南京中医药大学学报
南京中醫藥大學學報
남경중의약대학학보
JOURNAL OF NANJING UNIVERSITY OF TRADITIONAL CHINESE MEDICINE
2015年
3期
254-257
,共4页
过忆%周留勇%尤建良%薛博瑜
過憶%週留勇%尤建良%薛博瑜
과억%주류용%우건량%설박유
长链非编码 RNA%姜黄素%AK125910%肝癌细胞%凋亡
長鏈非編碼 RNA%薑黃素%AK125910%肝癌細胞%凋亡
장련비편마 RNA%강황소%AK125910%간암세포%조망
long non-coding RNA%curcumin%AK125910%hepatoma cell%apoptosis
目的:检测姜黄素诱导肝癌细胞凋亡中 lncRNA 表达谱的改变及关键 lncRNA 的筛选鉴定。方法使用不同浓度姜黄素刺激肝癌细胞株 HepG2不同时间后,提取总 RNA 进行 lncRNA 芯片杂交检测 lncRNA 表达谱的改变,筛选出差异表达 ln-cRNA;并利用 MTT 法和 TUNEL 染色观察 HepG2细胞的凋亡,Real-time PCR 验证差异表达的 lncRNA AK125910在其中的作用。结果与对照组细胞相比,姜黄素处理后的肝癌细胞中有5432条 lncRNA 表达出现改变,而其中变化倍数大于3的lncRNA 有8条,表达差异化最显著的是 lncRNA AK058003,上调7.62倍。在姜黄素诱导肝癌细胞凋亡中,lncRNA AK058003表达上调7.16倍,与芯片杂交结果基本一致。结论姜黄素诱导肝癌细胞凋亡过程中 lncRNA 表达谱出现显著变化,其中差异性表达最显著的 lncRNA AK058003可能参与了肝癌细胞的凋亡进程。
目的:檢測薑黃素誘導肝癌細胞凋亡中 lncRNA 錶達譜的改變及關鍵 lncRNA 的篩選鑒定。方法使用不同濃度薑黃素刺激肝癌細胞株 HepG2不同時間後,提取總 RNA 進行 lncRNA 芯片雜交檢測 lncRNA 錶達譜的改變,篩選齣差異錶達 ln-cRNA;併利用 MTT 法和 TUNEL 染色觀察 HepG2細胞的凋亡,Real-time PCR 驗證差異錶達的 lncRNA AK125910在其中的作用。結果與對照組細胞相比,薑黃素處理後的肝癌細胞中有5432條 lncRNA 錶達齣現改變,而其中變化倍數大于3的lncRNA 有8條,錶達差異化最顯著的是 lncRNA AK058003,上調7.62倍。在薑黃素誘導肝癌細胞凋亡中,lncRNA AK058003錶達上調7.16倍,與芯片雜交結果基本一緻。結論薑黃素誘導肝癌細胞凋亡過程中 lncRNA 錶達譜齣現顯著變化,其中差異性錶達最顯著的 lncRNA AK058003可能參與瞭肝癌細胞的凋亡進程。
목적:검측강황소유도간암세포조망중 lncRNA 표체보적개변급관건 lncRNA 적사선감정。방법사용불동농도강황소자격간암세포주 HepG2불동시간후,제취총 RNA 진행 lncRNA 심편잡교검측 lncRNA 표체보적개변,사선출차이표체 ln-cRNA;병이용 MTT 법화 TUNEL 염색관찰 HepG2세포적조망,Real-time PCR 험증차이표체적 lncRNA AK125910재기중적작용。결과여대조조세포상비,강황소처리후적간암세포중유5432조 lncRNA 표체출현개변,이기중변화배수대우3적lncRNA 유8조,표체차이화최현저적시 lncRNA AK058003,상조7.62배。재강황소유도간암세포조망중,lncRNA AK058003표체상조7.16배,여심편잡교결과기본일치。결론강황소유도간암세포조망과정중 lncRNA 표체보출현현저변화,기중차이성표체최현저적 lncRNA AK058003가능삼여료간암세포적조망진정。
ABSTRACT:OBJECTIVE To detect the apoptosis of liver cancer cell induced by curcumin and related lncRNA expression changes and key lncRNA spectrum screening.METHODS After using different concentrations of curcumin to stimulate HepG2 cells at different times,total RNA was extracted to determine the changes of ncRNA microarray expression profiling ;and cell apoptosis of HepG2 cells was measured by using MTT assay and TUNEL staining.Real-time PCR was performed to examine the differentially expressed lncRNA AK125910.RESULTS Compared with control cells,5432 lncRNA expression in HepG2 cells induced by curcumin were changed,in which eight lncRNAs showed fold change> 3,and the most significant ex-pression differences is lncRNA AK058003 by up-regulation of 7.62 times.Curcumin induced apoptosis in liver cancer and ln-cRNA AK058003 was upregulated by 7.16-fold,consistent with the results of microarray.CONCLUSION The lncRNA ex-pression profiling in curcumin-induced apoptosis of liver cancer was significant changed.Moreover,most significant differenti-ally expressed lncRNA AK058003 may be involved in apoptosis of liver cancer cells.