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Small-molecule inhibitor targeting orphan nuclear receptor COUP-TFII for prostate cancer treatment

机译:小分子抑制剂靶向孤儿核受体COUP-TFII用于前列腺癌治疗

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The orphan nuclear receptor COUP-TFII is expressed at a low level in adult tissues, but its expression is increased and shown to promote progression of multiple diseases, including prostate cancer, heart failure, and muscular dystrophy. Suppression of COUP-TFII slows disease progression, making it an intriguing therapeutic target. Here, we identified a potent and specific COUP-TFII inhibitor through high-throughput screening. The inhibitor specifically suppressed COUP-TFII activity to regulate its target genes. Mechanistically, the inhibitor directly bound to the COUP-TFII ligand-binding domain and disrupted COUP-TFII interaction with transcription regulators, including FOXA1, thus repressing COUP-TFII activity on target gene regulation. Through blocking COUP-TFII’s oncogenic activity in prostate cancer, the inhibitor efficiently exerted a potent antitumor effect in xenograft mouse models and patient-derived xenograft models. Our study identified a potent and specific COUP-TFII inhibitor that may be useful for the treatment of prostate cancer and possibly other diseases.
机译:孤儿核受体Coup-TFII在成人组织中的低水平表达,但其表达增加并显示出促进多种疾病的进展,包括前列腺癌,心力衰竭和肌肉营养不良。抑制COUP-TFII缓慢疾病进展,使其成为一种有趣的治疗目标。在这里,我们通过高通量筛选鉴定了一种有效的Coup-TFII抑制剂。抑制剂特异性地抑制了Coup-TFII活性以调节其靶基因。机械地,抑制剂直接与Coup-TFII配体结合结构域结合并破坏了与转录调节剂的Coup-TFII相互作用,包括FOXA1,从而减轻靶基因调控的COUP-TFII活性。通过阻断COUP-TFII在前列腺癌中的致癌活性,抑制剂有效地施加了在异种移植小鼠模型和患者衍生的异种移植模型中的有效抗肿瘤作用。我们的研究确定了有效和特异性的Coup-TFII抑制剂,可用于治疗前列腺癌和可能的其他疾病。

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