自噬
K562细胞
多重耐药
ATG5型
龙葵
程序性细胞死亡
体内
生物
细胞培养
药理学
PI3K/AKT/mTOR通路
小发夹RNA
癌细胞
癌症研究
白血病
抗药性
细胞生物学
信号转导
癌症
细胞凋亡
免疫学
微生物学
生物化学
基因敲除
生物技术
植物
遗传学
作者
Yi Wang,Siyu Wang,Jingwen Xu,Yihai Wang,Limin Xiang,Xiangjiu He
摘要
Abstract Multiple drug resistance (MDR) often occurs after prolonged chemotherapy, leading to refractory tumors and cancer recurrence. In this study, we demonstrated that the total steroidal saponins from Solanum nigrum L. (SN) had broad‐spectrum cytotoxic activity against various human leukemia cancer cell lines, especially in adriamycin (ADR)‐sensitive and resistant K562 cell lines. Moreover, SN could effectively inhibit the expression of ABC transporter in K562/ADR cells in vivo and in vitro. In vivo, by establishing K562/ADR xenograft tumor model, we demonstrated that SN might overcome drug resistance and inhibit the proliferation of tumors by regulating autophagy. In vitro, the increased LC3 puncta, the expression of LC3‐II and Beclin‐1, and the decreased expression of p62/SQSTM1 in SN‐treated K562/ADR and K562 cells demonstrated autophagy induced by SN. Moreover, using the autophagy inhibitors or transfecting the ATG5 shRNA, we confirmed that autophagy induced by SN was a key factor in overcoming MDR thereby promoting cell death in K562/ADR cells. More importantly, SN‐induced autophagy through the mTOR signaling pathway to overcome drug resistance and ultimately induced autophagy‐mediated cell death in K562/ADR cells. Taken together, our findings suggest that SN has the potential to treat multidrug‐resistant leukemia.
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