Differentially expressed genes of HepG2 cells treated with gecko polypeptide mixture

被引:12
作者
Duan, Yi-Meng [1 ]
Jin, Ying [1 ]
Guo, Meng-Li [1 ]
Duan, Leng-Xin [1 ]
Wang, Jian-Gang [1 ]
机构
[1] Henan Univ Sci & Technol, Dept Pharm, Med Coll, Luoyang 471023, Henan, Peoples R China
关键词
gecko; RNA-seq technology; hepatocellular carcinoma; reactive oxygen species; apoptosis; ENDOPLASMIC-RETICULUM STRESS; MEDIATED ER STRESS; HEPATOCELLULAR-CARCINOMA; INDUCED APOPTOSIS; CANCER CELLS; ROS; MECHANISM; ACTIVATION; CALCIUM; GROWTH;
D O I
10.7150/jca.26339
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Gecko (Gekko japonicus) extracts have been used in traditional Chinese medicine for many years. It has been proven that the gecko polypeptide mixture (GPM) extracted from gecko can inhibit the growth of multiple types of tumor cells. In order to investigate the possible anti-tumor molecular mechanisms of GPM, we used RNA-seq technology to identify the differentially expressed genes (DEGs) of human hepatocellular carcinoma (HCC) HepG2 cells treated with or without GPM. MTT assay was used to detect the viability of HepG2 cells. DAPI fluorescence staining was performed to observe morphological changes in the nuclei of HepG2 cells. Western blot analysis was applied to observe the expressions of apoptosis-related and endoplasmic reticulum stress (ERS)-related proteins in HepG2 cells. Flow cytometry assay was performed to detect the apoptosis and reactive oxygen species (ROS) in HepG2 cells. Our results showed that GPM inhibited HepG2 cells proliferation and induced the apoptosis of HepG2 cells. RNA-seq analysis suggested that the ER-nucleus signaling pathway involved in the anti-cancer molecular mechanism of GPM. Therefore, GPM may induce apoptosis in HepG2 cells via the ERs pathway.
引用
收藏
页码:2723 / 2733
页数:11
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