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采用 iTRAQ 标记、二维液相色谱和串联质谱技术对福尔马林固定石蜡包埋的鼻咽癌进行定量蛋白质组学分析。

Quantitative proteomic analysis of formalin-fixed and paraffin-embedded nasopharyngeal carcinoma using iTRAQ labeling, two-dimensional liquid chromatography, and tandem mass spectrometry.

机构信息

Key Laboratory of Cancer Proteomics of Chinese Ministry of Health, Xiangya Hospital, Central South University, 87# Xiangya Road, Changsha 410008, Hunan, China.

出版信息

J Histochem Cytochem. 2010 Jun;58(6):517-27. doi: 10.1369/jhc.2010.955526. Epub 2010 Feb 1.

DOI:10.1369/jhc.2010.955526
PMID:20124091
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2874184/
Abstract

Formalin-fixed, paraffin-embedded (FFPE) tissue specimens represent a potentially valuable resource for protein biomarker investigations. In this study, proteins were extracted by a heat-induced antigen retrieval technique combined with a retrieval solution containing 2% SDS from FFPE tissues of normal nasopharyngeal epithelial tissues (NNET) and three histological types of nasopharyngeal carcinoma (NPC) with diverse differentiation degrees. Then two-dimensional liquid chromatography-tandem mass spectrometry coupled with isobaric tags for relative and absolute quantification (iTRAQ) labeling was employed to quantitatively identify the differentially expressed proteins among the types of NPC FFPE tissues. Our study resulted in the identification of 730 unique proteins, the distributions of subcellular localizations and molecular functions of which were similar to those of the proteomic database of human NPC and NNET that we had set up based on the frozen tissues. Additionally, the relative expression levels of cathepsin D, keratin8, SFN, and stathmin1 identified and quantified in this report were consistent with the immunohistochemistry results acquired in our previous study. In conclusion, we have developed an effective approach to identifying protein changes in FFPE NPC tissues utilizing iTRAQ technology in conjunction with an economical and easily accessible sample preparation method.

摘要

福尔马林固定、石蜡包埋(FFPE)组织标本代表了一种潜在有价值的蛋白质生物标志物研究资源。在本研究中,我们采用一种热诱导抗原修复技术,并结合含有 2% SDS 的修复液从正常鼻咽上皮组织(NNET)和三种具有不同分化程度的鼻咽癌(NPC)的 FFPE 组织中提取蛋白质。然后,我们采用二维液相色谱-串联质谱技术结合相对和绝对定量同位素标记(iTRAQ)标记,定量鉴定 NPC FFPE 组织类型之间的差异表达蛋白。我们的研究共鉴定到 730 种独特蛋白,这些蛋白的亚细胞定位和分子功能分布与我们基于冷冻组织建立的人类 NPC 和 NNET 蛋白质组数据库中的蛋白相似。此外,本报告中鉴定和定量的组织蛋白酶 D、角蛋白 8、SFN 和 stathmin1 的相对表达水平与我们之前研究中获得的免疫组织化学结果一致。总之,我们已经开发出一种有效的方法,利用 iTRAQ 技术结合经济且易于获取的样品制备方法,来鉴定 FFPE NPC 组织中的蛋白变化。

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