Department of Biotechnology, Translational Research Center for Protein Function Control, College of Life Science & Biotechnology, Yonsei University, Seoul, Republic of Korea.
Biochem Biophys Res Commun. 2012 Jan 6;417(1):330-4. doi: 10.1016/j.bbrc.2011.11.109. Epub 2011 Dec 1.
Angiogenesis, the formation of new blood vessels from pre-existing ones, plays a critical role in normal and pathological phenotypes, including solid tumor growth and metastasis. Accordingly, the development of new anti-angiogenic agents is considered an efficient strategy for the treatment of cancer and other human diseases linked with angiogenesis. We have identified voacangine, isolated from Voacanga africana, as a novel anti-angiogenic agent. Voacangine inhibits the proliferation of HUVECs at an IC(50) of 18 μM with no cytotoxic effects. Voacangine significantly suppressed in vitro angiogenesis, such as VEGF-induced tube formation and chemoinvasion. Moreover, the compound inhibits in vivo angiogenesis in the chorioallantoic membrane at non-toxic doses. In addition, voacangine decreased the expression levels of hypoxia inducible factor-1α and its target gene, VEGF, in a dose-dependent manner. Taken together, these results suggest that the naturally occurring compound, voacangine, is a novel anti-angiogenic compound.
血管生成,即从预先存在的血管中形成新的血管,在正常和病理表型中起着关键作用,包括实体瘤的生长和转移。因此,开发新的抗血管生成药物被认为是治疗癌症和其他与血管生成相关的人类疾病的有效策略。我们已经鉴定出从非洲泡叶中分离得到的沃卡宁是一种新型的抗血管生成药物。沃卡宁在 18 μM 的 IC50 下抑制 HUVEC 的增殖,且没有细胞毒性作用。沃卡宁显著抑制体外血管生成,如 VEGF 诱导的管形成和趋化侵袭。此外,该化合物在非毒性剂量下抑制鸡胚尿囊膜中的体内血管生成。此外,沃卡宁以剂量依赖性方式降低缺氧诱导因子-1α及其靶基因 VEGF 的表达水平。综上所述,这些结果表明,天然存在的化合物沃卡宁是一种新型的抗血管生成化合物。