Gancberg D, Lespagnard L, Rouas G, Paesmans M, Piccart M, Di Leo A, Nogaret J M, Hertens D, Verhest A, Larsimont D
Department of Pathology, Institut Jules Bordet, Brussels, Belgium.
Am J Clin Pathol. 2000 May;113(5):675-82. doi: 10.1309/0F58-0GRX-FK4R-A6VA.
Overexpression and amplification of the HER-2 oncogene in patients with breast cancer has correlated with early onset of metastasis, resistance to hormonal therapy and some forms of chemotherapy, and shortened survival. Therefore, evaluation of this putative prognostic or predictive factor seems critical. Because different antibodies are used for the detection of the 185-kd HER-2 oncoprotein, we studied the sensitivity of 3 frequently used antibodies. Immunohistochemistry results were correlated with gene amplification level as assessed by fluorescence in situ hybridization. Protein overexpression was found in 17.2% and 12.5% of cases using antibodies against the external (TAB250) and internal (CB11) domains of the protein, respectively, and in 38.0% of cases using a rabbit polyclonal antibody. Fluorescence in situ hybridization was successful in all 160 tumors, and amplification was found in 37 tumors (23.1%). The monoclonal antibody TAB250 had the lowest misclassification rate, 9.6% (sensitivity, 67%; specificity, 97.5%).
乳腺癌患者中HER-2癌基因的过表达和扩增与转移的早期发生、对激素治疗及某些形式化疗的耐药性以及生存期缩短相关。因此,评估这个假定的预后或预测因素似乎至关重要。由于检测185-kd HER-2癌蛋白使用了不同的抗体,我们研究了3种常用抗体的敏感性。免疫组织化学结果与通过荧光原位杂交评估的基因扩增水平相关。分别使用针对该蛋白外部(TAB250)和内部(CB11)结构域的抗体时,在17.2%和12.5%的病例中发现了蛋白过表达,而使用兔多克隆抗体时在38.0%的病例中发现了蛋白过表达。荧光原位杂交在所有160个肿瘤中均成功进行,在37个肿瘤(23.1%)中发现了扩增。单克隆抗体TAB250的错误分类率最低,为9.6%(敏感性为67%;特异性为97.5%)。