首页> 外文期刊>American journal of clinical pathology. >Validation of a postfixation tissue storage and transport medium to preserve histopathology and molecular pathology analyses (total and phosphoactivated proteins, and FISH).
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Validation of a postfixation tissue storage and transport medium to preserve histopathology and molecular pathology analyses (total and phosphoactivated proteins, and FISH).

机译:固定后组织存储和运输介质的验证,以保存组织病理学和分子病理学分析(总蛋白和磷酸激活蛋白以及FISH)。

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摘要

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.
机译:肿瘤生物标志物研究是肿瘤学临床试验必不可少的,但由于样品获取和处理的差异,可能会产生人为的结果。使用PI3K / Akt / mTOR途径的标记物,以体积/体积计70%的乙醇作为样品传输介质进行了验证。切除BT474肿瘤异种移植物,并将切片立即置于甲醛中并固定24小时。立即将固定的组织切片加工成石蜡或转移至70%vol / vol乙醇中,并在室温下保存1、2和4周,然后再进行进一步处理。通过荧光原位杂交对鲜切的组织切片进行pAKT(S473),HER2,pHER-2(Y1248),pS6(S235 / 236)和pS6(S240 / 244),Ki-67和HER2的评估,并用H&E和Masson trichrome。将存储在70%乙醇中长达4周的样品与立即处理的组织进行比较,没有观察到显着变化。乙醇(体积/体积百分比为70%)为甲醛固定的肿瘤组织提供了安全的存储介质,有助于在多中心临床试验期间进行样品运输。

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