Yang Runlei, Dong Qian, Xu Huibin, Gao XueHui, Zhao Ziyue, Qin Jianchun, Chen Chuan, Luo Duqiang
College of Life Science, Institute of Life Science and Green Development, Hebei University, Baoding, Hebei 071002, China.
College of Plant Science, Jilin University, Changchun, Jilin 130062, China.
ACS Omega. 2020 Sep 29;5(40):25927-25935. doi: 10.1021/acsomega.0c03315. eCollection 2020 Oct 13.
Phomoxanthone A and B (PXA and PXB) are xanthone dimers and isolated from the endophytic fungus sp. By254. The results demonstrated that PXB and PXA are noncompetitive inhibitors of SHP2 and PTP1B and competitive inhibitors of SHP1. Molecular docking studies showed that PXB and PXA interact with conserved domains of protein tyrosine phosphatases such as the β5-β6 loop, WPD loop, P loop, and Q loop. PXA and PXB could significantly inhibit the cell proliferation in MCF7 cells. Our results indicated that these two compounds do not efficiently inhibit PTP1B and SHP2 activity. RNA sequencing showed that PXA and PXB may inhibit SHP1 activity in MCF7 cells leading to the upregulation of inflammatory factors. In addition to PTP inhibition, PXA and PXB are multitarget compounds to inhibit the proliferation of tumor cells. In conclusion, both compounds show inhibition of cancer cells and a certain degree of inflammatory stimulation, which make them promising for tumor immunotherapy.
异戊二烯氧杂蒽酮A和B(PXA和PXB)是氧杂蒽酮二聚体,从内生真菌sp. By254中分离得到。结果表明,PXB和PXA是SHP2和PTP1B的非竞争性抑制剂,是SHP1的竞争性抑制剂。分子对接研究表明,PXB和PXA与蛋白质酪氨酸磷酸酶的保守结构域相互作用,如β5-β6环、WPD环、P环和Q环。PXA和PXB可显著抑制MCF7细胞的增殖。我们的结果表明,这两种化合物不能有效抑制PTP1B和SHP2的活性。RNA测序表明,PXA和PXB可能抑制MCF7细胞中SHP1的活性,导致炎症因子上调。除了抑制PTP外,PXA和PXB还是抑制肿瘤细胞增殖的多靶点化合物。总之,这两种化合物均显示出对癌细胞的抑制作用和一定程度的炎症刺激作用,这使其在肿瘤免疫治疗方面具有潜力。