首页> 美国卫生研究院文献>Cancers >DFIQ a Novel Quinoline Derivative Shows Anticancer Potential by Inducing Apoptosis and Autophagy in NSCLC Cell and In Vivo Zebrafish Xenograft Models
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DFIQ a Novel Quinoline Derivative Shows Anticancer Potential by Inducing Apoptosis and Autophagy in NSCLC Cell and In Vivo Zebrafish Xenograft Models

机译:DFIQ一种新型的喹啉衍​​生物通过诱导NSCLC细胞和体内斑马鱼异种移植模型中的细胞凋亡和自噬显示出抗癌潜力。

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摘要

Lung cancer is one of the deadliest cancers worldwide due to chemoresistance in patients with late-stage disease. Quinoline derivatives show biological activity against HIV, malaria, bacteriuria, and cancer. DFIQ is a novel synthetic quinoline derivative that induces cell death in both in vitro and in vivo zebrafish xenograft models. DFIQ induced cell death, including apoptosis, and the IC values were 4.16 and 2.31 μM at 24 and 48 h, respectively. DFIQ was also found to induce apoptotic protein cleavage and DNA damage, reduce cell cycle-associated protein expression, and disrupt reactive oxygen species (ROS) reduction, thus resulting in the accumulation of superoxide radicals. Autophagy is also a necessary process associated with chemotherapy-induced cell death. Lysosome accumulation and lysosome-associated membrane protein-2 (LAMP2) depletion were observed after DFIQ treatment, and cell death induction was restored upon treatment with the autophagy inhibitor 3-methyladenine (3-MA). Nevertheless, ROS production was found to be involved in DFIQ-induced autophagy activation and LAMP2 depletion. Our data provide the first evidence for developing DFIQ for clinical usage and show the regulatory mechanism by which DFIQ affects ROS, autophagy, and apoptosis.
机译:由于晚期疾病患者的化学耐药性,肺癌是全球最致命的癌症之一。喹啉衍生物显示出对HIV,疟疾,细菌尿和癌症的生物活性。 DFIQ是一种新颖的合成喹啉衍生物,可在体外和体内斑马鱼异种移植模型中诱导细胞死亡。 DFIQ诱导细胞死亡,包括细胞凋亡,在24 h和48 h时IC值分别为4.16和2.31μM。还发现DFIQ诱导凋亡蛋白裂解和DNA损伤,减少与细胞周期相关的蛋白表达,并破坏活性氧(ROS)的减少,从而导致超氧自由基的积累。自噬也是与化学疗法诱导的细胞死亡相关的必要过程。 DFIQ处理后,观察到溶酶体积累和溶酶体相关膜蛋白2(LAMP2)的消耗,并用自噬抑制剂3-甲基腺嘌呤(3-MA)处理后恢复了细胞死亡诱导。尽管如此,发现ROS的产生与DFIQ诱导的自噬激活和LAMP2耗竭有关。我们的数据为开发用于临床用途的DFIQ提供了第一个证据,并显示了DFIQ影响ROS,自噬和凋亡的调控机制。

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