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Gambogenic acid exerts anticancer effects in cisplatin-resistant non-small cell lung cancer cells
被引:16
|作者:
Shen, Daofu
[1
]
Wang, Yu
[2
]
Niu, Hongmei
[3
]
Liu, Chunying
[1
]
机构:
[1] Liaoning Univ Tradit Chinese Med, Coll Combine Tradit Chinese & Western Med, Dept Pathol, 79 Chongshan Eastern Rd, Shenyang 110847, Liaoning, Peoples R China
[2] Jinzhou Med Univ, Life Sci Inst, Jinzhou 121001, Liaoning, Peoples R China
[3] Jinzhou Med Univ, Dept Clin Lab, Affiliated Hosp 3, Jinzhou 121000, Liaoning, Peoples R China
基金:
中国国家自然科学基金;
关键词:
gambogenic acid;
A549;
Cis cells;
cell cycle arrest;
apoptosis;
RNA sequencing;
CYCLE ARREST;
P21;
EXPRESSION;
APOPTOSIS;
G1;
NANOPARTICLES;
TRANSCRIPTOME;
DEGRADATION;
INHIBITION;
MECHANISMS;
D O I:
10.3892/mmr.2020.10909
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Non-small cell lung cancer (NSCLC) is the most common type of lung cancer and the most common cause of mortality in patients with lung cancer. The efficacy of cisplatin-based chemotherapy in NSCLC is limited by drug resistance, therefore, the development of novel anticancer agents is required to overcome cisplatin resistance. The present study investigated the anticancer activity of gambogenic acid (GNA), derived from gamboge, in the cisplatin-resistant NSCLC cell line A549/Cis. GNA was revealed to have a potent inhibitory effect on cell growth in A549/Cis cells by blocking the cell cycle and inducing apoptosis. The investigation of the molecular mechanisms identified that GNA arrested the cell cycle at the G(1) phase through the downregulation of cyclin Ds, cyclin dependent kinase (CDK)4 and CDK6, and the upregulation of p53 and p21. In addition, GNA induced apoptosis by increasing the activation of caspase 3 and caspase 7, in addition to the cleavage of poly(ADP-ribose) polymerase. The results of the present study supported the potential application of GNA in cisplatin-resistant NSCLC.
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页码:1267 / 1275
页数:9
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