Artesunate exhibits synergistic anti-cancer effects with cisplatin on lung cancer A549 cells by inhibiting MAPK pathway

生物 肺癌 顺铂 癌症研究 MAPK/ERK通路 A549电池 青蒿琥酯 药理学 细胞生物学 细胞凋亡 免疫学 内科学 生物化学 遗传学 信号转导 化疗 医学 疟疾 恶性疟原虫
作者
Wen Li,Guangzhi Ma,Yunfu Deng,Qiang Wu,Zhu Wang,Qinghua Zhou
出处
期刊:Gene [Elsevier BV]
卷期号:766: 145134-145134 被引量:9
标识
DOI:10.1016/j.gene.2020.145134
摘要

Artesunate (ART) has been used extensively as anti-malarial drugs worldwide. Besides, it has also been reported to have anti-cancer activities. This study was aimed to explore the anti-cancer activity of ART in combination with cisplatin (CIS) on A549 cells.Cells were cultured with different concentrations of ART and/or CIS for 24, 48, or 72 h to test the anti-proliferative effects by CCK-8 assay. Colony formation assay and EdU staining were also performed. TUNEL staining was used to illustrate the morphologic changes. Cell cycle and apoptosis were determined by flow cytometry assay, and Western blot analysis was conducted to detect the expression of apoptosis- and proliferation-related proteins. Caspase activities were determined by colorimetric assay kit. Moreover, the synergistic effect of ART with CIS in A549 cell xenograft model was also determined.ART significantly inhibited cell proliferation in dose- and time-dependent manners. Collectively, the combination treatment remarkably decreased colony formation rates and increased the rates of TUNEL-positive cells compared with mono-treatment. Mechanistically, the combination treatment influenced the expression of Bcl-2, Bax, p-P53, Caspase-3/7, Caspase-9, CyclinB1, P34, P21, and synergistically regulated the activity of P38/JNK/ERK1/2 MAPK pathway. In mice A549 xenograft tumors, the combination strategy significantly increased the anti-cancer efficacy of ART and CIS alone, consistent with the in vitro observations.ART exhibited significant anti-tumor effect on A549 cells and this efficiency could be enhanced by combination with CIS.
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