紫杉醇
克隆形成试验
癌症研究
蛋白激酶B
基因敲除
肺癌
活力测定
细胞生长
MTT法
细胞凋亡
细胞
医学
癌症
化学
肿瘤科
内科学
生物化学
作者
Farong Zang,Yuanquan Rao,Xinhai Zhu,Zhibing Wu,Hao Jiang
标识
DOI:10.1186/s10020-020-00152-8
摘要
Abstract Background The development of paclitaxel-resistance led to the tumor relapse and treatment failure of non-small cell lung cancer. Shikonin has been demonstrated to show anti-cancer activity in many cancer types. The present study aimed to investigate the anti-cancer activity of shikonin in paclitaxel-resistant non-small cell lung cancer treatment. Methods MTT, clonogenic assay, apoptotic cell death analysis, western blot, qRT-PCR, gene knockdown and overexpression, xenograft experiment, immunohistochemistry were performed. Results Shikonin decreased paclitaxel-resistant NSCLC cell viability and inhibited the growth of xenograft tumor. Shikonin induced apoptotic cell death of paclitaxel-resistant NSCLC cell lines and suppressed the level of NEAT1 and Akt signaling of paclitaxel-resistant NSCLC cell lines and xenograft tumors. Either low dose or high dose of shikonin considerably suppressed the cell growth and induced the cell apoptotic death in NEAT1 knockdown A549/PTX cells, and p-Akt expression was decreased. Conclusions Shikonin could be a promising candidate for paclitaxel-resistant NSCLC treatment.
科研通智能强力驱动
Strongly Powered by AbleSci AI