阿帕蒂尼
体内
癌症研究
细胞凋亡
药理学
齐墩果酸
细胞生长
污渍
化学
癌症
医学
生物
病理
生物化学
内科学
生物技术
基因
替代医学
作者
Faisal Raza,Jing Ren,Jiaqin Yan,Hajra Zafar,Haopeng Wan,Xue Chen,Qingrong Cui,Haiyang Li,Xiangqi Wang
出处
期刊:Recent Patents on Anti-cancer Drug Discovery
[Bentham Science]
日期:2024-05-01
卷期号:19 (2): 199-208
标识
DOI:10.2174/1574892818666230417093208
摘要
As a pentacyclic triterpenoid, OA (oleanolic acid) has exhibited antiinflammatory, immunomodulatory and antitumor effects. VEGFR-2 (vascular endothelial cells receptor-2) tyrosine kinase activity could be inhibited by apatinib, a small-molecule antiangiogenic agent.Thus, this study sought to investigate the mechanism underlying the synergistic antitumor activity of combined OA and apatinib patent.Through CCK8 (Cell counting kit 8 assay), flow cytometric and western blotting techniques, we conducted in vitro studies on apatinib and OA effects on cell proliferation and apoptosis in H22 cell line. H22 tumor-burdened mice model was established in vivo, while the related signaling pathways were studied via pathological examination, western blotting and qPCR (quantitative polymerase chain reaction).Growth of H22 cells in vitro and in vivo could be inhibited effectively by apatinib and OA. Thus, OA repaired liver function and inhibited oxidative stress induced by apatinib.OA can treat apatinib induced liver injury in H22 Tumor-burdened mice by enhancing the suppresssive effect of apatinib on the growth of tumor.
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