首页> 外文期刊>Oxidative Medicine and Cellular Longevity >Polypharmacological Profiles Underlying the Antitumor Property of Salvia miltiorrhiza Root (Danshen) Interfering with NOX-Dependent Neutrophil Extracellular Traps
【24h】

Polypharmacological Profiles Underlying the Antitumor Property of Salvia miltiorrhiza Root (Danshen) Interfering with NOX-Dependent Neutrophil Extracellular Traps

机译:丹参抗丹皮干扰NOX依赖的中性粒细胞外细胞陷阱的多药理学特征

获取原文
           

摘要

Danshen, the dried root of Salvia miltiorrhiza, one of the most investigated medicinal plants with well-defined phytochemical constituents, has shown prominent clinical outcomes for antioxidant, anti-inflammatory, and anticoagulant activities to attain vascular protection and additional benefits for cancer therapy. More recently, activation of neutrophil and excessive formation of neutrophil extracellular traps (NETs) have been observed in pathological conditions of metastatic cancers; thus, we hypothesized that suppression of NETs could account for an essential cellular event underlying Danshen-mediated reduction of the incidence of metastasis. Using an experimental pulmonary metastases model of red fluorescent protein- (RFP-) labeled gastric cancer cells in combination with macroscopic ex vivo live-imaging system, our data indicated that Danshen impaired the fluorescent intensity and quantity of metastatic nodules. Moreover, Danshen could prevent neutrophil trafficking to the metastatic sites with decreased plasma levels of neutrophil elastase (NE) and procoagulant potential featured by fibrinogen. We further established phorbol 12-myristate 13-acetate- (PMA-) induced NET formation of human neutrophils and screened representative active compounds derived from the hydrophilic and hydrophobic fractions of Danshen using qualitative and quantitative methods. As a result, we found that salvianolic acid B (Sal B) and 15,16-dihydrotanshinone I (DHT I) exhibited superior inhibitory activities on NET formation and significantly attenuated the levels of citrullinated histone H3 (citH3), a biomarker for NET formation. Multitarget biochemical assays demonstrated that Sal B and DHT I distinctly modulated the enzymatic cascade involved in NET formation. Sal B and DHT I could disrupt NET formation at the earlier stage by blocking the activities of myeloperoxidase (MPO) and NADPH oxidase (NOX), respectively. Lastly, combining treatment of Sal B and DHT I under subED50 doses displayed remarkable synergism effect on NET inhibition. Altogether, these data provide insight into how promiscuous compounds from herbal medicine can be effectively targeted NETs towards hematogenous metastasis of certain tumors.
机译:丹参是丹参的干燥根,丹参是研究最多的药用植物之一,具有明确的植物化学成分,在抗氧化剂,抗炎剂和抗凝剂的活性方面取得了显着的临床成果,可实现血管保护和癌症治疗的其他益处。最近,在转移性癌症的病理学状况中观察到嗜中性粒细胞的活化和嗜中性粒细胞胞外捕获物(NETs)的过度形成。因此,我们假设NET的抑制作用可能是丹参介导的转移发生率降低背后的重要细胞事件。使用带有红色荧光蛋白(RFP)标记的胃癌细胞的实验性肺转移模型与宏观离体活体成像系统相结合,我们的数据表明丹参会损害转移瘤的荧光强度和数量。此外,丹参可以通过降低血浆中性粒细胞弹性蛋白酶(NE)的水平和纤维蛋白原的促凝潜力来防止中性粒细胞向转移部位的转运。我们进一步建立了佛波醇12-肉豆蔻酸酯13-乙酸酯-(PMA-)诱导的人类嗜中性白血球净形成,并使用定性和定量方法筛选了丹参亲水级分和疏水级分衍生的代表性活性化合物。结果,我们发现丹酚酸B(Sal B)和15,16-二氢丹参酮I(DHT I)对NET形成表现出优异的抑制活性,并显着减弱了瓜氨酸化组蛋白H3(citH3)的水平,而NETH的生物标记物。多靶标生化分析表明,Sal B和DHT I明显调节了参与NET形成的酶促级联反应。 Sal B和DHT I可以通过分别阻断髓过氧化物酶(MPO)和NADPH氧化酶(NOX)的活性而在早期破坏NET的形成。最后,在subED50剂量下联合治疗Sal B和DHT I对NET抑制表现出显着的协同作用。总之,这些数据提供了对草药中混杂化合物如何有效地将NETs靶向某些肿瘤的血源性转移的见解。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号