Thrombospondin 4 (THBS4) activators represent a diverse group of chemicals that modulate THBS4 expression and activity. Indirect activators exert their influence through various cellular pathways, showcasing the complexity of THBS4 regulation. Lysophosphatidic acid (LPA) indirectly activates THBS4 by engaging G protein-coupled receptors and stimulating the Rho/ROCK and PI3K/Akt pathways. A769662, an AMP-activated protein kinase (AMPK) activator, indirectly activates THBS4 by relieving mTOR-mediated suppression and enhancing both transcription and translation processes. Epigenetic modulation by Trichostatin A, a histone deacetylase inhibitor, facilitates THBS4 transcription through histone acetylation.
Dibutyryl cAMP, a cyclic AMP analog, indirectly activates THBS4 by triggering cAMP/PKA signaling, enhancing CREB-mediated transcription, and impacting THBS4 stability. SB203580, a p38 MAPK inhibitor, disrupts the inhibitory feedback loop, indirectly activating THBS4. Rosiglitazone, a PPAR-γ agonist, influences THBS4 transcription and post-translational modifications through PPAR-γ activation. Wortmannin, a PI3K inhibitor, indirectly activates THBS4 by modulating PI3K/Akt signaling and affecting its stability. SP600125, a JNK inhibitor, disrupts the JNK-THBS4 feedback loop, indirectly activating THBS4. Bay 11-7082, an NF-κB inhibitor, indirectly activates THBS4 by modulating NF-κB signaling and disrupting the feedback loop. Forskolin, an adenylate cyclase activator, stimulates cAMP/PKA signaling, enhancing THBS4 transcription and stability. GSK690693, an Akt inhibitor, relieves Akt-mediated suppression, promoting THBS4 expression and stability. MG132, a proteasome inhibitor, indirectly activates THBS4 by preventing its degradation, highlighting the intricate interplay between proteasomal activity and THBS4 regulation. Collectively, these activators offer valuable insights into the intricate regulatory network governing THBS4 expression and function.
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