Scutellaria barbata D. Don inhibits cervical cancer cell proliferation, migration, and invasion via miR-195-5p/LOXL2 axis

被引:4
|
作者
Xue, Shouyu [1 ]
Geng, Aimin [2 ]
Lian, Ting [1 ]
Liu, Yun [3 ]
机构
[1] Xian Med Univ, Clin Med Sch, Xinwang Rd 1, Xian 710021, Shaanxi, Peoples R China
[2] Changan Hosp, Dept Urol Surg, Xian 710016, Shaanxi, Peoples R China
[3] Shaanxi Prov Hosp Chinese Med, Dept Infect Dis, Xian 710003, Shaanxi, Peoples R China
关键词
Scutellaria barbata D; Don; cervical cancer; miR-195-5p; LOXL2; COLORECTAL-CANCER; MALIGNANT PROGRESSION; CHLOROFORM FRACTION; PROMOTES; BIOGENESIS; OXIDASE; GROWTH; LOXL2;
D O I
10.1093/toxres/tfac058
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Background Scutellaria barbata D. Don (SB) is a widely used herbal medicine in China, with various pharmacological effects such as anti-oxidation, anti-inflammation, and anti-cancer. This work is aimed to investigate the tumor-suppressive effect of SB in cervical cancer (CC) and to identify its underlying mechanisms. Methods and materials CC cell lines (HeLa and HT-3) were treated with different concentrations of SB chloroform extract (ECSB) (0, 0.2, 0.5 mg/ml). MiR-195-5p and LOXL2 mRNA expression in CC cell lines and tissue samples was detected by quantitative real-time polymerase chain reaction. Cell counting kit-8 experiment was utilized to examine cell viability; TUNEL assay and Transwell experiment was executed to examine cell apoptosis, migration, and invasion. Western blotting experiments were implemented to detect LOXL2 protein expression. Bioinformatics and dual-luciferase reporter gene experiment were executed to examine the binding relationship between miR-195-5p and LOXL2. Results ECSB repressed the viability, migration, and invasion of HeLa and HT-3 cells, and promoted cell apoptosis in a dose-dependent manner. MiR-195-5p was remarkably under-expressed in CC tissues and cells, and ECSB up-regulated miR-195-5p expression. MiR-195-5p inhibitors partially counteracted the suppressive effects of ECSB on the malignant phenotypes of HeLa and HT-3 cells. LOXL2 was a downstream target of miR-195-5p, and ECSB up-modulated LOXL2 expression by specifically repressing miR-195-5p. Conclusion SB restrains CC cell proliferation and metastasis and promotes cell apoptosis via miR-195-5p/LOXL2, which may be a potential therapeutic agent for CC treatment.
引用
收藏
页码:804 / 811
页数:8
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