Strehl Johanna D, Hoegel Josef, Hornicek Ines, Hartmann Arndt, Riener Marc-Oliver
Institute of Pathology, University Hospital Erlangen-Nuremberg 91054 Erlangen, Germany.
Institute of Human Genetics, University Hospital Ulm 89081 Ulm, Germany.
Int J Clin Exp Pathol. 2014 Apr 15;7(5):2091-101. eCollection 2014.
Expression of the oncofetal protein insulin like growth factor II messenger ribonucleic acid binding protein 3 (IMP3) has been shown to differentiate between benign and malignant lesions in several tissues. Our aim was to assess the immunohistochemical expression of IMP3 in inflammatory and neoplastic lesions of the gastric mucosa and to determine whether IMP3, alone or in combination with p53, could be used for identifying neoplasia of the gastric mucosa.
IMP3 and p53 immunohistochemistry was performed on 57 cases of gastritis, 28 cases of dysplasia of the gastric mucosa and 63 cases of gastric carcinomas. Focal IMP3 positivity was detected in 86% of non-neoplastic lesions of the gastric mucosa. Using a simple product score (PS), 96% of non-neoplastic lesions of the gastric mucosa were assessed as IMP3(PS) negative. None of the low-grade dysplasia but 83% of high-grade dysplasia were IMP3(PS) positive. Gastric carcinomas showed IMP3(PS) positivity in 65%. Adding p53 to the diagnostic panel increased sensitivity significantly.
High-grade dysplasia and gastric carcinomas can be distinguished from low-grade dysplasia and inflammatory lesions of the gastric mucosa with a high specificity and good sensitivity using a combination of the immunohistochemical markers IMP3 and p53.
癌胚蛋白胰岛素样生长因子II信使核糖核酸结合蛋白3(IMP3)的表达已被证实在多种组织中可区分良性和恶性病变。我们的目的是评估IMP3在胃黏膜炎症性和肿瘤性病变中的免疫组化表达,并确定IMP3单独或与p53联合是否可用于识别胃黏膜肿瘤。
对57例胃炎、28例胃黏膜发育异常和63例胃癌进行IMP3和p53免疫组化检测。在86%的胃黏膜非肿瘤性病变中检测到IMP3局灶性阳性。使用简单乘积评分(PS),96%的胃黏膜非肿瘤性病变被评估为IMP3(PS)阴性。低级别发育异常中无一例IMP3(PS)阳性,但高级别发育异常中有83%为IMP3(PS)阳性。65%的胃癌显示IMP3(PS)阳性。将p53添加到诊断指标中可显著提高敏感性。
联合使用免疫组化标志物IMP3和p53,可高特异性和良好敏感性地将高级别发育异常和胃癌与胃黏膜低级别发育异常及炎症性病变区分开来。