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重新审视肿瘤生物标志物检测的技术验证:如何打开潘多拉的盒子。

Revisiting the technical validation of tumour biomarker assays: how to open a Pandora's box.

机构信息

Department of Biomedical Sciences and Human Oncology, University of Turin, Via Santena 7, 10126 Turin, Italy.

出版信息

BMC Med. 2011 Apr 19;9:41. doi: 10.1186/1741-7015-9-41.

Abstract

A tumour biomarker is a characteristic that is objectively measured and evaluated in tumour samples as an indicator of normal biological processes, pathogenic processes, or pharmacologic responses to a therapeutic intervention. The development of a biomarker contemplates distinct phases, including discovery by hypothesis-generating preclinical or exploratory studies, development and qualification of the assay for the identification of the biomarker in clinical samples, and validation of its clinical significance. Although guidelines for the development and validation of biomarkers are available, their implementation is challenging, owing to the diversity of biomarkers being developed. The term 'validation' undoubtedly has several meanings; however, in the context of biomarker research, a test may be considered valid if it is 'fit for purpose'. In the process of validation of a biomarker assay, a key point is the validation of the methodology. Here we discuss the challenges for the technical validation of immunohistochemical and gene expression assays to detect tumour biomarkers and provide suggestions of pragmatic solutions to address these challenges.

摘要

肿瘤标志物是在肿瘤样本中客观测量和评估的特征,可作为正常生物过程、病理过程或治疗干预的药理反应的指标。生物标志物的开发考虑了不同的阶段,包括通过假设生成的临床前或探索性研究进行发现、开发和鉴定用于鉴定临床样本中生物标志物的检测方法,以及验证其临床意义。尽管有用于生物标志物开发和验证的指南,但由于正在开发的生物标志物的多样性,其实施具有挑战性。术语“验证”无疑有几种含义;然而,在生物标志物研究的背景下,如果测试“适合目的”,则可以认为该测试是有效的。在生物标志物测定的验证过程中,关键点是验证方法。在这里,我们讨论了用于检测肿瘤标志物的免疫组织化学和基因表达测定的技术验证所面临的挑战,并提供了实用解决方案来解决这些挑战的建议。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1612/3102629/0b3c8444dd1a/1741-7015-9-41-1.jpg

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