Gene interactions and pathways from curated databases and text-mining

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CDKN2A — RBBP7

Protein-Protein interactions - manually collected from original source literature:

Studies that report less than 10 interactions are marked with *

Text-mined interactions from Literome

Chung et al., Mol Ther 2003 (Arthritis, Rheumatoid...) : We found that the histone deacetylase (HDAC) inhibitors ( phenylbutyrate and trichostatin A ) causing histone hyperacetylation to modulate multiple gene expression not only induced the expression of p21 ( Cip1 ) and p16(INK4) in synovial cells but also inhibited the expression of tumor necrosis factor-alpha in affected tissues in adjuvant arthritis, an animal model of RA
Wang et al., Biochim Biophys Acta 2008 : Specifically, HDAC3 and HDAC4 inhibited the p16(INK4a) promoter activity
Zhou et al., Nucleic Acids Res 2009 : We also find that Lsh requires histone deacetylase (HDAC) activity to repress p16(INK4a) and treatment with trichostatin A (TSA) is sufficient to block the repressor effect of Lsh
Feng et al., FEBS J 2009 (Lung Neoplasms) : We also show that histone deacetylase (HDAC) 3 and HDAC4 inhibited p16(INK4a) promoter activity in a dose dependent manner