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澳洲茄胺对人骨肉瘤移植瘤的抑制作用及其机制
引用本文:杨利,李小健,李朝军. 澳洲茄胺对人骨肉瘤移植瘤的抑制作用及其机制[J]. 安徽医药, 2021, 25(4): 664-668. DOI: 10.3969/j.issn.1009-6469.2021.04.007
作者姓名:杨利  李小健  李朝军
作者单位:唐山市丰润区第二人民医院骨科,河北 唐山064000
摘    要:目的 探讨澳洲茄胺对人骨肉瘤移植瘤的抑制作用及其机制.方法 该研究于2018年1月至2019年3月完成.MG63细胞株购于中科院上海细胞库.将0.2 mL人骨肉瘤MG63细胞悬液(共2×106个细胞)注射于裸鼠右侧腋窝皮下,建立人骨肉瘤移植瘤模型,实验分为4组,即对照组和澳洲茄胺组(10 mg/kg、20 mg/kg、...

关 键 词:澳洲茄胺  龙葵  人骨肉瘤细胞  细胞凋亡  血管内皮生长因子  凝血酶敏感蛋白1

Inhibitory effect of solasodine on human osteosarcoma xenografts and its mechanism
YANG Li,LI Xiaojian,LI Chaojun. Inhibitory effect of solasodine on human osteosarcoma xenografts and its mechanism[J]. Anhui Medical and Pharmaceutical Journal, 2021, 25(4): 664-668. DOI: 10.3969/j.issn.1009-6469.2021.04.007
Authors:YANG Li  LI Xiaojian  LI Chaojun
Affiliation:Department of Orthopaedics, Second People''s Hospital of Tangshan Fengrun District, Tangshan, Hebei 064000, China
Abstract:Objective To explore the inhibitory effect of solasodine on human osteosarcoma xenografts and its mechanism.Meth? ods The study was completed from January 2018 to March 2019. The MG63 cell line was purchased from Shanghai Cell Bank of Chinese Academy of Sciences. The human osteosarcoma MG63 cell suspension (0.2 mL, 2×106 cells) was injected subcutaneously into theright armpit of nude mice to establish human osteosarcoma xenograft model. The experiment was assigned into four groups: controlgroup and solasodine group (10 mg/kg, 20 mg/kg, 40 mg/kg). The mice were injected intraperitoneally once every other day for 4 weeks.The weight and volume of xenografts were measured. Apoptosis was detected by terminal-deoxynucleotidyl transferase mediated nick end labeling (TUNEL) staining. The expression of apoptosis-related proteins, angiogenesis-related factors and phosphoinositide-3-kinase/serine-threonine kinase (PI3K/AKT) signaling pathway were detected by Western blotting.Results Compared with control group, the weight (0.45±0.12) g and volume (510.62±95.78) mm3 at 21 d and (579.56±92.04) mm3 at 28 d of the xenografts in the solasodine group decreased, and the inhibitory effect of 40 mg/kg group was the most obvious (P<0.05). The fluorescence intensity of terminal-deoxynucleotidyl transferase mediated nick end labeling-fluorescein-isothiocyanate (TUNEL-FITC) in the solasodine group was higher thanthat in the control group, especially in the 40 mg/kg group. The protein expression of B cell lymphoma/leukemia-2 associated X protein (Bax) (3.55±0.39), cleaved cystein-asparate protease-3 (Cleaved caspase-3) (3.94±0.33), cleaved cystein-asparate protease-9 (Cleaved caspase-9) (3.59±0.31), thrombospondin 1 (TSP-1) (3.70±0.41) were up-regulated, while the protein expression of B cell lymphoma/leukemia-2 (Bcl-2) (0.31±0.15), vascular endothelial growth factor (VEGF) (0.25±0.12), phosphorylated phosphoinositide-3-kinase (p-PI3K) (0.39±0.12) and phosphorylated serine-threonine kinase (p-AKT) (0.33±0.11) were down-regulated, and the effect of 40 mg/kg group was the most obvious (P<0.05).Conclusion Solasodine can inhibit the growth of human osteosarcoma cells, induce apoptosis, down-regulate the expression of VEGF and up-regulate the expression of TSP-1, which may be related to the inhibition of PI3K/AKT signaling pathway.
Keywords:Solasodine   Solanum nigrum   Human osteosarcoma cells   Cell apoptosis   Vascular endothelial growth factor (VEGF)   Thrombospondin 1 (TSP-1)
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