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时间:2020-06-03
《STAT信号通路基因的影响.pdf》由会员上传分享,免费在线阅读,更多相关内容在应用文档-天天文库。
1、中国骨质疏松杂志2014年7月第20卷第7期ChinJOsteoporos,July2014,Vol20,No.7PublishedonlineWWW.wanfangdate.CO/1].e//doi:10.3969/j,issn.1006-7108,2014.07.00574l·论著·六味地黄丸对绝经后骨质疏松症肾阴虚证JAK/STAT信号通路基因的影响谢丽华陈娟李生强许惠娟范超领赖玉链葛继荣福建省中医药研究院骨质疏松证候基因组学研究室,福州350003中图分类号:R681文献标识码:A文章编号:1006—
2、7108(2014)07-0741—06摘要:目的通过观察六味地黄丸对绝经后骨质疏松症肾阴虚证JAK/STAT信号通路基因的影响,探讨六味地黄丸治疗绝经后骨质疏松症肾阴虚证的分子机制。方法随机选择绝经后骨质疏松症。肾阴虚证组6例,健康绝经后妇女对照组3例。六味地黄丸治疗肾阴虚证组3个月后,用JAK/STAT信号通路芯片检测其基因表达的变化。结果治疗前肾阴虚证组与正常对照组相比,差异表达基因:PRLR、JUN、JUNB、INSR,表达均下调;肾阴虚证组治疗后与治疗前相比,差异表达基因有25条,上调11条,下调1
3、4条,其中JUN、JUNB疗后明显上调。差异表达基因生物学功能分析,免疫相关基因:PRL、PRLR、OSM、1SG15、IL4R;细胞生长增殖与细胞周期相关基因:F2、SOCS3;与STAT蛋白相互作用的转录因子和共同活化基因:JUN、JUNB、SMAD3、SMAD5、SMAD4、SP1、YY1;JAK/STAT信号通路的负反馈调节基因:PIAS1、SOCS4;衔接蛋白基因:SRC、STAM。结论六味地黄丸治疗绝经后骨质疏松症肾阴虚证的机制可能与其调控JAK/STAT信号通路的相关基因有关,这些基因的功能与免
4、疫调节、细胞生长增殖及成骨生长关联。关键词:六味地黄丸;绝经后骨质疏松症;肾阴虚证;JAK/STAT信号通路芯片EffectofLiuweidihuangpillonJAK/STATsignalingpathwaygeneexpressioninpostmenopausalosteoporosiswiththekidneyyindeficiencyXIELihua,CHENJuan,LIShengqiang,XUHuijuan,FANChaoling,LAIYulian,GEJirongKeyResearch
5、LaboratoryofOsteoporosisSyndromeGenomics,FujianAcademyofTraditionalChineseMedicine,Fuzhou350003,ChinaCorrespondingauthor:GEJirong,Email:gjrogcy@sohu.comAbstract:ObjectiveToinvestigatetheefectofLiuweidihuangpillonJAK/STATsignalingpathwaygeneexpressioninpostm
6、enopausalosteoporosiswiththekidneyyindeficiency,andtoexplorethemolecularmechanismofLiuweidihuangpillinthetreatmentofpostmenopausalosteoporosiswiththekidneyyindeficiency.MethodsAccordingtotheTCMsyndrome,6womenwiththekidneyyindeficiencyandpostmenopausalosteop
7、orosiswererandomlyselected.Another3healthypostmenopausalwomenwereselectedascontrolgroup.PatientswiththekidneyyindeficiencyweretreatedwithLiuweidihuangpillfor3months.ThegeneexpressioninJAK/STATsignalingpathwaywasdetectedusingspecialchip.ResultsComparedwithth
8、oseincontrolgroup,theexpressionof4differentialgeneswasdown·regulatedinthekidneyyindeficiencygroupbeforethetreatment,includingPRLR,JUN,JUNB,andINSR.Afterthe~eatment,25differentiallyexpressedgeneswereide
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