TRAIL与caspase-8在人骨肉瘤中表达的相关性及其与细胞增殖和凋亡的关系

X. Ning, X. Shang, Y. Zhuang, M. Liu, Hua Yang, Hao Zhang, M. Huang
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引用次数: 1

摘要

骨肉瘤是一种常见的恶性骨肿瘤,主要影响儿童和青少年。肿瘤坏死因子相关凋亡诱导配体(TRAIL)是肿瘤坏死因子超家族的一员。Caspase-8在caspase中出现在凋亡信号通路的上游。我们研究了骨肉瘤患者的TRAIL和caspase-8水平,以确定它们与细胞增殖和凋亡的关系。选择在我院接受手术的骨肉瘤和骨软骨瘤患者。免疫组化法检测组织中TRAIL和caspase-8的表达水平,免疫印迹法检测细胞中蛋白水平。采用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四唑(MTT)法测定人骨肉瘤细胞活力。流式细胞术观察骨肉瘤和骨软骨瘤细胞周期和凋亡情况。对细胞凋亡过程中TRAIL与caspase-8水平进行相关性分析。TRAIL和caspase-8在骨肉瘤组织中的阳性表达率显著低于对照组(P < 0.05)。实验细胞中TRAIL(0.114±0.002)和caspase-8(0.352±0.124)水平明显低于对照组(P < 0.05)。实验组骨肉瘤细胞在24h、48h和72h的增殖率较高,凋亡率较低(P < 0.05)。G1期实验细胞数增多,S期实验细胞数减少(P < 0.05)。TRAIL、caspase-8蛋白与骨肉瘤细胞凋亡呈正相关(P < 0.05)。人骨肉瘤表现为TRAIL和caspase-8水平降低,细胞增殖增强,细胞凋亡减少。TRAIL和caspase-8表达水平与骨肉瘤细胞凋亡呈正相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Correlation between TRAIL and caspase-8 expression and their relationship with cell proliferation and apoptosis in human osteosarcoma.
Osteosarcoma is a common malignant bone tumor that mainly affects children and adolescents. Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) is a member of the tumor necrosis factor superfamily. Caspase-8 appears in the upstream of apoptosis signaling pathway among caspases. We investigated TRAIL and caspase-8 levels in osteosarcoma patients to determine their correlation with cell proliferation and apoptosis. Osteosarcoma and osteochondroma patients receiving surgery in our hospital were selected. TRAIL and caspase-8 expression levels in tissue were determined by immunohistochemistry, and protein levels in cells were evaluated by western blotting. Human osteosarcoma cell viability was determined by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. The osteosarcoma and osteochondroma cell cycles and apoptosis were investigated by flow cytometry. Correlation analysis was applied to TRAIL and caspase-8 levels during cell apoptosis. Positive TRAIL and caspase-8 expression rates in osteosarcoma tissue were significantly lower than in the controls (P < 0.05). TRAIL (0.114 ± 0.002) and caspase-8 (0.352 ± 0.124) levels in experimental cells were obviously lower than in the controls (P < 0.05). Osteosarcoma cells in the experimental group demonstrated higher proliferation and lower apoptosis at 24, 48, and 72 h (P < 0.05). The experimental cell number increased in the G1 stage and decreased in the S stage (P < 0.05). TRAIL and caspase-8 proteins showed positive correlation with apoptosis in osteosarcoma (P < 0.05). Human osteosarcoma presented reduced TRAIL and caspase-8 levels with enhanced cell proliferation and reduced apoptosis. TRAIL and caspase-8 expression levels were positively correlated with apoptosis in osteosarcoma.
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