目的：通过观察慢性阻塞性肺疾病（COPD）稳定期患者、COPD合并肺动脉高压（PH）患者及健康者之间SOX5基因单核苷酸多态性（SNPs）的分布差异,初步探索SOX5基因多态性与COPD相关PH易感性的关联。方法：连续选择2013年4月~2015年4月就诊...目的：通过观察慢性阻塞性肺疾病（COPD）稳定期患者、COPD合并肺动脉高压（PH）患者及健康者之间SOX5基因单核苷酸多态性（SNPs）的分布差异,初步探索SOX5基因多态性与COPD相关PH易感性的关联。方法：连续选择2013年4月~2015年4月就诊于宁夏人民医院总院及宁南分院呼吸内科的COPD稳定期患者250例,根据COPD诊治指南（2013年版）诊断标准入组,并且就诊当天全部进行超声心动图检查,根据肺动脉收缩压（PASP）结果分为COPD合并PH组（PASP≥50 mm Hg）103例和COPD非PH组（PASP〈50 mm Hg）147例。健康对照组选择同期在宁夏人民医院体检的健康者127例。使用Sequenom Mass ARRAY SNP检测系统检测所有受试者SOX5基因rs10842262和rs11046966位点的基因型,统计基因型频率并对比各组间差异。结果：健康对照组与COPD组之间（包括COPD合并PH及未合并PH组的全部患者）以及COPD合并PH组与COPD非PH组之间在年龄、性别和吸烟指数上的差别均无统计学显著性。健康对照组与COPD组之间SOX5基因rs10842262位点及rs11046966位点基因型频率分布的差异均存在统计学显著性（P〈0.05）。COPD合并PH组与COPD非PH组之间SOX5基因rs10842262位点及rs11046966位点各基因型频率分布的差异无统计学显著性。结论：SOX5基因rs10842262和rs11046966位点的基因多态性与COPD的易感性相关,但与COPD相关PH的易感性还不能认为有关联。展开更多
目的观察Y染色体上的性别决定区相关高迁移率族盒蛋白-5(sex determining region Ybox protein 5,SOX5)对骨肉瘤细胞MG63迁移和侵袭能力的影响,探讨其在骨肉瘤发病和转移中的作用。方法本研究为前瞻性研究,通过脂质体介导的基因转染技术...目的观察Y染色体上的性别决定区相关高迁移率族盒蛋白-5(sex determining region Ybox protein 5,SOX5)对骨肉瘤细胞MG63迁移和侵袭能力的影响,探讨其在骨肉瘤发病和转移中的作用。方法本研究为前瞻性研究,通过脂质体介导的基因转染技术将SOX5的三个不同的siRNA(siSOX5-1、siSOX5-2和siSOX5-3)瞬时转染骨肉瘤细胞MG63,转染后48 h检测SOX5的mRNA和蛋白表达,从中挑选出干扰效果最明显的siRNA。进而采用博伊登室实验方法分别对干扰前后的骨肉瘤细胞MG63进行体外细胞迁移和侵袭测定,采用免疫印迹(Western blot)检测迁移和侵袭相关蛋白[基质金属蛋白酶(matrix metallproteinase,MMP)-2、MMP-9、Twist1和Snail1)]的表达水平。结果 3条针对人的siRNA(siSOX5-1、siSOX5-2、siSOX5-3)均能够降低SOX5 mRNA及蛋白水平表达,其中siSOX5-3干扰效果最明显。siSOX5-3干扰组的迁移细胞数为(52±5)较对照组的(107±9)显著减少(P<0.05),siSOX5-3干扰组的侵袭细胞数为(27±4)较对照组的(71±2)显著减少(P<0.05)。Western blot结果显示siSOX5-3干扰组的侵袭相关蛋白(MMP-2、MMP-9、Twist1和Snail1)的表达均较对照组显著降低(P<0.05)。结论SOX5 RNA干扰能显著降低骨肉瘤细胞的迁移和侵袭能力,SOX5能促进骨肉瘤细胞的迁移和侵袭。展开更多
Kaposi's sarcoma(KS) originates from vascular endothelial cells, with KS-associated herpesvirus(KSHV) as the etiological agent. SRY-box transcription factor 5(SOX5) plays different roles in various types of cancer...Kaposi's sarcoma(KS) originates from vascular endothelial cells, with KS-associated herpesvirus(KSHV) as the etiological agent. SRY-box transcription factor 5(SOX5) plays different roles in various types of cancer, although its role in KS remains poorly understood. In this study, we identified the role of SOX5 in KS tissues and KSHV-infected cells and elucidated the molecular mechanism. Thirty-two KS patients were enrolled in this study. Measurement of SOX5 m RNA and protein levels in human KS tissues and adjacent control tissues revealed lower levels in KS tissues, with KS patients having higher SOX5 level in the early stages of the disease compared to the later stages. And SOX5 m RNA and protein