广州医科大学学报
廣州醫科大學學報
엄주의과대학학보
Academic Journal of Guangzhou Medical College
2014年
4期
13-18
,共6页
肖耀军%陈壮飞%郑少斌%王海坤%黄谷%李彬
肖耀軍%陳壯飛%鄭少斌%王海坤%黃穀%李彬
초요군%진장비%정소빈%왕해곤%황곡%리빈
miRNA%肾透明细胞癌%miRNA芯片%实时定量RT-PCR
miRNA%腎透明細胞癌%miRNA芯片%實時定量RT-PCR
miRNA%신투명세포암%miRNA심편%실시정량RT-PCR
miRNA%renal clear cell carcinoma%miRNA array%real-time quantitative PCR
目的:筛选肾透明细胞癌组织差异表达的miRNAs,并分析其与可能的靶基因作用调控关系。方法:收集8例新鲜的肾透明细胞癌及其癌旁正常肾组织,抽提总RNA,并行Hy3荧光标记,将标记的小RNA与包含1891条探针的miRNA芯片进行杂交,再扫描及数据分析处理。 miRNA芯片结果的可靠性采用RT-PCR方法验证。结果:肾透明细胞癌组织与癌旁正常肾组织比较,存在较多明显差异表达的miRNAs,其中上调miRNAs 106个、下调miRNAs 184个,其中111个miRNAs为16.0版miRNA芯片新增的;显著上调的miRNAs 3个、下调的miRNAs 38个。结论:肾透明细胞癌组织的miRNA表达谱有较强特异性,其与可能的靶基因调控关系复杂,其中miR-155、miR-141、miR-200c及let-7家族等与肾透明细胞癌的发病密切相关。
目的:篩選腎透明細胞癌組織差異錶達的miRNAs,併分析其與可能的靶基因作用調控關繫。方法:收集8例新鮮的腎透明細胞癌及其癌徬正常腎組織,抽提總RNA,併行Hy3熒光標記,將標記的小RNA與包含1891條探針的miRNA芯片進行雜交,再掃描及數據分析處理。 miRNA芯片結果的可靠性採用RT-PCR方法驗證。結果:腎透明細胞癌組織與癌徬正常腎組織比較,存在較多明顯差異錶達的miRNAs,其中上調miRNAs 106箇、下調miRNAs 184箇,其中111箇miRNAs為16.0版miRNA芯片新增的;顯著上調的miRNAs 3箇、下調的miRNAs 38箇。結論:腎透明細胞癌組織的miRNA錶達譜有較彊特異性,其與可能的靶基因調控關繫複雜,其中miR-155、miR-141、miR-200c及let-7傢族等與腎透明細胞癌的髮病密切相關。
목적:사선신투명세포암조직차이표체적miRNAs,병분석기여가능적파기인작용조공관계。방법:수집8례신선적신투명세포암급기암방정상신조직,추제총RNA,병행Hy3형광표기,장표기적소RNA여포함1891조탐침적miRNA심편진행잡교,재소묘급수거분석처리。 miRNA심편결과적가고성채용RT-PCR방법험증。결과:신투명세포암조직여암방정상신조직비교,존재교다명현차이표체적miRNAs,기중상조miRNAs 106개、하조miRNAs 184개,기중111개miRNAs위16.0판miRNA심편신증적;현저상조적miRNAs 3개、하조적miRNAs 38개。결론:신투명세포암조직적miRNA표체보유교강특이성,기여가능적파기인조공관계복잡,기중miR-155、miR-141、miR-200c급let-7가족등여신투명세포암적발병밀절상관。
Objective:To investigate the differentially expressed miRNAs and analyze their regulatory relations with possible target genes.Methods: Total RNA was extracted from 8 fresh samples of renal clear cell carcinoma and adjacent nontumorous tissues. Small miRNAs were isolated from total RNA, labeled with Hy3 and hybridized with the miRNA array, which included 1891 probes, for screening and data processing and analyzing. Real-time quantitative PCR ( RT-PCR) was applied to validate the reliability of miRNA array results. Results:Compared to normal adjacent tissues, miRNAs were differentially expressed in cc-RCC, including 106 up-regulated and 184 down-regulated miRNAs, with 111 added miRNAs of 16. 0 version miRNA array. 3 miRNAs were significantly up-regulated and 38 miRNAs were significantly down-regulated. Conclusion: The miRNA expression profile of human cc-RCC has strong specificity, which has complex relationship with possible target genes. Such as miR-155, miR-141, miR-200c and let-7 family, etc, may be closely related to the pathogenesis and development of cc-RCC.