Brd4 and HEXIM1: Multiple roles in P-TEFb regulation and cancer

Ruichuan Chen, Jasper H.N. Yik, Qiao Jing Lew, Sheng Hao Chao

    Research output: Contribution to journalReview articlepeer-review

    59 Scopus citations

    Abstract

    Bromodomain-containing protein 4 (Brd4) and hexamethylene bisacetamide (HMBA) inducible protein 1 (HEXIM1) are two opposing regulators of the positive transcription elongation factor b (P-TEFb), which is the master modulator of RNA polymerase II during transcriptional elongation. While Brd4 recruits P-TEFb to promoter-proximal chromatins to activate transcription, HEXIM1 sequesters P-TEFb into an inactive complex containing the 7SK small nuclear RNA. Besides regulating P-TEFb's transcriptional activity, recent evidence demonstrates that both Brd4 and HEXIM1 also play novel roles in cell cycle progression and tumorigenesis. Here we will discuss the current knowledge on Brd4 and HEXIM1 and their implication as novel therapeutic options against cancer.

    Original languageEnglish (US)
    Article number232870
    JournalBioMed Research International
    Volume2014
    DOIs
    StatePublished - 2014

    ASJC Scopus subject areas

    • General Biochemistry, Genetics and Molecular Biology
    • General Immunology and Microbiology

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