was also lower in KSHV-infected cells(iSLK-219 and iSLK-BAC) than normal cells(iSLK-Puro). Additionally, SOX5 overexpression inhibited cell proliferation and promoted apoptosis and decreased KSHV-infected cell migration and invasion. Moreover, we found that SOX5 overexpression suppressed the epithelial-to-mesenchymal transition of KSHV-infected cells. These results suggest SOX5 is a suppressor factor during KS development and a potential target for KS treatment.展开更多
文摘目的：通过观察慢性阻塞性肺疾病（COPD）稳定期患者、COPD合并肺动脉高压（PH）患者及健康者之间SOX5基因单核苷酸多态性（SNPs）的分布差异,初步探索SOX5基因多态性与COPD相关PH易感性的关联。方法：连续选择2013年4月~2015年4月就诊于宁夏人民医院总院及宁南分院呼吸内科的COPD稳定期患者250例,根据COPD诊治指南（2013年版）诊断标准入组,并且就诊当天全部进行超声心动图检查,根据肺动脉收缩压（PASP）结果分为COPD合并PH组（PASP≥50 mm Hg）103例和COPD非PH组（PASP〈50 mm Hg）147例。健康对照组选择同期在宁夏人民医院体检的健康者127例。使用Sequenom Mass ARRAY SNP检测系统检测所有受试者SOX5基因rs10842262和rs11046966位点的基因型,统计基因型频率并对比各组间差异。结果：健康对照组与COPD组之间（包括COPD合并PH及未合并PH组的全部患者）以及COPD合并PH组与COPD非PH组之间在年龄、性别和吸烟指数上的差别均无统计学显著性。健康对照组与COPD组之间SOX5基因rs10842262位点及rs11046966位点基因型频率分布的差异均存在统计学显著性（P〈0.05）。COPD合并PH组与COPD非PH组之间SOX5基因rs10842262位点及rs11046966位点各基因型频率分布的差异无统计学显著性。结论：SOX5基因rs10842262和rs11046966位点的基因多态性与COPD的易感性相关,但与COPD相关PH的易感性还不能认为有关联。
基金supported by the National Natural Science Foundation of China (U160311781560473)+1 种基金Xinjiang Production and Construction Corps Key Areas Innovation Team Project (2018CB002)Shihezi University International Cooperation Project (GJHZ201901)。
文摘Kaposi's sarcoma(KS) originates from vascular endothelial cells, with KS-associated herpesvirus(KSHV) as the etiological agent. SRY-box transcription factor 5(SOX5) plays different roles in various types of cancer, although its role in KS remains poorly understood. In this study, we identified the role of SOX5 in KS tissues and KSHV-infected cells and elucidated the molecular mechanism. Thirty-two KS patients were enrolled in this study. Measurement of SOX5 m RNA and protein levels in human KS tissues and adjacent control tissues revealed lower levels in KS tissues, with KS patients having higher SOX5 level in the early stages of the disease compared to the later stages. And SOX5 m RNA and protein was also lower in KSHV-infected cells(iSLK-219 and iSLK-BAC) than normal cells(iSLK-Puro). Additionally, SOX5 overexpression inhibited cell proliferation and promoted apoptosis and decreased KSHV-infected cell migration and invasion. Moreover, we found that SOX5 overexpression suppressed the epithelial-to-mesenchymal transition of KSHV-infected cells. These results suggest SOX5 is a suppressor factor during KS development and a potential target for KS treatment.
