Pratika Yuhyi Hernanda
{"title":"ANALISIS EKSPRESI PROTEIN TLR-9, CD90 DAN VEGF PADA MESENCHYMAL STEM CELL DI JARINGAN TUMOR OSTEOSARKOMA","authors":"Pratika Yuhyi Hernanda","doi":"10.30742/JIKW.V8I2.625","DOIUrl":null,"url":null,"abstract":"For further investigation on the effect of Mesenchymal Stem Cell (MSC) on tumor / cancer growth, it is necessary to start with tumor MSC profile from tumor / cancer tissue. In this study, we use MSC from osteosarcoma tissue as a representative. The MSC profile analysis method used were the comparing the phenotype and characteristics of MSC fromosteosarcoma tissue with MSC from normal adiposa tissue. The characteristics of MSC were represented by protein expression of several candidate genes namely TLR-9, CD-90 and VEGF. From the results of immunofluorescence staining on adiposa MSC compared withosteosarcoma MSC, it has obviously seen that although the phenotypes were similar, there was no significant difference in CD-90 expression in osteosarcoma MSC and adiposa MSC. Although VEGF expression appears to be slightly prominent in osteosarcoma MSCs, the difference between the two was also not significant. Whereas TLR9 expression is very prominent in osteosarcoma MSC and significantly different from adiposa MSC. Thus TLR9 may be of concern in subsequent studies to investigate the mechanism of MSC triggers tumor growth.","PeriodicalId":33090,"journal":{"name":"Jurnal Ilmiah Kedokteran Wijaya Kusuma","volume":"12 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Jurnal Ilmiah Kedokteran Wijaya Kusuma","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.30742/JIKW.V8I2.625","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

为了进一步研究间充质干细胞(Mesenchymal Stem Cell, MSC)对肿瘤/癌症生长的影响,有必要从肿瘤/癌症组织的MSC谱开始。在本研究中,我们使用来自骨肉瘤组织的MSC作为代表。所采用的间充质谱分析方法是比较来自骨肉瘤组织的间充质与来自正常脂肪组织的间充质的表型和特征。MSC的特征主要体现在几个候选基因TLR-9、CD-90和VEGF的蛋白表达上。从脂肪间充质干细胞和脂肪间充质干细胞的免疫荧光染色结果可以明显看出,虽然表型相似,但CD-90在骨肉瘤间充质干细胞和脂肪间充质干细胞中的表达没有显著差异。虽然VEGF在骨肉瘤MSCs中的表达略显突出,但两者之间的差异也不显著。而TLR9在骨肉瘤间充质干细胞中的表达非常突出,与脂肪间充质干细胞有显著差异。因此,TLR9可能是后续研究MSC触发肿瘤生长机制的重点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ANALISIS EKSPRESI PROTEIN TLR-9, CD90 DAN VEGF PADA MESENCHYMAL STEM CELL DI JARINGAN TUMOR OSTEOSARKOMA
For further investigation on the effect of Mesenchymal Stem Cell (MSC) on tumor / cancer growth, it is necessary to start with tumor MSC profile from tumor / cancer tissue. In this study, we use MSC from osteosarcoma tissue as a representative. The MSC profile analysis method used were the comparing the phenotype and characteristics of MSC fromosteosarcoma tissue with MSC from normal adiposa tissue. The characteristics of MSC were represented by protein expression of several candidate genes namely TLR-9, CD-90 and VEGF. From the results of immunofluorescence staining on adiposa MSC compared withosteosarcoma MSC, it has obviously seen that although the phenotypes were similar, there was no significant difference in CD-90 expression in osteosarcoma MSC and adiposa MSC. Although VEGF expression appears to be slightly prominent in osteosarcoma MSCs, the difference between the two was also not significant. Whereas TLR9 expression is very prominent in osteosarcoma MSC and significantly different from adiposa MSC. Thus TLR9 may be of concern in subsequent studies to investigate the mechanism of MSC triggers tumor growth.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
13
审稿时长
6 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信