首页|葡萄球菌核酸酶样结构蛋白1/SLC7A11抑制铁死亡对骨肉瘤发生发展的影响

葡萄球菌核酸酶样结构蛋白1/SLC7A11抑制铁死亡对骨肉瘤发生发展的影响

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目的 探讨葡萄球菌核酸酶样结构蛋白1(SND1)对骨肉瘤细胞生物学功能的影响,及其通过SLC7A11 调控骨肉瘤细胞铁死亡的作用机制.方法 检测人成骨细胞hFOB1.19 以及骨肉瘤细胞系Saos-2、U2OS、HOS和 143B中SND1 的表达水平.采用小干扰RNA敲减骨肉瘤细胞HOS和143B中SND1 的表达(si-SND1),采用CCK8 法、细胞克隆形成实验、细胞迁移和侵袭实验探究 SND1 的表达对骨肉瘤细胞生物学功能的影响;调控骨肉瘤细胞中 SND1 以及SLC7A11 基因的表达,探究SND1 通过SLC7A1 基因对骨肉瘤铁死亡介导的肿瘤细胞凋亡的影响.结果 骨肉瘤细胞Saos-2、U2OS、HOS和143B中SND1 mRNA和蛋白的表达水平显著高于人成骨细胞hFOB1.19(P均<0.01).与对照组比较,si-SND1 转染显著降低HOS和143B细胞中SND1 的表达水平(P均<0.01),且细胞活性显著降低,克隆形成数量显著减少,细胞迁移和侵袭能力显著降低(P均<0.001).铁死亡诱导剂Erastin促进骨肉瘤HOS和143B细胞凋亡,而抑制剂Fer-rostatin-1 刺激上调细胞活性(P均<0.001).敲减SND-1 后使用Erastin可进一步降低骨肉瘤HOS和143B细胞活性,而使用Ferrostatin-1 刺激后可显著恢复细胞活性(P均<0.001);Erastin处理后,si-SND1 组细胞中铁离子和丙二醛表达增高,谷胱甘肽表达降低(P均<0.001).体内实验结果显示,敲减SND1 可以明显抑制143B裸鼠移植瘤的瘤体质量(P<0.001).敲减SND1 后骨肉瘤HOS和143B细胞中SLC7A11 的表达水平显著减少(P均<0.001),且铁死亡水平升高(P<0.001,P=0.020).结论 骨肉瘤细胞中SND1表达显著增高,其可能通过上调SLC7A11的表达抑制铁死亡,进而促进骨肉瘤细胞活性.
Effect of Staphylococcal Nuclease and Tudor Domain Containing 1/SLC7A11 on the Occurrence and Development of Osteosarcoma by Inhibiting Ferroptosis
Objective To investigate the effect of staphylococcal nuclease and tudor domain containing 1(SND1)on the biological function of osteosarcoma cells and decipher the mechanism of SND1 in regulating fer-roptosis in osteosarcoma cells via SLC7A11.Methods Human osteoblasts hFOB1.19 and osteosarcoma cell lines Saos-2,U2OS,HOS,and 143B were cultured,in which the expression level of SND1 was determined.Small in-terfering RNA was employed to knock down the expression of SND1(si-SND1)in the osteosarcoma cell line HOS and 143B.The CCK8 assay kit,colony formation assay,and Transwell assay were employed to examine the effect of SND1 expression on the biological function of osteosarcoma cells.Furthermore,we altered the expression of SND1 and SLC7A11 in osteosarcoma cells to investigate the effect of SND1 on osteosarcoma ferroptosis via SLC7A11.Results The mRNA and protein levels of SND1 in Saos-2,U2OS,HOS,and 143B cells were higher than those in hFOB1.19 cells(all P<0.01).Compared with the control group,transfection with si-SND1 down-regulated the expression level of SND1 in HOS and 143B cells(all P<0.01),decreased the viability of HOS and 143B cells,reduced the number of colony formation,and inhibited cell invasion and migration(all P<0.001).The ferroptosis inducer Erastin promoted the apoptosis of HOS and 143B cells,while the ferroptosis inhibitor Fer-rostatin-1 improved the viability of HOS and 143B cells(all P<0.001).After SND-1 knockdown,Erastin reduced the viability of HOS and 143B cells,while Ferrostatin-1 restored the cell viability(all P<0.001).After treatment with Erastin in the si-SND1 group,the levels of iron and malondialdehyde were elevated,and the level of glutathione was lowered(all P<0.001).The results of in vivo experiments showed that SND1 knockdown inhibited the mass of the transplanted tumor in 143B tumor-bearing nude mice(P<0.001).Knocking down the expression of SND1 resul-ted in down-regulated SLC7A11 expression(all P<0.001)and increased ferroptosis in HOS and 143B cells(P<0.001,P=0.020).Conclusions SND1 presents up-regulated expression in osteosarcoma cells.It may inhibit ferrop-tosis by up-regulating the expression of SLC7A11,thereby improving the viability of osteosarcoma cells.

osteosarcomastaphylococcal nuclease and tudor domain containing 1ferroptosis

王胜涛、徐淑娟、贵鹏、李欣咛、隋玉涵、李朝旭

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广西壮族自治区南溪山医院关节外科与运动医学科, 广西桂林 541002

桂林医学院附属医院血液内科, 广西桂林 541001

广西壮族自治区南溪山医院创伤骨科与手外科, 广西桂林 541002

广西中医药大学研究生院, 南宁 530200

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骨肉瘤 葡萄球菌核酸酶样结构蛋白1 铁死亡

广西医疗卫生重点学科建设项目广西医疗卫生重点培育学科建设项目

桂卫教科发[2022]4号桂卫教科发[2022]4号

2024

中国医学科学院学报
中国医学科学院,北京协和医学院

中国医学科学院学报

CSTPCD北大核心
影响因子:1.496
ISSN:1000-503X
年,卷(期):2024.46(1)
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