He Cheng-Wei, Liu Fang, Zhang Yue-Fei, Liang Tong, Zhou Ke-Yuan
Institute of Biochemistry and Molecular Biology, Guangdong Medical College, Zhanjiang, Guangdong 524023, P. R. China.
Ai Zheng. 2005 Jun;24(6):646-52.
BACKGROUND & OBJECTIVE: Recent studies showed overexpression of bcl-x(L) in human nasopharyngeal carcinoma (NPC) cell line CNE-2Z; it may play a pivotal role in tumorigenesis, metastasis, and drug resistance of NPC. This study was to explore inducing effect of bcl-x(L) short hairpin RNA (shRNA) on apoptosis of CNE-2Z cells.
After transfection of recombinant plasmid pmU6-RNAi expressing bcl-x(L) shRNA, apoptotic CNE-2Z cells were detected by fluorescent staining and flow cytometry (FCM). mRNA levels of bcl-x(L), bcl-2, survivin, and caspase-3 was detected by reverse transcription-polymerase chain reaction (RT-PCR); while protein levels of Bcl-x(L), Caspase-3, and P53 were detected by Western blot.
When treated with pmU6-RNAi for 24 h, an obvious apoptotic peak of CNE-2Z cells appeared; cell shrinkage, chromatin condensation, and nuclear fragmentation were observed in most cells under fluorescent microscope. RT-PCR analysis showed that pmU6-RNAi down-regulated mRNA levels of bcl-x(L), bcl-2, and caspase-3, but had little or no effect on mRNA level of survivin; Western blot analysis showed an obvious reduction in protein levels of Bcl-x(L) and Caspase-3, and a great increase in protein level of P53.
bcl-x(L) shRNA can induce apoptosis of CNE-2Z cells, which may be closely related to down-regulation of bcl-2, caspase-3 and p53. bcl-x(L) shRNA may be helpful for developing gene therapy for NPC.
近期研究显示,人鼻咽癌(NPC)细胞系CNE-2Z中bcl-x(L)呈过表达;其可能在NPC的肿瘤发生、转移及耐药中起关键作用。本研究旨在探讨bcl-x(L)短发夹RNA(shRNA)对CNE-2Z细胞凋亡的诱导作用。
转染表达bcl-x(L) shRNA的重组质粒pmU6-RNAi后,采用荧光染色和流式细胞术(FCM)检测CNE-2Z凋亡细胞。采用逆转录-聚合酶链反应(RT-PCR)检测bcl-x(L)、bcl-2、survivin及caspase-3的mRNA水平;采用蛋白质印迹法检测Bcl-x(L)、Caspase-3及P53的蛋白质水平。
用pmU6-RNAi处理24小时后,CNE-2Z细胞出现明显的凋亡峰;荧光显微镜下可见多数细胞出现细胞皱缩、染色质凝聚及核碎裂。RT-PCR分析显示,pmU6-RNAi下调bcl-x(L)、bcl-2及caspase-3的mRNA水平,但对survivin的mRNA水平影响很小或无影响;蛋白质印迹分析显示,Bcl-x(L)和Caspase-3的蛋白质水平明显降低,P53的蛋白质水平显著升高。
bcl-x(L) shRNA可诱导CNE-2Z细胞凋亡,这可能与bcl-2、caspase-3及p53的下调密切相关。bcl-x(L) shRNA可能有助于开展NPC的基因治疗。