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蛋白质微阵列分析针对异种移植物释放蛋白的抗体产生可发现前列腺癌标志物。

Profiling of antibody production against xenograft-released proteins by protein microarrays discovers prostate cancer markers.

机构信息

Department of Urology, Erasmus MC , 3000 CA Rotterdam, The Netherlands.

出版信息

J Proteome Res. 2012 Feb 3;11(2):728-35. doi: 10.1021/pr2006473. Epub 2011 Dec 22.

Abstract

This study describes a novel xenograft-based biomarker discovery platform and proves its usefulness in the discovery of serum markers for prostate cancer. By immunizing immuno-competent mice with serum from nude mice bearing prostate cancer xenografts, an antibody response against xenograft-derived antigens was elicited. By probing protein microarrays with serum from immunized mice, several prostate cancer-derived antigens were identified, of which a subset was successfully retrieved in serum from mice bearing prostate cancer xenografts and prevalidated in human serum samples of prostate cancer patients. Among the discovered and validated proteins were the members of the TAM receptor family (TYRO3, AXL, and MERTK), ACY1, and PSMA1. In conclusion, this novel method allows for the identification of low abundant cancer-derived serum proteins, circumventing dynamic range and host-response issues in standard patient cohort proteomics comparisons.

摘要

本研究描述了一种新颖的基于异种移植物的生物标志物发现平台,并证明了其在发现前列腺癌的血清标志物方面的有用性。通过用携带前列腺癌异种移植物的裸鼠血清免疫免疫功能正常的小鼠,引发了针对异种移植物衍生抗原的抗体反应。通过用免疫小鼠的血清探测蛋白质微阵列,鉴定出了几种前列腺癌衍生抗原,其中一部分在携带前列腺癌异种移植物的小鼠的血清中成功回收,并在前列腺癌患者的人血清样本中进行了预验证。在发现和验证的蛋白质中包括 TAM 受体家族(TYRO3、AXL 和 MERTK)、ACY1 和 PSMA1 的成员。总之,这种新方法允许鉴定低丰度的癌症衍生血清蛋白,避免了标准患者队列蛋白质组学比较中动态范围和宿主反应问题。

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