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Article Publish Status: FREE
Abstract Title:

Senescence Inducer Shikonin ROS-Dependently Suppressed Lung Cancer Progression.

Abstract Source:

Front Pharmacol. 2018 ;9:519. Epub 2018 May 23. PMID: 29875661

Abstract Author(s):

Hongming Zheng, Qiuju Huang, Suchao Huang, Xia Yang, Ting Zhu, Wensheng Wang, Haojia Wang, Shugui He, Liyan Ji, Ying Wang, Xiaoxiao Qi, Zhongqiu Liu, Linlin Lu

Article Affiliation:

Hongming Zheng

Abstract:

Lung adenocarcinoma (LAC), predominant subclassfication of lung cancer, leads high incidence and mortality annually worldwide. During the premalignant transition from lung adenomas to LAC, cellular senescence is regard as a critical physiological barrier against tumor progression. Nevertheless, the role of senescence in tumorigenesis is controversial and few senescence inducers are extensively determined. In this study, we used two classical cell lines A549 and H1299 and two NSCLC xenograft models on Balb/c-nude mice to reveal the pro-senescence effects of shikonin and the corresponding underlying mechanism in LAC. Shikonin, a pure compound isolated from the herbal medicine, remarkably stimulated cellular senescence including increased SAHF formation, enlarged cellular morphology, and induced SA-β-Gal positive staining. Further mechanism study revealed that the pro-senescence effect of shikonin was dependent on the increased intercellular ROS generation, which subsequently triggered DNA damage-p53/p21axis without activating oncogenes such as Ras and MEK-1. Meanwhile, Kdm2b, an H3K36me2-specific demethylase effectively suppressed ROS generation, was also notably suppressed by shikonin treatment. Moreover, shikonin at 10 mg/kg significantly inhibited tumor weights by 55.84% and 50.98% in A549 and H1299 xenograft model, respectively (<0.05) through activating cellular senescence. Our study suggested that shikonin, a ROS-dependent senescence inducer, could serve as a promising agent for further lung cancer treatment.

Study Type : Animal Study
Additional Links
Pharmacological Actions : Antiproliferative : CK(4773) : AC(3450)

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