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Identification of Phomoxanthone A and B as Protein Tyrosine Phosphatase Inhibitors

机译:Phomox anthone A和B作为蛋白质酪氨酸磷酸酶抑制剂的鉴定

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摘要

Phomoxanthone A and B (PXA and PXB) are xanthone dimers and isolated from the endophytic fungus Phomopsis 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.
机译:Phomoxtonone A和B(PXA和PXB)是X原酮二聚体,并从内胚性真菌中分离出来 Phomopsis sp。到254。结果表明,PXB和PXA是SHP2和PTP1B的非竞争性抑制剂和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,例如β5-β6环,WPD环路,P环路和Q环。 PXA和PXB可显着抑制MCF7细胞中细胞增殖。我们的结果表明,这两种化合物没有有效地抑制PTP1B和SHP2活性。 RNA测序显示PXA和PXB可以抑制MCF7细胞中的SHP1活性,导致炎症因子的上调。除了PTP抑制作用,PXA和PXB是多靶案,以抑制肿瘤细胞的增殖。总之,两种化合物都显示出癌细胞的抑制和一定程度的炎症刺激,这使得它们对肿瘤免疫疗法有前途。

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