ELISA检测前列腺癌患者血清中肿瘤蛋白53诱导核蛋白1的建立

Houda Saadi , Marion Seillier , Maria José Sandi , Sylvain Peuget , Christine Kellenberger , Gwenaëlle Gravis , Nelson J. Dusetti , Juan L. Iovanna , Palma Rocchi , Mohamed Amri , Alice Carrier
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引用次数: 5

摘要

肿瘤蛋白53诱导核蛋白1 (TP53INP1)在细胞应激反应中与强效的“基因组守护者”p53协同发挥重要作用。在人类中,编码TP53INP1的基因在一些病理情况下,如炎症和前列腺癌(PC)中表达非常高。TP53INP1在PC中的过表达似乎是一个较差的预后因素,特别是预测生物癌症复发,使TP53INP1成为阉割耐药(CR) PC分子治疗的相关特异性靶点。在这种情况下,检测患者生物体液中的TP53INP1是一种很有前途的诊断途径。我们在此报告成功开发了一种新的酶联免疫吸附法(ELISA)检测TP53INP1,利用分子工具(单克隆抗体(mab)和重组蛋白)在实验室中产生的基本功能研究过程中专门用于TP53INP1。ELISA原理基于夹心免疫酶系统,TP53INP1蛋白被包被在微孔板上的第一个特异性单抗捕获,然后被第二个特异性单抗识别。这种新的检测方法可以在几种PC患者的血清中特异性检测TP53INP1。这一突破为研究大队列患者和评估TP53INP1剂量的临床应用铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of an ELISA detecting Tumor Protein 53-Induced Nuclear Protein 1 in serum of prostate cancer patients

Tumor Protein 53-Induced Nuclear Protein 1 (TP53INP1) plays an important role during cell stress response in synergy with the potent “genome-keeper” p53. In human, the gene encoding TP53INP1 is expressed at very high level in some pathological situations, such as inflammation and prostate cancer (PC). TP53INP1 overexpression in PC seems to be a worse prognostic factor, particularly predictive of biological cancer relapse, making TP53INP1 a relevant specific target for molecular therapy of Castration Resistant (CR) PC. In that context, detection of TP53INP1 in patient biological fluids is a promising diagnostic avenue. We report here successful development of a new Enzyme-Linked Immunosorbent Assay (ELISA) detecting TP53INP1, taking advantage of molecular tools (monoclonal antibodies (mAbs) and recombinant proteins) generated in the laboratory during the course of basic functional investigations devoted to TP53INP1. The ELISA principle is based on a sandwich immunoenzymatic system, TP53INP1 protein being trapped by a first specific mAb coated on microplate then recognized by a second specific mAb. This new assay allows specific detection of TP53INP1 in serum of several PC patients. This breakthrough paves the way towards investigation of a large cohort of patients and assessment of clinical applications of TP53INP1 dosage.

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