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用于治疗诊断和患者个性化治疗的反相蛋白质微阵列。

Reverse-phase protein microarrays for theranostics and patient tailored therapy.

作者信息

Espina Virginia, Liotta Lance A, Petricoin Emanuel F

机构信息

Center for Applied Proteomics and Molecular Medicine, George Mason University, Manassas, VA, USA.

出版信息

Methods Mol Biol. 2009;520:89-105. doi: 10.1007/978-1-60327-811-9_7.

Abstract

Analysis of the genome provides important information about the somatic genetic changes existing in the tissue; however, it is the proteins that do the work of the cell. Diseases such as cancer are caused by derangements in cellular protein molecular networks and cell signaling pathways. These pathways contain a large and growing collection drug targets, governing cellular survival, proliferation, invasion, and cell death. The clinical utility of reverse-phase protein microarrays (RPPA), a new technology invented in our laboratory, lies in its ability to generate a functional map of known cell signaling networks or pathways for an individual patient obtained directly from a biopsy specimen. Coupled with laser capture microdissection (LCM), the RPPA platform, the entire cellular proteome is immobilized on a substratum with subsequent immunodetection of the total levels and phosphorylated, or activated, state of cell signaling proteins. The results of which pathways are "in use" can then be correlated with biological and clinical information and serve as both a diagnostic and a therapeutic guide, thus providing a "theranostic" endpoint.

摘要

基因组分析可提供有关组织中存在的体细胞遗传变化的重要信息;然而,执行细胞功能的是蛋白质。诸如癌症之类的疾病是由细胞蛋白质分子网络和细胞信号通路紊乱引起的。这些通路包含大量且不断增加的药物靶点,控制着细胞的存活、增殖、侵袭和细胞死亡。我们实验室发明的一项新技术——反相蛋白质微阵列(RPPA),其临床效用在于能够为直接从活检标本获取的个体患者生成已知细胞信号网络或通路的功能图谱。结合激光捕获显微切割(LCM),RPPA平台可将整个细胞蛋白质组固定在基质上,随后对细胞信号蛋白的总水平以及磷酸化或激活状态进行免疫检测。然后,哪些通路“正在发挥作用”的结果可与生物学和临床信息相关联,并用作诊断和治疗指南,从而提供一个“治疗诊断”终点。

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