-relevant target genes have been developed. This knowledge is based on an immense number of experimentally validated compound-target interactions in the literature, and excerpts from literature text mining are spread over numerous data sources. Our own analysis shows that the overlap between important existing repositories such as Comparative Toxicogenomics Database (CTD), Therapeutic Target Database (TTD), Pharmacogenomics Knowledge Base (PharmGKB) and DrugBank as well as between our own literature mining for cancer-annotated entries is surprisingly small. In order to provide an easy overview of interaction data, it is essential to integrate this information into a single, comprehensive data repository. Here, we present CancerResource, a database that integrates cancer-relevant relationships of compounds and targets from (i) our own literature mining and (ii) external resources complemented with (iii) essential experimental and supporting information on genes and cellular effects. In order to facilitate an overview of existing and supporting information, a series of novel information connections have been established. CancerResource addresses the spectrum of research on compound-target interactions in natural sciences as well as in individualized medicine; CancerResource is available at: http://bioinformatics.charite.de/cancerresource/.

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