An integrative drug repositioning framework discovered a potential therapeutic agent targeting COVID-19

Author:

Ge YiyueORCID,Tian TingzhongORCID,Huang Suling,Wan Fangping,Li Jingxin,Li Shuya,Wang Xiaoting,Yang Hui,Hong Lixiang,Wu Nian,Yuan Enming,Luo Yunan,Cheng Lili,Hu Chengliang,Lei Yipin,Shu Hantao,Feng Xiaolong,Jiang Ziyuan,Wu Yunfu,Chi Ying,Guo Xiling,Cui Lunbiao,Xiao Liang,Li Zeng,Yang Chunhao,Miao ZehongORCID,Chen LigongORCID,Li HaitaoORCID,Zeng Hainian,Zhao DanORCID,Zhu Fengcai,Shen Xiaokun,Zeng JianyangORCID

Abstract

AbstractThe global spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) requires an urgent need to find effective therapeutics for the treatment of coronavirus disease 2019 (COVID-19). In this study, we developed an integrative drug repositioning framework, which fully takes advantage of machine learning and statistical analysis approaches to systematically integrate and mine large-scale knowledge graph, literature and transcriptome data to discover the potential drug candidates against SARS-CoV-2. Our in silico screening followed by wet-lab validation indicated that a poly-ADP-ribose polymerase 1 (PARP1) inhibitor, CVL218, currently in Phase I clinical trial, may be repurposed to treat COVID-19. Our in vitro assays revealed that CVL218 can exhibit effective inhibitory activity against SARS-CoV-2 replication without obvious cytopathic effect. In addition, we showed that CVL218 can interact with the nucleocapsid (N) protein of SARS-CoV-2 and is able to suppress the LPS-induced production of several inflammatory cytokines that are highly relevant to the prevention of immunopathology induced by SARS-CoV-2 infection.

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Genetics

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