Kaicheng Zhou , Xingxiu Li , Yuan Yang , Dongyue Hou , Shuaiqi Wang , Hanbo Lin , Ruining Yin , Dianwen Ju , Xian Zeng , Shaofei Wang
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引用次数: 0
Abstract
The complexity of the tumor microenvironment (TME) makes cancer therapy challenging. Multi-targeting strategies often exhibit superior clinical benefits and dominate ongoing cancer clinical trials. However, existing multi-targeting strategies largely rely on empirical approaches. The rational design of target pairs (TPs) for multi-target cancer therapy development is a high priority but remains a significant challenge, which may benefit from single-cell omics technologies to decode the TME. However, there has been no thorough survey of clinically relevant cancer TPs and their characterization at the single-cell level. Here, we established the TargetPair database to address this gap by manually annotating TPs from drug combinations and multi-targeting drugs whose anti-tumor efficacy has been evaluated, and calculating their omics features at the single-cell level. The TargetPair database provides (1) 60 approved, 1,580 clinical-stage, and 7,424 experimental-stage TPs manually annotated from 3,470 clinical trials and 1,396 publications, and (2) the omics features of TPs (co-expression, distribution, expressed cell fractions, pathways, and single-cell gene networks) from manually curated scRNA-seq datasets derived from 55 pieces of literature (including 3,022,556 single cells, 13 cell types, 16 cancer types, and 588 patients). It can be freely accessed at https://www.targetpair.aiddlab.com via several search and browsing modes.
期刊介绍:
Journal of Molecular Biology (JMB) provides high quality, comprehensive and broad coverage in all areas of molecular biology. The journal publishes original scientific research papers that provide mechanistic and functional insights and report a significant advance to the field. The journal encourages the submission of multidisciplinary studies that use complementary experimental and computational approaches to address challenging biological questions.
Research areas include but are not limited to: Biomolecular interactions, signaling networks, systems biology; Cell cycle, cell growth, cell differentiation; Cell death, autophagy; Cell signaling and regulation; Chemical biology; Computational biology, in combination with experimental studies; DNA replication, repair, and recombination; Development, regenerative biology, mechanistic and functional studies of stem cells; Epigenetics, chromatin structure and function; Gene expression; Membrane processes, cell surface proteins and cell-cell interactions; Methodological advances, both experimental and theoretical, including databases; Microbiology, virology, and interactions with the host or environment; Microbiota mechanistic and functional studies; Nuclear organization; Post-translational modifications, proteomics; Processing and function of biologically important macromolecules and complexes; Molecular basis of disease; RNA processing, structure and functions of non-coding RNAs, transcription; Sorting, spatiotemporal organization, trafficking; Structural biology; Synthetic biology; Translation, protein folding, chaperones, protein degradation and quality control.