School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China.
Guangdong Provincial Key Laboratory of New Drug Design and Evaluation, Guangzhou 510006, China.
Int J Mol Sci. 2021 Feb 8;22(4):1711. doi: 10.3390/ijms22041711.
Vascular endothelial growth factor (VEGF) is an angiogenic growth factor and plays a key role in tumor progression. The C-rich DNA sequence of promoter can form i-motif structure, which is a potential target for the development of novel anticancer agents. However, there is a limited number of chemotypes as the selective ligands of promoter i-motif, which leaves much room for development. Herein, we report the discovery of the natural oleanolic acid scaffold as a novel chemotype for the development of selective ligands of i-motif. A series of oleanolic acid derivatives as promoter i-motif ligands were synthesized. Subsequent evaluations showed that 3c could selectively bind to and stabilize promoter i-motif without significant binding to G-quadruplex, duplex DNA, and other oncogene i-motifs. Cell-based assays indicated that 3c could effectively downregulate gene transcription and expression in MCF-7 cells, inhibit tumor cells proliferation and migration, and induce cancer cells apoptosis. This work provides evidence of promoter i-motif as an anticancer target and will facilitate future efforts for the discovery of oleanolic acid-based selective ligands of promoter i-motif.
血管内皮生长因子 (VEGF) 是一种血管生成生长因子,在肿瘤进展中发挥关键作用。启动子的富含 C 的 DNA 序列可以形成 i -motif 结构,这是开发新型抗癌药物的潜在靶点。然而,作为启动子 i-motif 的选择性配体的化学型有限,这为开发留下了很大的空间。在此,我们报告了发现天然齐墩果酸支架作为开发启动子 i-motif 的选择性配体的新型化学型。合成了一系列作为启动子 i-motif 配体的齐墩果酸衍生物。随后的评估表明,3c 可以选择性地结合并稳定启动子 i-motif,而不会与 G-四链体、双链 DNA 和其他致癌基因 i-motif 发生明显结合。基于细胞的测定表明,3c 可以有效地下调 MCF-7 细胞中 基因的转录和表达,抑制肿瘤细胞的增殖和迁移,并诱导癌细胞凋亡。这项工作为启动子 i-motif 作为抗癌靶点提供了证据,并将有助于未来发现基于齐墩果酸的启动子 i-motif 选择性配体的努力。