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丹参根抑制依赖 NOX 的中性粒细胞细胞外陷阱形成的抗肿瘤作用的多药理学特性。

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

机构信息

College of Medicine, Yangzhou University, Yangzhou, Jiangsu 225001, China.

The State Administration of Traditional Chinese Medicine Key Laboratory of Toxic Pathogens-Based Therapeutic Approaches of Gastric Cancer, Yangzhou University, Yangzhou, Jiangsu 225009, China.

出版信息

Oxid Med Cell Longev. 2018 Aug 19;2018:4908328. doi: 10.1155/2018/4908328. eCollection 2018.

Abstract

Danshen, the dried root of , 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 subED 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.

摘要

丹参, 作为最受研究的药用植物之一,其干燥根中含有明确的植物化学成分,已显示出抗氧化、抗炎和抗凝活性,从而达到血管保护作用,并为癌症治疗提供额外益处。最近,在转移性癌症的病理条件下观察到中性粒细胞的激活和中性粒细胞胞外诱捕网(NETs)的过度形成;因此,我们假设抑制 NETs 可能是丹参介导降低转移发生率的关键细胞事件。我们使用红色荧光蛋白(RFP)标记的胃癌细胞的实验性肺转移模型,结合宏观离体活体成像系统,数据表明丹参可减弱转移性结节的荧光强度和数量。此外,丹参可以阻止中性粒细胞向转移部位迁移,同时降低血浆中性粒细胞弹性蛋白酶(NE)和纤维蛋白原的促凝潜能。我们进一步建立了佛波醇 12-肉豆蔻酸 13-乙酸酯(PMA)诱导的人中性粒细胞 NET 形成,并使用定性和定量方法筛选丹参的亲水性和疏水性部分中代表性的活性化合物。结果发现,丹酚酸 B(Sal B)和 15,16-二氢丹参酮 I(DHT I)对 NET 形成具有优越的抑制活性,并显著降低 NET 形成的生物标志物瓜氨酸化组蛋白 H3(citH3)的水平。多靶标生化测定表明,Sal B 和 DHT I 分别通过阻断髓过氧化物酶(MPO)和 NADPH 氧化酶(NOX)的活性,显著调节 NET 形成的酶级联反应。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,在早期阶段破坏 NET 的形成。最后,在亚 ED 剂量下联合使用 Sal B 和 DHT I 治疗对 NET 抑制具有显著的协同作用。总的来说,这些数据为草药中的混杂化合物如何有效地靶向 NETs 以抑制某些肿瘤的血源性转移提供了深入了解。

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