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通过小分子阻断缺氧诱导因子-1α-p300 相互作用抑制 VEGF 转录。

Inhibition of VEGF transcription through blockade of the hypoxia inducible factor-1α-p300 interaction by a small molecule.

机构信息

Center for Theragnosis, Biomedical Research Institute, Korea Institute of Science and Technology, Hwarangno 14-gil, Seongbuk-gu, Seoul 136-791, Republic of Korea.

出版信息

Bioorg Med Chem Lett. 2012 Aug 15;22(16):5249-52. doi: 10.1016/j.bmcl.2012.06.054. Epub 2012 Jun 23.

Abstract

Vascular endothelial growth factor (VEGF) plays a pro-angiogenic role in tumor progression. Stabilization of a key regulator termed the hypoxia inducible factor (HIF)-1α under oxygen deficient environment around tumor is known to elicit expression of VEGF through binding to p300. Thus, inhibition of the HIF-1α-p300 interaction would lead to down-regulation of VEGF expression, thereby providing potential cancer therapeutics. Here, we have screened a chemical library against the interaction of the HIF-1α-derived peptide with p300 employing a fluorescence polarization-based assay. We have identified a compound as the most prominent inhibitor against the protein-protein interaction. Further, we have observed suppression of the mRNA level of VEGF upon treatment of HeLa cells with the compound, demonstrating its inhibitory effect at the cellular level.

摘要

血管内皮生长因子 (VEGF) 在肿瘤进展中发挥促血管生成作用。在肿瘤周围缺氧环境下,关键调节因子缺氧诱导因子 (HIF)-1α 的稳定被认为通过与 p300 结合来引发 VEGF 的表达。因此,抑制 HIF-1α-p300 相互作用会导致 VEGF 表达下调,从而为癌症治疗提供潜在靶点。在这里,我们使用基于荧光偏振的测定法筛选了针对 HIF-1α 衍生肽与 p300 相互作用的化学文库。我们已经确定了一种化合物作为针对蛋白质-蛋白质相互作用的最显著抑制剂。此外,我们观察到在用该化合物处理 HeLa 细胞后 VEGF 的 mRNA 水平受到抑制,证明了其在细胞水平的抑制作用。

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