Brusatol Inhibits Proliferation, Migration, and Invasion of Nonsmall Cell Lung Cancer PC-9 Cells

被引:2
作者
Yang, Lu-Ming [1 ,2 ]
Zhou, Wen-Min [1 ,2 ]
Guo, Qiao-Ru [1 ,2 ]
Fan, Xin-Yue [1 ,2 ]
Huang, Dong-Yu [1 ,2 ]
Sun, Xiao-Fei [3 ]
Yuan, Jie [3 ]
Yu, Hua [4 ]
Chen, Hu-Biao [5 ]
Zhang, Jian-Ye [1 ,2 ]
机构
[1] Guangzhou Med Univ, Key Lab Mol Target & Clin Pharmacol, Sch Pharmaceut Sci, Guangzhou, Peoples R China
[2] Guangzhou Med Univ, Affiliated Hosp 5, Guangzhou, Peoples R China
[3] Xinjiang Second Med Coll, Dept Pharmaceut Sci, Karamay, Peoples R China
[4] Univ Macau, Inst Chinese Med Sci, State Key Lab Qual Res Chinese Med, Macau, Peoples R China
[5] Hong Kong Baptist Univ, Sch Chinese Med, Hong Kong, Peoples R China
基金
中国国家自然科学基金;
关键词
Antitumor; brusatol; lung cancer; migration; proliferation; BETA-CATENIN; BRUCEA-[!text type='JAVA']JAVA[!/text]NICA; COLORECTAL-CANCER; PATHWAY; STAT3; GROWTH; APOPTOSIS; MEDICINE; RESISTANCE; MECHANISM;
D O I
10.4103/2311-8571.353662
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Objective: The purpose of this study was to investigate the inhibitory effect of brusatol, a nigakilactone extracted from Brucea javanica, on lung cancer for development of therapeutic drugs. We explored the effects of brusatol on the proliferation, migration, and invasion of lung cancer PC-9 cells in vitro and analyzed the mechanisms involved. Materials and Methods: MTT assay was used to determine the effect of brusatol on the proliferative capacity of PC-9 and H1975 cells in vitro. The half-maximal inhibitory concentrations (IC50) were calculated and used as a reference for subsequent experiments. Variations in the number and size of tumor cell clusters were monitored by the colony formation assay as evidence for the effect of brusatol on cell proliferation. The effect of brusatol on the migration and invasion of PC-9 cells was evaluated using wound healing and transwell assays, respectively. Apoptosis in lung cancer cells was detected using the Annexin V-FITC/propidium iodide assay. The correlated anticancer mechanism was detected using Western blotting. Results: The IC50 values of brusatol acting on PC-9 and H1975 cells were 1.58 +/- 0.30 mu M and 31.34 +/- 2.72 mu M, respectively, according to the MTT experiment. In addition, brusatol suppressed PC-9 cell proliferation, migration, and invasion, as well as induced apoptosis, which may be related to the downregulation of epidermal growth factor receptor (EGFR), ss-catenin, Akt, and STAT3 expression. Conclusions: Brusatol showed potent anticancer activity against lung cancer PC-9 cells, inhibiting the proliferative capacity and metastatic potential of PC-9 cells. Its anticancer effect may be related to the downregulation of EGFR, ss-catenin, Akt, and STAT3.
引用
收藏
页码:454 / 460
页数:7
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