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白杨素通过 AKT/HIF-1α 通路抑制 VEGF 表达、肿瘤血管生成和生长。

Acacetin inhibits VEGF expression, tumor angiogenesis and growth through AKT/HIF-1α pathway.

机构信息

Department of Pathology, Anatomy & Cell Biology, Thomas Jefferson University, Philadelphia, PA, USA.

出版信息

Biochem Biophys Res Commun. 2011 Sep 23;413(2):299-305. doi: 10.1016/j.bbrc.2011.08.091. Epub 2011 Aug 27.

Abstract

Acacetin (5,7-dihydroxy-4'-methoxyflavone) is a flavone compound, some of which have anti-cancerous effects. Vascular endothelial growth factor (VEGF) plays an important role in angiogenesis and tumor growth. In this study, we found that acacetin decreased the steady level of VEGF mRNA level and inhibited VEGF transcriptional activation. To further determine the potential mechanism of acacetin in inhibiting VEGF expression, we showed that acacetin inhibited HIF-1α expression and AKT activation. Over-expression of HIF-1α or AKT restored acacetin-decreasing VEGF transcriptional activation, indicating that AKT and HIF-1 are the essential downstream targets of acacetin for inhibiting VEGF expression in the cells. Moreover, acacetin significantly inhibited ovarian cancer cell-induced angiogenesis and tumor growth in vivo through inhibiting HIF-1α and VEGF expression. Acacetin did not change HIF-1α mRNA level, but inhibited HIF-1α protein level through increasing its degradation and decreasing its stability. These results indicate that acacetin may be a useful natural compound for ovarian cancer prevention and treatment.

摘要

白杨素(5,7-二羟基-4'-甲氧基黄酮)是一种黄酮类化合物,其中一些具有抗癌作用。血管内皮生长因子(VEGF)在血管生成和肿瘤生长中起着重要作用。在这项研究中,我们发现白杨素降低了 VEGF mRNA 水平的稳定水平,并抑制了 VEGF 的转录激活。为了进一步确定白杨素抑制 VEGF 表达的潜在机制,我们表明白杨素抑制 HIF-1α 的表达和 AKT 的激活。过表达 HIF-1α 或 AKT 恢复了白杨素降低的 VEGF 转录激活,表明 AKT 和 HIF-1 是白杨素抑制细胞中 VEGF 表达的必需下游靶标。此外,白杨素通过抑制 HIF-1α 和 VEGF 表达,显著抑制卵巢癌细胞诱导的血管生成和体内肿瘤生长。白杨素不改变 HIF-1α mRNA 水平,但通过增加其降解和降低其稳定性来抑制 HIF-1α 蛋白水平。这些结果表明,白杨素可能是预防和治疗卵巢癌的有用天然化合物。

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