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. 2020 Sep 14;2020:6095673. doi: 10.1155/2020/6095673

Table 2.

The chemical modulators of BRG1. This list summarizes the current research on the chemical modulators of BRG1. BRG1: Brahma-related gene-1; BRM: Brahma; CDK: cyclin-dependent kinase; ENT: entinostat; HO-1: heme oxygenase 1; H/R: hypoxia/reoxygenation; IsoPostC: isoflurane postconditioning; NAC: N-acetylcysteine; Nrf2: nuclear factor E2-related factor 2; PPC: propofol postconditioning; SPostC: sevoflurane postconditioning; STAT3: signal transducer and activator of transcription 3; SWI/SNF: switch/sucrose nonfermentable.

Modulators Known actions Ref.
Chemicals
 17β-estradiol 17β-estradiol antagonizes both the expression and activity of BRG1/BRM. [58]
 Adiponectin Adiponectin promotes HO-1 induction by simultaneously activating Nrf2 and BRG1 to reduce cardiac oxidative stress, improve cardiac hypertrophy, and prevent left ventricular dysfunction in diabetic patients. [39]
β-Adrenergic agonist In vitro stimulation of myocardial cells with angiotensin II or a β-adrenergic agonist results in increased BRG1 expression. [116]
 CDK inhibitors CDK9 inhibition dephosphorylates the SWI/SNF protein BRG1, which contributes to gene reactivation. [127]
 Darinaparsin Darinaparsin inhibits HO-1 transcription by causing BRG1 phosphorylation through G2/M cell cycle arrest. [33]
 ENT At the protein level, ENT reduces BRG1 protein abundance in Rh30 and U23674 cells, notably to an undetected level. [128]
 IsoPostC Emulsified IsoPostC protects the heart through BRG1/Nrf2/STAT3 signaling. [38]
 NAC The enhanced expression of BRG1 may be a new mechanism by which antioxidant NAC provides cardiac protection. [36]
 Oridonin Oridonin inhibits proliferation of Jurkat cells via the downregulation of BRG1. [129]
 PFI-3 PFI-3 is a highly potent, selective, and cell-permeable inhibitor for the BRG1/BRM. [130, 131]
 Phosphoaminoglycosides Preparations of phosphoaminoglycosides were identified as inhibitors of the in vitro activities of three SWI2/SNF2 family members. [132]
 PPC PPC provides protection to H/R-induced L02 cells by activating Nrf2 and BRG1. [41]
 Propofol Propofol alleviates oxidative stress in anoxia/reoxygenated hepatocytes by upregulating lncrna-TUG1/BRG1 pathway. [40]
 Rosiglitazone The expression of BRG1 was significantly increased in cardiac remodeling heart, and the change can be reversed by rosiglitazone. [124]
 SPostC SPostC prevents hypoxia-reoxygenation-induced cardiomyocyte damage and oxidative stress by activating Nrf2/BRG1/HO-1 signaling. [37]
 Tetrandrine Tetrandrine upregulated BRG1 expression in a dose- and time-dependent pattern in Hep-2 cells. [133]