Jang Jun-Pil, Jung Hye Jin, Han Jang Mi, Jung Narae, Kim Yonghyo, Kwon Ho Jeong, Ko Sung-Kyun, Soung Nak-Kyun, Jang Jae-Hyuk, Ahn Jong Seog
Anticancer Agent Research Center, Korea Research Institute of Bioscience and Biotechnology, Cheongju, Republic of Korea.
Deparment of BT-Convergent Pharmaceutical Engineering, Sun Moon University, Chungnam, Republic of Korea.
PLoS One. 2017 Sep 26;12(9):e0184339. doi: 10.1371/journal.pone.0184339. eCollection 2017.
In the course of searching for angiogenesis inhibitors from microorganisms, two cyclic peptides, PF1171A (1) and PF1171C (2) were isolated from the soil fungus Penicillium sp. FN070315. In the present study, we investigated the antiangiogenic efficacy and associated mechanisms of 1 and 2 in vitro using human umbilical vein endothelial cells (HUVECs). Compounds 1 and 2 inhibited the proliferation of HUVECs at concentrations not exhibiting cytotoxicity. Moreover, 1 and 2 significantly suppressed vascular endothelial growth factor (VEGF)-induced migration, invasion, proliferation and tube formation of HUVECs as well as neovascularization of the chorioallantoic membrane in developing chick embryos. We also identified an association between the antiangiogenic activity of 1 and 2 and the downregulation of both the phosphorylation of VEGF receptor 2 and the expression of hypoxia inducible factor-1α at the protein level. Taken together, these results further suggest that compounds 1 and 2 will be promising angiogenesis inhibitors.
在从微生物中寻找血管生成抑制剂的过程中,从土壤真菌青霉菌FN070315中分离出了两种环肽,PF1171A(1)和PF1171C(2)。在本研究中,我们使用人脐静脉内皮细胞(HUVECs)在体外研究了1和2的抗血管生成功效及相关机制。化合物1和2在不表现出细胞毒性的浓度下抑制了HUVECs的增殖。此外,1和2显著抑制了血管内皮生长因子(VEGF)诱导的HUVECs迁移、侵袭、增殖和管形成,以及发育中的鸡胚尿囊绒毛膜的新血管形成。我们还确定了1和2的抗血管生成活性与VEGF受体2磷酸化和缺氧诱导因子-1α蛋白水平表达下调之间的关联。综上所述,这些结果进一步表明化合物1和2将是有前景的血管生成抑制剂。