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微波辅助抗原修复后基底细胞皮肤癌中p53蛋白的免疫组织化学检测

Immunohistochemical detection of p53 protein in basal cell skin cancer after microwave-assisted antigen retrieval.

作者信息

Evke E, Minbay F Z, Temel S G, Kahveci Z

机构信息

Medical Genetics Department, Faculty of Medicine, Uludag University, Bursa, Turkey.

出版信息

J Mol Histol. 2009 Feb;40(1):13-21. doi: 10.1007/s10735-008-9208-8. Epub 2008 Dec 19.

Abstract

p53 is the most frequently altered tumor-suppressor gene in skin cancer. In normal tissues the p53 protein (wild type) has a very short half-life and it is not detectable immunohistochemically. In contrast, the mutant p53 protein has an extended half-life in tumor cells and can be detected by immunohistochemical methods. p53 is widely used as an indicator of tumor aggression and progression. Fixation methods especially formaldehyde based fixation may mask the immunohistochemical detection of p53 protein but antigen retrieval methods enhance the inmmunohistochemical detection of p53 protein by remodification of protein structure. This study was designed to evaluate the efficacy of different fixatives, of microwaving and microwave pretreatment method to retrieve p53 immunoreactivity in paraffin-embedded non-lesioned (adjacent normal tissue) human skin samples or pathological human skin samples diagnosed as basal cell carcinoma. The samples were fixed at RT and/or in microwave oven either in neutral buffered formalin or alcohol for different time periods. For antigen retrieval, the sections were irradiated in a microwave oven for 5 cycles in 10 mM citrate buffer (pH 6.00). In this study the effects of six different fixation methods on the immunohistochemical staining have been investigated in basal cell tumor specimens. The application of antigen retrieval method was also examined and compared. Optimal results were obtained using samples fixed in alcohol either at room temperature (24 h) or in microwave oven.

摘要

p53是皮肤癌中最常发生改变的肿瘤抑制基因。在正常组织中,p53蛋白(野生型)半衰期很短,免疫组化无法检测到。相反,突变型p53蛋白在肿瘤细胞中的半衰期延长,可通过免疫组化方法检测到。p53被广泛用作肿瘤侵袭和进展的指标。固定方法尤其是基于甲醛的固定可能会掩盖p53蛋白的免疫组化检测,但抗原修复方法通过重塑蛋白质结构增强了p53蛋白的免疫组化检测。本研究旨在评估不同固定剂、微波处理及微波预处理方法对石蜡包埋的非病变(相邻正常组织)人类皮肤样本或诊断为基底细胞癌的人类病理皮肤样本中p53免疫反应性的恢复效果。样本在室温下和/或在微波炉中用中性缓冲福尔马林或酒精固定不同时间段。为进行抗原修复,切片在10 mM柠檬酸盐缓冲液(pH 6.00)中于微波炉中照射5个循环。在本研究中,已在基底细胞瘤标本中研究了六种不同固定方法对免疫组化染色的影响。还对抗原修复方法的应用进行了检查和比较。使用在室温(24小时)或微波炉中用酒精固定的样本可获得最佳结果。

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