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Correlation between expression of DcR3 on tumor cells and sensitivity to FasL

机译:DcR3在肿瘤细胞上的表达与FasL敏感性的相关性

摘要

To investigate the correlation between sensitivity to Fas ligand (FasL) and expression level of decoy receptor 3 (DcR3) on tumor cell surface, Fas/DcR3 mRNA expression was detected by RT-PCR. Anti-DcR3 mAb was used to detect expression level of DcR3 on surface of tumor cells by flow cytometry. Caspase-8, caspase-9, caspase-3, Bcl-2 expressions were analyzed by Western blot, respectively. Sensitivity to apoptosis induced by FasL was determined by Annexin V apoptosis kit. The expressions of DcR3 on the surface of tumor cells from high to low were approximately 35.3% in BGC823 cells, and 21.6% in MCF-7 cells, respectively. The apoptotic rates induced by FasL from low to high were 15.6% in BGC823 cells, and 58.2% in MCF-7 cells, respectively. There was a significant correlation between the expression levels of DcR3 with FasL-inducing apoptosis.
机译:为了研究对Fas配体(FasL)的敏感性与肿瘤细胞表面诱饵受体3(DcR3)表达水平之间的相关性,通过RT-PCR检测Fas / DcR3 mRNA的表达。抗DcR3单克隆抗体用于通过流式细胞仪检测肿瘤细胞表面DcR3的表达水平。通过Western印迹分别分析了Caspase-8,caspase-9,caspase-3,Bcl-2的表达。用膜联蛋白V凋亡试剂盒测定对FasL诱导的凋亡的敏感性。 DcR3在肿瘤细胞表面的表达从高到低分别在BGC823细胞中约35.3%,在MCF-7细胞中约21.6%。 FasL从低到高诱导的凋亡率在BGC823细胞中分别为15.6%,在MCF-7细胞中为58.2%。 DcR3的表达水平与FasL诱导的细胞凋亡之间存在显着的相关性。

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