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验证一种后置组织储存和运输介质,以保存组织病理学和分子病理学分析(总蛋白和磷酸化蛋白,以及 FISH)。

Validation of a postfixation tissue storage and transport medium to preserve histopathology and molecular pathology analyses (total and phosphoactivated proteins, and FISH).

机构信息

Oncology Research, Novartis Institutes of Biomedical Research, Novartis Pharma AG, Basel, Switzerland.

出版信息

Am J Clin Pathol. 2012 Mar;137(3):429-36. doi: 10.1309/AJCPDZ4FAQ9BUEXC.

Abstract

Tumor biomarker studies are integral to oncology clinical trials but may yield artifactual results owing to variation in sample procurement and processing. Ethanol, 70% vol/vol, was validated as a sample transport medium using markers of the PI3K/Akt/mTOR pathway. BT474 tumor xenografts were excised and slices were immediately placed into formaldehyde and fixed for 24 hours. Fixed tissue slices were immediately processed into paraffin or transferred to 70% vol/vol ethanol and stored at room temperature for 1, 2, and 4 weeks before further processing. Freshly cut tissue sections were evaluated for pAKT(S473), HER2, pHER-2(Y1248), pS6(S235/236), and pS6(S240/244), Ki-67, and HER2 by fluorescence in situ hybridization and stained with H&E and Masson trichrome. No significant changes were observed when comparing samples stored in 70% ethanol for up to 4 weeks with immediately processed tissue. Ethanol, 70% vol/vol, provides a safe storage medium for formaldehyde-fixed tumor tissue, facilitating sample transport during multicenter clinical trials.

摘要

肿瘤标志物研究是肿瘤临床试验的重要组成部分,但由于样本采集和处理的差异,可能会产生人为的结果。70%乙醇被验证为一种可用于 PI3K/Akt/mTOR 通路标志物的样本运输介质。BT474 肿瘤异种移植物被切除,组织切片立即放入甲醛中固定 24 小时。固定的组织切片立即加工成石蜡,或转移到 70%乙醇中,在室温下储存 1、2 和 4 周,然后再进一步处理。新鲜切割的组织切片通过荧光原位杂交评估 pAKT(S473)、HER2、pHER-2(Y1248)、pS6(S235/236)、pS6(S240/244)、Ki-67 和 HER2,并通过 H&E 和 Masson 三色染色进行染色。在比较在 70%乙醇中储存长达 4 周的样本与立即处理的组织时,未观察到明显变化。70%乙醇为福尔马林固定的肿瘤组织提供了一种安全的储存介质,便于在多中心临床试验中进行样本运输。

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