Abstract:
:For patients with COVID-19 caused by SARS-CoV-2, the damages to multiple organs have been clinically observed. Since most of current investigations for virus-host interaction are based on cell level, there is an urgent demand to probe tissue-specific features associated with SARS-CoV-2 infection. Based on collected proteomic datasets from human lung, colon, kidney, liver and heart, we constructed a virus-receptor network, a virus-interaction network and a virus-perturbation network. In the tissue-specific networks associated with virus-host crosstalk, both common and different key hubs are revealed in diverse tissues. Ubiquitous hubs in multiple tissues such as BRD4 and RIPK1 would be promising drug targets to rescue multi-organ injury and deal with inflammation. Certain tissue-unique hubs such as REEP5 might mediate specific olfactory dysfunction. The present analysis implies that SARS-CoV-2 could affect multi-targets in diverse host tissues, and the treatment of COVID-19 would be a complex task.
journal_name
J Mol Cell Bioljournal_title
Journal of molecular cell biologyauthors
Feng L,Yin YY,Liu CH,Xu KR,Li QR,Wu JR,Zeng Rdoi
10.1093/jmcb/mjaa033subject
Has Abstractpub_date
2020-07-08 00:00:00eissn
1674-2788issn
1759-4685pii
5869046pub_type
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