中华皮肤科杂志
中華皮膚科雜誌
중화피부과잡지
Chinese Journal of Dermatology
2010年
2期
82-84
,共3页
王焱%孙建方%方方%韩峻松%张国成
王焱%孫建方%方方%韓峻鬆%張國成
왕염%손건방%방방%한준송%장국성
微RNAs%黑色素瘤%微芯片
微RNAs%黑色素瘤%微芯片
미RNAs%흑색소류%미심편
MicroRNAs%Melanoma%Microchip
目的 筛选人皮肤黑素瘤组织中表达的已知has-microRNA.方法 采用SBC microRNA芯片技术,将6例人皮肤黑素瘤组织总RNA分别与9例健康人色素痣总RNA混合物对比,筛选已知的468条has-microRNA表达情况.用qPCR分别检测这6例人皮肤黑素瘤组织中各候选has-microRNA的表达.将芯片和qPCR两种方法 检测结果一致的候选has-microRNA确定为有意义的共同差异表达has-microRNA.结果 2倍以上差异表达miRNA占所检测miRNA的12.18%~86.33%,5倍以上差异表达miRNA占1.28%~19.02%,10倍以上差异表达miRNA占0.43%~5.34%.此6例人皮肤黑素瘤中miRNA-21明显上调表达,miRNA-320和miRNA-494明显下调表达.结论 人皮肤黑素瘤组织中miRNA-21明显上调表达,miRNA-320和miRNA-494明显下调表达.
目的 篩選人皮膚黑素瘤組織中錶達的已知has-microRNA.方法 採用SBC microRNA芯片技術,將6例人皮膚黑素瘤組織總RNA分彆與9例健康人色素痣總RNA混閤物對比,篩選已知的468條has-microRNA錶達情況.用qPCR分彆檢測這6例人皮膚黑素瘤組織中各候選has-microRNA的錶達.將芯片和qPCR兩種方法 檢測結果一緻的候選has-microRNA確定為有意義的共同差異錶達has-microRNA.結果 2倍以上差異錶達miRNA佔所檢測miRNA的12.18%~86.33%,5倍以上差異錶達miRNA佔1.28%~19.02%,10倍以上差異錶達miRNA佔0.43%~5.34%.此6例人皮膚黑素瘤中miRNA-21明顯上調錶達,miRNA-320和miRNA-494明顯下調錶達.結論 人皮膚黑素瘤組織中miRNA-21明顯上調錶達,miRNA-320和miRNA-494明顯下調錶達.
목적 사선인피부흑소류조직중표체적이지has-microRNA.방법 채용SBC microRNA심편기술,장6례인피부흑소류조직총RNA분별여9례건강인색소지총RNA혼합물대비,사선이지적468조has-microRNA표체정황.용qPCR분별검측저6례인피부흑소류조직중각후선has-microRNA적표체.장심편화qPCR량충방법 검측결과일치적후선has-microRNA학정위유의의적공동차이표체has-microRNA.결과 2배이상차이표체miRNA점소검측miRNA적12.18%~86.33%,5배이상차이표체miRNA점1.28%~19.02%,10배이상차이표체miRNA점0.43%~5.34%.차6례인피부흑소류중miRNA-21명현상조표체,miRNA-320화miRNA-494명현하조표체.결론 인피부흑소류조직중miRNA-21명현상조표체,miRNA-320화miRNA-494명현하조표체.
Objective To select microRNAs (miRNA) associated with human cutaneous malignant melanoma (MM). Methods Total RNA was extracted from 6 tissue samples of MM and 9 human control samples of pigmented nevi, and small RNAs of less than 200 bp were enriched, miRNA microarray was used to select differentially expressed miRNAs between tissue samples of MM and pigmented nevi from 468 candi-dates. The expression of differentially expressed miRNAs was confirmed by fluorescence based real-time quan-titative PCR (qPCR) in all of these samples. Those miRNAs that were identified as differentially expressed with both miRNA microarray and qPCR were considered as significant miRNAs. Results Between the tissue samples of MM and pigmented nevi, 12.18% to 86.33% of miRNAs differentially expressed by more than 2 folds, 1.28% to 19.02% by more than 5 folds, and 0.43% to 5.34% by more than 10 folds. The expression of miRNA-21 was obviously up-regulated, while that of miRNA-320 and miRNA-494 was down-regulated in the MM samples. Conclusion There is an increase in the expression of homo sapiens miRNA-21 but a decrease in that of miRNA-320 and miRNA-494 in MM tissues.