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lncRNA MALAT1 binds chromatin remodeling subunit BRG1 to epigenetically promote inflammation-related hepatocellular carcinoma progression
Published in OncoImmunology, 2019
Mingyan Huang, Huamin Wang, Xiang Hu, Xuetao Cao
Continuing advances in transcriptomics revealed that long non-coding RNAs (lncRNAs) are one of the most important mediators in regulating differentiation and developmental processes and pathological responses. Abnormal expressions of lncRNAs like MALAT1, PCAT7, PVT1, and HOTAIR have been demonstrated to play important roles in tumorigenesis and tumor progression.18,19 LncRNAs can regulate gene expression at different levels, such as chromatin modification, transcription and post-transcriptional processing. Xist (X inactive specific transcript), the first identified lncRNA, recruits the polycomb complex to the X chromosome and then trimethylates lysine 27 residue of histone H3 to induce heterochromatin formation, finally rendering the silence of X chromosome.20 LncRNA NRON can bind to the transcription factor NFAT (nuclear factor of activated T cells) and impede nuclear accumulation of NFAT to inhibit downstream reactions.21