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一种人羧酸酯酶2剪接变体的表达与特性分析

Expression and characterization of a human carboxylesterase 2 splice variant.

作者信息

Schiel Marissa A, Green Scheri-lyn, Davis Wilhelmina I, Sanghani Paresh C, Bosron William F, Sanghani Sonal P

机构信息

Department of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, Indiana, USA.

出版信息

J Pharmacol Exp Ther. 2007 Oct;323(1):94-101. doi: 10.1124/jpet.107.127027. Epub 2007 Jul 17.

Abstract

CPT-11 [7-ethyl-10-[4-(1-piperidino)-1-piperidino] carbonyloxycamptothecin or Irinotecan] is a carbamate prodrug that is activated in vivo by carboxylesterase (CES)-2 to SN-38 (7-ethyl-10-hydroxycamptothecin), a potent topoisomerase I inhibitor. There is high interindividual variation when CPT-11 is used in the treatment of colorectal cancer. Several splice variants of CES2 are reported in the expressed sequence tag database. Real-time polymerase chain reaction was used to determine the abundance of the CES2 and splice variant of human carboxylesterase 2 (CES2Delta(458-473)) transcripts in 10 paired samples of human tumor and normal colon tissue. The results showed that the CES2Delta(458-473) transcript accounts for an average of 6% of total CES2 transcripts in colon tissue, and there is large interindividual variation in CES2 expression in both tumor and normal colon samples. The carboxylesterase activity of the colon samples was determined by 4-methylumbelliferyl acetate hydrolysis assays and nondenaturing polyacrylamide gel electrophoresis followed by activity staining. Significant, positive correlations were found between CES2 expression levels and both measures of carboxylesterase activity. We cloned and expressed the CES2Delta(458-473) protein in Sf9 insect cells. The purification profiles and preliminary characterization of the CES2Delta(458-473) protein indicated that the expressed protein is folded and glycosylated like CES2. However, in vitro assays show that the CES2Delta(458-473) protein lacks 4-methylumbelliferyl acetate and irinotecan hydrolase activities. In conclusion, we found that the CES2Delta(458-473) protein is an inactive splice variant of CES2 and that its transcript is spliced at a relatively constant rate in tumor and normal colon tissue.

摘要

CPT - 11[7 - 乙基 - 10 - [4 - (1 - 哌啶基) - 1 - 哌啶基]羰基氧喜树碱或伊立替康]是一种氨基甲酸酯前体药物,在体内由羧酸酯酶(CES)-2激活为SN - 38(7 - 乙基 - 10 - 羟基喜树碱),一种强效的拓扑异构酶I抑制剂。当CPT - 11用于治疗结直肠癌时,个体间存在很大差异。在表达序列标签数据库中报道了CES2的几种剪接变体。采用实时聚合酶链反应来测定10对人肿瘤和正常结肠组织样本中人类羧酸酯酶2(CES2)及其剪接变体(CES2Delta(458 - 473))转录本的丰度。结果显示,CES2Delta(458 - 473)转录本在结肠组织中平均占总CES2转录本的6%,并且在肿瘤和正常结肠样本中CES2表达存在很大的个体间差异。通过乙酸4 - 甲基伞形酮水解试验以及非变性聚丙烯酰胺凝胶电泳后进行活性染色来测定结肠样本的羧酸酯酶活性。发现CES2表达水平与两种羧酸酯酶活性测定结果之间存在显著的正相关。我们在Sf9昆虫细胞中克隆并表达了CES2Delta(458 - 473)蛋白。CES2Delta(458 - 473)蛋白的纯化图谱和初步表征表明,表达的蛋白像CES2一样折叠并进行了糖基化。然而,体外试验表明CES2Delta(458 - 473)蛋白缺乏乙酸4 - 甲基伞形酮和伊立替康水解酶活性。总之,我们发现CES2Delta(458 - 473)蛋白是CES2的一种无活性剪接变体,并且其转录本在肿瘤和正常结肠组织中以相对恒定的速率进行剪接。

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