2021
DOI: 10.1016/j.jbc.2021.101070
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Suberoylanilide hydroxamic acid (SAHA) inhibits transforming growth factor-beta 2-induced increases in aqueous humor outflow resistance

Abstract: This is a PDF file of an article that has undergone enhancements after acceptance, such as the addition of a cover page and metadata, and formatting for readability, but it is not yet the definitive version of record. This version will undergo additional copyediting, typesetting and review before it is published in its final form, but we are providing this version to give early visibility of the article. Please note that, during the production process, errors may be discovered which could affect the content, a… Show more

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Cited by 10 publications
(16 citation statements)
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“…In addition to chromatin remodeling, HDACs affect non-histone proteins at specific sites, including tumor suppressors [31][32][33] and oncoproteins [34,35] involved in tumor signaling pathways, ultimately affecting cell fate [36]. HDACs deacetylate many groups of non-histone proteins including: transcription factors [37][38][39], cell adhesion proteins [40,41], cellular proteins [42], DNA repair proteins [43], cell signaling proteins [44,45], and viral proteins [46] (Figure 1C). However, HDACs role in tumorigenesis is controversial: either promoting cancer cell survival or causing cell death among different types of cancers [47][48][49][50].…”
Section: Epigenetic Basis Of Cancermentioning
confidence: 99%
“…In addition to chromatin remodeling, HDACs affect non-histone proteins at specific sites, including tumor suppressors [31][32][33] and oncoproteins [34,35] involved in tumor signaling pathways, ultimately affecting cell fate [36]. HDACs deacetylate many groups of non-histone proteins including: transcription factors [37][38][39], cell adhesion proteins [40,41], cellular proteins [42], DNA repair proteins [43], cell signaling proteins [44,45], and viral proteins [46] (Figure 1C). However, HDACs role in tumorigenesis is controversial: either promoting cancer cell survival or causing cell death among different types of cancers [47][48][49][50].…”
Section: Epigenetic Basis Of Cancermentioning
confidence: 99%
“…Cell proliferation was evaluated using the WST-8 assay (Cell Counting Kit-8, CCK-8; CK04, Dojindo, Kumamoto, Japan), as described previously 17 . SC cells were seeded in 96-well plates at 1 × 10 4 cells per well and incubated for 24 h. After serum starvation for 24 h, TGF-β2, Y-27632, BMP4 and SB203580 were added to the cells and incubated for 72 h. CCK-8, which is a detection reagent, was added and the absorbance at 450 nm was measured using a microplate reader (Multiskan FC, Thermo Fisher Scientific) after incubation for 2 h. Cell proliferation is presented as relative change compared to the control.…”
Section: Methodsmentioning
confidence: 99%
“…Fluorescent immunostaining of SC cells was performed as reported previously 17 , 47 . Phase-contrast images were acquired with an inverted microscope (IX71, Olympus, Tokyo, Japan) before fixation.…”
Section: Methodsmentioning
confidence: 99%
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