首页> 美国卫生研究院文献>BioMed Research International >Bu-Zhong-Yi-Qi Decoction, the Water Extract of Chinese Traditional Herbal Medicine, Enhances Cisplatin Cytotoxicity in A549/DDP Cells through Induction of Apoptosis and Autophagy
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Bu-Zhong-Yi-Qi Decoction, the Water Extract of Chinese Traditional Herbal Medicine, Enhances Cisplatin Cytotoxicity in A549/DDP Cells through Induction of Apoptosis and Autophagy

机译:中草药补水补中益气汤通过诱导细胞凋亡和自噬作用增强A549 / DDP细胞的顺铂细胞毒性

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摘要

Cisplatin is one of the most active cytotoxic agents for non-small cell lung cancer (NSCLC) treatment. However, the development of cisplatin resistance is common. Bu-Zhong-Yi-Qi decoction (BZYQD), a Chinese traditional herbal medicine, is widely used for the enhancement of antitumor effect in other medications. In this study, we evaluated the effect and drug-resistance reversal mechanism of BZYQD combined with cisplatin on cisplatin-resistant A549/DDP cells. Our results showed that BZYQD exhibited direct cytotoxic and chemosensitizing effects. Cotreatment with BZYQD and cisplatin induced intrinsic apoptotic pathways which were measured by condensed nuclear chromatin, Annexin V/PI apoptosis assay, and apoptosis related proteins expression. In addition, cotreatment with BZYQD and cisplatin also activated autophagy, as indicated by an increase in LC3 puncta, classical autophagosomes and/or autolysosomes, and an accumulation of LC3-II and ATG7 protein. Finally, cotreatment with BZYQD and cisplatin resulted in the generation of ROS and scavenging ROS by NAC almost completely suppressing cell death. These results suggest that cotreatment with BZYQD and cisplatin might reverse cisplatin resistance by inducing ROS accumulation, which activates apoptosis and autophagy by oxidative stress. The combination of BZYQD and cisplatin may represent a novel approach in treatment for NSCLC and thus offer a new target for chemotherapy.
机译:顺铂是用于非小细胞肺癌(NSCLC)治疗的最具活性的细胞毒性药物之一。但是,顺铂耐药性的发展是普遍的。补中益气汤(BZYQD)是一种中草药,被广泛用于增强其他药物的抗肿瘤作用。在这项研究中,我们评估了BZYQD联合顺铂对顺铂耐药A549 / DDP细胞的作用和耐药逆转机制。我们的结果表明BZYQD表现出直接的细胞毒性和化学增敏作用。与BZYQD和顺铂共同处理可诱导内在的凋亡途径,该途径可通过浓缩核染色质,膜联蛋白V / PI凋亡测定以及凋亡相关蛋白的表达来测定。此外,BZYQD和顺铂的共同治疗也可以激活自噬,如LC3点突,经典自噬体和/或自溶酶体的增加以及LC3-II和ATG7蛋白的积累所表明的。最后,与BZYQD和顺铂的共同处理导致ROS的生成和NAC清除ROS几乎完全抑制了细胞死亡。这些结果表明,与BZYQD和顺铂共同治疗可能通过诱导ROS积累而逆转顺铂耐药性,后者可通过氧化应激激活细胞凋亡和自噬。 BZYQD和顺铂的结合可能代表了一种治疗NSCLC的新方法,从而为化疗提供了新的靶点。

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