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体外研究胞嘧啶脱氨酶-尿嘧啶磷酸核糖基转移酶介导的自杀基因治疗中的凋亡信号通路。

Understanding apoptotic signaling pathways in cytosine deaminase-uracil phosphoribosyl transferase-mediated suicide gene therapy in vitro.

作者信息

Gopinath P, Ghosh Siddhartha Sankar

机构信息

Department of Biotechnology, Centre for Nanotechnology, Indian Institute of Technology Guwahati, Guwahati, 781039, India.

出版信息

Mol Cell Biochem. 2009 Apr;324(1-2):21-9. doi: 10.1007/s11010-008-9980-5. Epub 2008 Dec 14.

Abstract

Cytosine deaminase-uracil phosphoribosyl transferase (CD-UPRT) fusion gene is known to exhibit therapeutic effect by inducing apoptosis in vitro. However, bystander effects of 5-flurocytosine (5-FC)/CD-UPRT and the molecular mechanism for apoptosis are yet to be established. In the present study, we have generated BHK21 cell line expressing both CD-UPRT and green fluorescent protein (GFP) from two separate transcripts, where GFP was used as a noninvasive probe to monitor the therapeutic effect of CD-UPRT. Enzyme activity of CD-UPRT in the stable cell line was measured by the reverse phase high-performance liquid chromatography analysis. Inhibition of cell growth and strong bystander effects of 5-FC/CD-UPRT were established, whereas characteristic surface morphology of apoptotic cell death was identified by AFM analysis. Involvement of various apoptotic signaling genes using semi-quantitative RT-PCR has been explored to substantiate the potential application of 5-FC/CD-UPRT suicide gene in therapy.

摘要

已知胞嘧啶脱氨酶-尿嘧啶磷酸核糖转移酶(CD-UPRT)融合基因在体外可通过诱导细胞凋亡发挥治疗作用。然而,5-氟胞嘧啶(5-FC)/CD-UPRT的旁观者效应以及细胞凋亡的分子机制尚未明确。在本研究中,我们从两个独立转录本构建了同时表达CD-UPRT和绿色荧光蛋白(GFP)的BHK21细胞系,其中GFP用作无创探针以监测CD-UPRT的治疗效果。通过反相高效液相色谱分析测定稳定细胞系中CD-UPRT的酶活性。确定了5-FC/CD-UPRT对细胞生长的抑制作用和强烈的旁观者效应,而通过原子力显微镜分析鉴定了凋亡细胞死亡的特征性表面形态。已利用半定量逆转录-聚合酶链反应探索各种凋亡信号基因的参与情况,以证实5-FC/CD-UPRT自杀基因在治疗中的潜在应用。

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