RETRACTED: Neferine hinders choriocarcinoma cell proliferation, migration and invasion through repression of long noncoding RNA-CHRF (Retracted article. See vol. 48, pg. 998, 2020)

被引:6
|
作者
Wang, Gang [1 ]
Wang, Ping [2 ]
Yan, Xiaojun [2 ]
Liu, Jing [2 ]
机构
[1] Shandong Univ, Shandong Prov ENT Hosp, Dept Gynecol, Jinan, Shandong, Peoples R China
[2] Shandong First Med Univ, Laigang Hosp, Dept Obstet, 68 Xinxing Rd, Jinan 271100, Shandong, Peoples R China
关键词
Choriocarcinoma; neferine; cardiac hypertrophy related factor (CHRF); PI3K; AKT; mTOR; ERK1; 2; LOTUS SEED EMBRYO; GASTRIC-CANCER; APOPTOSIS; GROWTH; CHEMOTHERAPY; METASTASIS; TUMOR; ROS;
D O I
10.1080/21691401.2019.1671429
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The comprehensive pathological peculiarities of Neferine (NEF) have been testified in disparate diseases. But, the functions of NEF in choriocarcinoma progression remain unexplored. The research endeavoured to uncover the anti-tumour action of NEF in choriocarcinoma cells. NEF at diverse doses was employed to dispose JEG-3 and HTR-8 cells, and cell viability assessment adopted CCK-8 assay. After 60 ?g/mL NEF management, BrdU-positive cells, apoptosis, migration, invasion and correlative factors were assessed. CHRF expression in choriocarcinoma tumour and choriocarcinoma cell lines was estimated via RT-qPCR. Then, the functions of overexpressed CHRF in NEF-disposed cells were determined. At last, impacts of NEF on PI3K/AKT/mTOR and ERK1/2 pathways were evaluated. Results showed that NEF restrained cell proliferation, triggered apoptosis and repressed migration and invasion in JEG-3 and HTR-8 cells. CHRF was ascended in choriocarcinoma tissues and NEF repressed CHRF expression in choriocarcinoma cell lines. Additionally, overexpressed CHRF abolished the above functions of NEF in choriocarcinoma cells proliferation, apoptosis, migration and invasion. Further, NEF impeded PI3K/AKT/mTOR and ERK1/2 pathways via repressing CHRF. The explorations testified that NEF exhibited the anti-tumour action in JEG-3 and HTR-8 cells via hindering PI3K/AKT/mTOR and ERK1/2 pathways by mediating CHRF.
引用
收藏
页码:4089 / 4096
页数:8
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