Department of Orthopedics, Xiangya Hospital, Central South University, PR China; Phase I Clinical Trial Center, Xiangya Hospital, Central South University, PR China.
School of Life Sciences, Central South University, PR China.
Bioorg Med Chem Lett. 2022 Jan 15;56:128486. doi: 10.1016/j.bmcl.2021.128486. Epub 2021 Dec 4.
A new biflavonoid, (2''S)-6''-methyl-2'',3''-dihydroochnaflavone (1), along with two known ochnaflavones (2, 3), four known amentoflavones (4-7) and two known robustaflavones (8, 9) were obtained from the 70% EtOH extract of Selaginella trichoclada. The chemical structures of isolated compounds were elucidated by extensive spectroscopic analyses. Overall, compounds 1-9 displayed moderate cytotoxic effects against human breast cancer MCF-7 cell lines. Among them, compounds 2 and 8 exhibited relatively strong cytotoxic effects against MCF-7 cells with an IC value of 7.7 and 6.9 μΜ, respectively. The results of RNA-sequencing and KEGG functional enrichment analysis showed that 8 could induce ferroptosis in MCF-7 cells by down-regulating the expression of ferroptosis-related genes including ACSL4, NOXO1, NOXA1, ACSL5, STEAP3, LPCAT3, ATG7 and TP53. Then 8 could inhibit the expression of ACSL4 proteins through molecule docking analysis, which showed a strong interaction of - 11.89 Kcal/mol binding energy. Those results indicate that 8 could be chemotherapy agents to fight drug resistance in breast cancer by down-regulating the expression level of ACSL4 proteins via ferroptosis, which needs to be further certified in vitro.
从卷柏的 70%乙醇提取物中分离得到一个新的双黄酮类化合物(2'S)-6'-甲基-2',3'-二氢奥卡黄酮(1),以及两个已知的奥卡黄酮(2,3),四个已知的穗花杉双黄酮(4-7)和两个已知的罗伯士塔黄酮(8,9)。通过广泛的光谱分析阐明了分离化合物的化学结构。总的来说,化合物 1-9 对人乳腺癌 MCF-7 细胞系表现出中等的细胞毒性作用。其中,化合物 2 和 8 对 MCF-7 细胞表现出相对较强的细胞毒性作用,IC 值分别为 7.7 和 6.9 μΜ。RNA-seq 和 KEGG 功能富集分析的结果表明,8 通过下调包括 ACSL4、NOXO1、NOXA1、ACSL5、STEAP3、LPCAT3、ATG7 和 TP53 在内的铁死亡相关基因的表达,诱导 MCF-7 细胞发生铁死亡。然后,通过分子对接分析发现 8 可以抑制 ACSL4 蛋白的表达,其结合能为-11.89 Kcal/mol。这些结果表明,8 可以通过铁死亡下调 ACSL4 蛋白的表达水平,成为治疗乳腺癌耐药的化疗药物,这需要在体外进一步验证。