Publication:
Curcuphenol possesses an unusual histone deacetylase enhancing activity that counters immune escape in metastatic tumours

dc.contributor.coauthorEllis, Samantha L. S.
dc.contributor.coauthorDada, Sarah
dc.contributor.coauthorNohara, Lilian L.
dc.contributor.coauthorSaranchova, Iryna
dc.contributor.coauthorMunro, Lonna
dc.contributor.coauthorPfeifer, Cheryl G.
dc.contributor.coauthorEyford, Brett A.
dc.contributor.coauthorMorova, Tunc
dc.contributor.coauthorWilliams, David E.
dc.contributor.coauthorCheng, Ping
dc.contributor.coauthorAndersen, Raymond J.
dc.contributor.coauthorJefferies, Wilfred A.
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorLack, Nathan Alan
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2025-01-19T10:32:53Z
dc.date.issued2023
dc.description.abstractCurcuphenol, a common component of the culinary spices, naturally found in marine invertebrates and plants, has been identified as a novel candidate for reversing immune escape by restoring expression of the antigen presentation machinery (APM) in invasive cancers, thereby resurrecting the immune recognition of metastatic tumours. Two synthetic curcuphenol analogues, were prepared by informed design that demonstrated consistent induction of APM expression in metastatic prostate and lung carcinoma cells. Both analogues were subsequently found to possess a previously undescribed histone deacetylase (HDAC)-enhancing activity. Remarkably, the H3K27ac ChIPseq analysis of curcuphenol-treated cells reveals that the induced epigenomic marks closely resemble the changes in genome-wide pattern observed with interferon-?, a cytokine instrumental for orchestrating innate and adaptive immunity. These observations link dietary components to modifying epigenetic programs that modulate gene expression guiding poised immunity.
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.openaccessgold, Green Published
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipWe would like to thank Kyung Bok Choi for many helpful discussions as well as Drs. Eliana Al Haddad and Giorgia Caspani for their editorial assistance.r This work was supported by an Industrial Partnered Collaborative Research grant from the Canadian Institutes of Health Research (CIHR; MOP-102698), in partnership with Pascal Biosciences, Inc. to WAJ; a grant from the Natural Sciences and Engineering Research Council (NSERC; RGPIN 869-13) to RJA; and TM was funded through a NSERC Bioinformatics CREATE Program co-hosted at the University of British Columbia and Simon Fraser University.
dc.description.volume14
dc.identifier.doi10.3389/fphar.2023.1119620
dc.identifier.eissn1663-9812
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-85168686015
dc.identifier.urihttps://doi.org/10.3389/fphar.2023.1119620
dc.identifier.urihttps://hdl.handle.net/20.500.14288/26494
dc.identifier.wos1053910500001
dc.keywordsEpigenetic modification
dc.keywordsAntigen processing machinery
dc.keywordsCurcuphenol
dc.keywordsMajor histocompatibility complex class I
dc.keywordsHistone deacetylase activity
dc.keywordsHDAC
dc.keywordsTumours
dc.keywordsDrug discovery
dc.language.isoeng
dc.publisherFrontiers Media Sa
dc.relation.grantnoThis work was supported by an Industrial Partnered Collaborative Research grant from the Canadian Institutes of Health Research (CIHR; MOP-102698), in partnership with Pascal Biosciences, Inc. to WAJ; a grant from the Natural Sciences and Engineering Resea [RGPIN 869-13]; Industrial Partnered Collaborative Research grant from the Canadian Institutes of Health Research (CIHR); Natural Sciences and Engineering Research Council (NSERC); NSERC Bioinformatics CREATE Program; [MOP-102698]
dc.relation.ispartofFrontiers in Pharmacology
dc.subjectPharmacology
dc.subjectPharmacy
dc.titleCurcuphenol possesses an unusual histone deacetylase enhancing activity that counters immune escape in metastatic tumours
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorLack, Nathan Alan
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit2School of Medicine
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