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探索尿液中 survivin 检测的固相邻近连接分析。

Exploring solid-phase proximity ligation assay for survivin detection in urine.

机构信息

Institute for Prevention and Occupational Medicine of the German Social Accident Insurance, Institute of the Ruhr-University Bochum (IPA), Bochum, Germany.

Department of Urology, HELIOS Hospital, Krefeld, Germany.

出版信息

PLoS One. 2022 Jun 29;17(6):e0270535. doi: 10.1371/journal.pone.0270535. eCollection 2022.

Abstract

Urine-based biomarkers are a rational and promising approach for the detection of bladder cancer due to the proximity of urine to the location of the tumor site and the non-invasive nature of its sampling. A well-known and highly investigated biomarker for bladder cancer is survivin. For detection of very small amounts of urinary survivin protein a highly sensitive assay was developed. The assay is based on the immuno-PCR technology, more precisely a solid-phase proximity ligation assay (spPLA). The limit of detection for the survivin spPLA was 1.45 pg/mL, resulting in an improvement of the limit of detection by a factor of approximately 23 compared to the previously in-house developed survivin ELISA. A key step in development was the initial isolation of survivin by a molecular fishing rod based on magnetic beads. Interfering matrix compounds pose a special challenge for further analytical application, but can be overcome by this isolation step. The assay is designed to work with only 500 μL of voided urine. The survivin spPLA showed a sensitivity of 30% and specificity of 89% for bladder cancer detection in this study of 110 bladder cancer cases and 133 clinical controls. Moreover, the results demonstrated again that survivin is a useful complementary marker in combination with UBC® Rapid by increasing the overall sensitivity to 70% with a specificity of 86%. Although the performance for detection of bladder cancer was rather low, the herein developed assay might serve as a new tool for survivin biomarker research in diverse human fluids, even if the biological matrix is complex or survivin is only present in small amounts.

摘要

基于尿液的生物标志物是检测膀胱癌的一种合理且有前途的方法,因为尿液与肿瘤部位接近,且其采样具有非侵入性。生存素是膀胱癌的一种众所周知且高度研究的生物标志物。为了检测非常少量的尿液生存素蛋白,开发了一种高度敏感的测定法。该测定法基于免疫-PCR 技术,更确切地说是固相邻近连接测定法(spPLA)。生存素 spPLA 的检测限为 1.45pg/mL,与之前内部开发的生存素 ELISA 相比,检测限提高了约 23 倍。开发过程中的一个关键步骤是最初通过基于磁珠的分子钓竿分离生存素。干扰基质化合物对进一步的分析应用构成了特殊挑战,但可以通过这种分离步骤克服。该测定法旨在仅使用 500μL 的排空尿液工作。在这项对 110 例膀胱癌病例和 133 例临床对照的研究中,生存素 spPLA 对膀胱癌检测的灵敏度为 30%,特异性为 89%。此外,结果再次表明,生存素与 UBC® Rapid 联合使用是一种有用的互补标志物,可将总体灵敏度提高到 70%,特异性为 86%。尽管膀胱癌检测的性能相当低,但在此开发的测定法可能成为不同人体液中生存素生物标志物研究的新工具,即使生物基质复杂或生存素仅以少量存在。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5af5/9242480/454ed79bdb69/pone.0270535.g001.jpg

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