About: The Landscape of Human Cancer Proteins Targeted by SARS-CoV-2

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About: The Landscape of Human Cancer Proteins Targeted by SARS-CoV-2 Goto Sponge NotDistinct Permalink

An Entity of Type : schema:ScholarlyArticle, within Data Space : wasabi.inria.fr associated with source document(s)

Attributes	Values
type	Academic Article research paper schema:ScholarlyArticle
isDefinedBy	Covid-on-the-Web dataset
has title	The Landscape of Human Cancer Proteins Targeted by SARS-CoV-2
Creator	Gordon, David Krogan, Nevan Batra, Jyoti Bouhaddou, Mehdi Cakir, Merve Eckhardt, Manon Tutuncuoglu, Beril Org, Aacrjournals
Source	Medline; PMC
abstract	The mapping of SARS-CoV-2 human protein–protein interactions by Gordon and colleagues revealed druggable targets that are hijacked by the virus. Here, we highlight several oncogenic pathways identified at the host–virus interface of SARS-CoV-2 to enable cancer biologists to apply their knowledge for rapid drug repurposing to treat COVID-19, and help inform the response to potential long-term complications of the disease.
has issue date	2020-05-22(xsd:dateTime)
bibo:doi	10.1158/2159-8290.cd-20-0559
bibo:pmid	32444466
has license	no-cc
sha1sum (hex)	f018f29902aeb637122ec6e8b714df07a29a420e
schema:url	https://doi.org/10.1158/2159-8290.cd-20-0559
resource representing a document's title	The Landscape of Human Cancer Proteins Targeted by SARS-CoV-2
has PubMed Central identifier	PMC7357668
has PubMed identifier	32444466
schema:publication	Cancer Discov
resource representing a document's body	covid:f018f29902aeb637122ec6e8b714df07a29a420e#body_text
is schema:about of	named entity 'hijacked' named entity 'DRUG' named entity 'HELP' named entity 'APPLY' named entity 'KNOWLEDGE' named entity 'SARS-CoV-2' named entity 'Here' named entity 'potential' named entity 'Map' named entity 'drug repurposing' named entity 'virus' named entity 'mRNAs' named entity 'apoptosis' named entity 'Viruses' named entity 'highly conserved' named entity 'histone methyltransferase' named entity 'Vero E6' named entity 'phenotypes' named entity 'viral replication' named entity 'NUP98' named entity 'downregulation' named entity 'stress granules' named entity 'metabolic' named entity 'influenza virus' named entity 'electron transport chain' named entity 'tumorigenesis' named entity 'virus' named entity 'SARS-CoV-2' named entity 'viruses' named entity 'rapamycin' named entity 'COVID' named entity 'BRAF' named entity 'HSP90' named entity 'mass spectrometry' named entity 'hallmarks of cancer' named entity 'SARS-CoV' named entity 'nucleus' named entity 'MYC' named entity 'H3K36' named entity 'cancer treatment' named entity 'protein-protein interactions' named entity 'poliovirus' named entity 'BRD4' named entity 'fatty acid synthase' named entity 'University of California, San Francisco' named entity 'PTEN' named entity 'breast cancer' named entity 'CPI-0610' named entity 'interact' named entity 'DNA damage' named entity 'acute respiratory distress syndrome' named entity 'global pandemic' named entity 'Pevonedistat' named entity 'mutation' named entity 'cytokinesis' named entity 'cell survival' named entity 'DNA replication' named entity 'interact' named entity 'HIV' named entity 'mitotic spindle' named entity 'molecular mechanisms' named entity 'Mitochondrial metabolism' named entity 'Valproic acid' named entity 'IBV' named entity 'cofactor' named entity 'carcinogenesis' named entity 'protein' named entity 'viral infection' named entity 'public health' named entity 'RNA helicase' named entity 'reactive oxygen species' named entity 'metabolic' named entity 'avian coronavirus' named entity 'chemoinformatic'

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