Teroxirone motivates apoptotic death in tumorspheres of human lung cancer cells

被引:2
|
作者
Ni, Yu-Ling [1 ]
Hsieh, Chang-Heng [1 ]
Wang, Jing-Ping [1 ]
Fang, Kang [1 ]
机构
[1] Natl Taiwan Normal Univ, Sch Life Sci, 88 Ting Chow Rd,Sec 4, Taipei 116, Taiwan
关键词
Cancer stem cells; Teroxirone; Non-small cell lung cancer cells; Apoptosis; EPITHELIAL-MESENCHYMAL TRANSITION; STEM-CELLS; THERAPEUTIC TARGETS; GROWTH; P53; RESISTANCE; MICE;
D O I
10.1016/j.cbi.2018.06.011
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Therapy by targeting cancer stem cells (CSCs) is an eligible method to eradicate malignant human tumors. A synthetic triepoxide derivative, teroxirone, was reported effective against the growth of human lung cancer cells by injuring cellular mitochondria functions. And yet it remains unclear if the residual but malicious CSCs can be effectively dissipated following treatment. The current study further affirmed that teroxirone inhibited the propagation of CSCs as enriched from NSCLC cells by inducing p53 that lead to ultimate apoptosis. More evidence supported that the reduced stemness of the spheroids was associated with apoptotic death. The results consolidate the notion that teroxirone is a viable and effective therapeutic agent for eradicating human lung cancer.
引用
收藏
页码:137 / 143
页数:7
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