Matches in SemOpenAlex for { <https://semopenalex.org/work/W3154117126> ?p ?o ?g. }
- W3154117126 endingPage "5619" @default.
- W3154117126 startingPage "5605" @default.
- W3154117126 abstract "Increased expression of vascular cell adhesion molecule (VCAM)-1 on the activated arterial endothelial cell (EC) surface critically contributes to atherosclerosis which may in part be regulated by epigenetic mechanisms. This study investigated whether and how the clinically available histone deacetylases 1 and 2 (HDAC1/2) inhibitor drug Romidepsin epigenetically modulates VCAM-1 expression to suppress atherosclerosis. Methods: VCAM-1 expression was analyzed in primary human aortic EC (HAEC) treated with Romidepsin or transfected with HDAC1/2-targeting siRNA. Methylation of GATA6 promoter region was examined with methylation-specific PCR assay. Enrichment of STAT3 to GATA6 promoter was detected with chromatin immunoprecipitation. Lys685Arg mutation was constructed to block STAT3 acetylation. The potential therapeutic effect of Romidepsin on atherosclerosis was evaluated in Apoe-/- mice fed with a high-fat diet. Results: Romidepsin significantly attenuated TNFα-induced VCAM-1 expression on HAEC surface and monocyte adhesion through simultaneous inhibition of HDAC1/2. This downregulation of VCAM-1 was attributable to reduced expression of transcription factor GATA6. Romidepsin enhanced STAT3 acetylation and its binding to DNA methyltransferase 1 (DNMT1), leading to hypermethylation of the GATA6 promoter CpG-rich region at +140/+255. Blocking STAT3 acetylation at Lys685 disrupted DNMT1-STAT3 interaction, decreased GATA6 promoter methylation, and reversed the suppressive effects of HDAC1/2 inhibition on GATA6 and VCAM-1 expression. Finally, intraperitoneal administration of Romidepsin reduced diet-induced atherosclerotic lesion development in Apoe-/- mice, accompanied by a reduction in GATA6/VCAM-1 expression in the aorta. Conclusions: HDAC1/2 contributes to VCAM-1 expression and atherosclerosis by suppressing STAT3 acetylation-dependent GATA6 promoter methylation. These findings may provide a rationale for HDAC1/2-targeting therapy in atherosclerotic heart disease." @default.
- W3154117126 created "2021-04-26" @default.
- W3154117126 creator A5021374115 @default.
- W3154117126 creator A5026417335 @default.
- W3154117126 creator A5027767246 @default.
- W3154117126 creator A5031499311 @default.
- W3154117126 creator A5051347731 @default.
- W3154117126 creator A5055096305 @default.
- W3154117126 creator A5066913119 @default.
- W3154117126 creator A5085245305 @default.
- W3154117126 date "2021-01-01" @default.
- W3154117126 modified "2023-10-18" @default.
- W3154117126 title "HDAC1 and 2 regulate endothelial VCAM-1 expression and atherogenesis by suppressing methylation of the <i>GATA6</i> promoter" @default.
- W3154117126 cites W1490231232 @default.
- W3154117126 cites W1493846190 @default.
- W3154117126 cites W1506569093 @default.
- W3154117126 cites W1533942477 @default.
- W3154117126 cites W1627676039 @default.
- W3154117126 cites W1984988736 @default.
- W3154117126 cites W1987451500 @default.
- W3154117126 cites W1989421786 @default.
- W3154117126 cites W1990052798 @default.
- W3154117126 cites W2015230474 @default.
- W3154117126 cites W2023728729 @default.
- W3154117126 cites W2040491893 @default.
- W3154117126 cites W2046241907 @default.
- W3154117126 cites W2047490254 @default.
- W3154117126 cites W2057865864 @default.
- W3154117126 cites W2059127283 @default.
- W3154117126 cites W2071385669 @default.
- W3154117126 cites W2071889722 @default.
- W3154117126 cites W2072669480 @default.
- W3154117126 cites W2072990872 @default.
- W3154117126 cites W2073189570 @default.
- W3154117126 cites W2079003739 @default.
- W3154117126 cites W2083784041 @default.
- W3154117126 cites W2093155739 @default.
- W3154117126 cites W2094632858 @default.
- W3154117126 cites W2105164602 @default.
- W3154117126 cites W2107733280 @default.
- W3154117126 cites W2113056756 @default.
- W3154117126 cites W2113144329 @default.
- W3154117126 cites W2116704835 @default.
- W3154117126 cites W2120840165 @default.
- W3154117126 cites W2123032740 @default.
- W3154117126 cites W2126039851 @default.
- W3154117126 cites W2131950179 @default.
- W3154117126 cites W2140523553 @default.
- W3154117126 cites W2144993269 @default.
- W3154117126 cites W2146784178 @default.
- W3154117126 cites W2150182400 @default.
- W3154117126 cites W2159042861 @default.
- W3154117126 cites W2510126562 @default.
- W3154117126 cites W2518248979 @default.
- W3154117126 cites W2586435916 @default.
- W3154117126 cites W2607416752 @default.
- W3154117126 cites W2775506761 @default.
- W3154117126 cites W2790448250 @default.
- W3154117126 cites W2803090152 @default.
- W3154117126 cites W2896148208 @default.
- W3154117126 cites W2900856101 @default.
- W3154117126 cites W2909884354 @default.
- W3154117126 cites W2919761312 @default.
- W3154117126 cites W2970799943 @default.
- W3154117126 cites W2979113373 @default.
- W3154117126 doi "https://doi.org/10.7150/thno.55878" @default.
- W3154117126 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/8039941" @default.
- W3154117126 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/33859766" @default.
- W3154117126 hasPublicationYear "2021" @default.
- W3154117126 type Work @default.
- W3154117126 sameAs 3154117126 @default.
- W3154117126 citedByCount "14" @default.
- W3154117126 countsByYear W31541171262021 @default.
- W3154117126 countsByYear W31541171262022 @default.
- W3154117126 countsByYear W31541171262023 @default.
- W3154117126 crossrefType "journal-article" @default.
- W3154117126 hasAuthorship W3154117126A5021374115 @default.
- W3154117126 hasAuthorship W3154117126A5026417335 @default.
- W3154117126 hasAuthorship W3154117126A5027767246 @default.
- W3154117126 hasAuthorship W3154117126A5031499311 @default.
- W3154117126 hasAuthorship W3154117126A5051347731 @default.
- W3154117126 hasAuthorship W3154117126A5055096305 @default.
- W3154117126 hasAuthorship W3154117126A5066913119 @default.
- W3154117126 hasAuthorship W3154117126A5085245305 @default.
- W3154117126 hasBestOaLocation W31541171261 @default.
- W3154117126 hasConcept C104317684 @default.
- W3154117126 hasConcept C125449221 @default.
- W3154117126 hasConcept C150194340 @default.
- W3154117126 hasConcept C153911025 @default.
- W3154117126 hasConcept C185592680 @default.
- W3154117126 hasConcept C190727270 @default.
- W3154117126 hasConcept C2778305200 @default.
- W3154117126 hasConcept C2781462825 @default.
- W3154117126 hasConcept C33288867 @default.
- W3154117126 hasConcept C41091548 @default.
- W3154117126 hasConcept C502942594 @default.
- W3154117126 hasConcept C55493867 @default.
- W3154117126 hasConcept C64927066 @default.