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Inhibition of super enhancer downregulates the expression of KLF5 in basal-like breast cancers

机译:Super Enhancer对基底乳腺癌中KLF5的表达下降

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The transcription factor KLF5 (Krüpple-like factor 5) is highly expressed in basal-like breast cancer (BLBC), which promotes cell proliferation, survival, migration and stemness, serving as a potential therapeutic target. In the current study, a super-enhancer (SE) was identified to be located downstream of the KLF5 gene in BLBC cell lines, HCC1806 and HCC1937. JQ-1, a BRD4 inhibitor, inhibits the expression and activity of KLF5 in both HCC1806 and HCC1937 cells in a time- and dose-dependent manner. Compound 870, an in-house BRD4 inhibitor, exhibited higher potency than JQ-1 to inhibit KLF5 and BLBC growth by arresting cells in G1 phase. Additionally, THZ1, a CDK7 inhibitor, also inhibits KLF5 and BLBC growth in a similar manner. Our findings suggested that KLF5 is regulated by SE, and modulation of SE could be an effective therapeutic strategy for treating BLBC.
机译:转录因子KLF5(Krüpple样系数5)在基础乳腺癌(BLBC)中高度表达,其促进了作为潜在治疗靶标的细胞增殖,存活,迁移和茎。在目前的研究中,鉴定了一种超强增强剂(SE)以位于短文细胞系中KLF5基因的下游,HCC1806和HCC1937。 JQ-1,BRD4抑制剂,以时间和剂量依赖性方式抑制KLF5在HCC1806和HCC1937细胞中的表达和活性。化合物870是内部BRD4抑制剂,通过在G1相中抑制细胞来抑制KLF5和BLBC生长的效力。另外,THZ1,CDK7抑制剂,也抑制KLF5和短文增长以类似的方式。我们的研究结果表明,KLF5由SE调节,SE的调节可能是治疗BLBC的有效治疗策略。

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