Yi Qi Jie Du Decoction Inhibits Proliferation and Induces Apoptosis of Nasopharyngeal Carcinoma Stem Cells Through Mitochondrial Apoptosis Pathway

Objective: To assess the effects of Yi Qi Jie Du Decoction (YQJDD) on nasopharyngeal carcinoma stem cells (NPC-SCs) and investigate the underlying mechanism. Methods: NPC-SCs were collected in serum-free culture system and identified by the sphere formation assay. The effect of YQJDD on the prolifer...

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Bibliographic Details
Main Authors: Zhou Fang-Liang, He Lan, He Dan, Wang Xian-Wen, Shi Hong-Jian, He Ying-Chun, Cao De-Liang
Format: Article
Language:English
Published: KeAi Communications Co., Ltd. 2019-12-01
Series:Digital Chinese Medicine
Online Access:http://www.sciencedirect.com/science/article/pii/S2589377720300045
Description
Summary:Objective: To assess the effects of Yi Qi Jie Du Decoction (YQJDD) on nasopharyngeal carcinoma stem cells (NPC-SCs) and investigate the underlying mechanism. Methods: NPC-SCs were collected in serum-free culture system and identified by the sphere formation assay. The effect of YQJDD on the proliferation of NPC-SCs was detected using the Cell Counting Kit-8 assay. The change of mitochondrial membrane potential (ΔΨm) in NPC-SCs following treatment with YQJDD was investigated by JC-1 staining. The levels of apoptosis- associated proteins were examined using western blot analysis. Results: YQJDD significantly inhibited the proliferation of NPC-SCs in dose- and time-dependent manners. JC-1 staining revealed that YQJDD lowered the ΔΨm of NPC-SCs in a time- dependent manner. After treatment with YQJDD, the expression of cleaved caspase-3, -7 and -9, cleaved poly-ADP ribose polymerase, P21 and P53 were increased, while the expression of Survivin in NPC-SCs was decreased. However, the expression of cleaved caspase-8 remained nearly unchanged. Conclusions: YQJDD inhibits the growth and induces apoptosis of NPC-SCs via an intrinsic apoptosis pathway. Keywords: Nasopharyngeal carcinoma (NPC) Yi Qi Jie Du Decoction (YQJDD) Apoptosis, Cancer stem cells, Mitochondrial apoptosis pathway
ISSN:2589-3777