Somers Gino R, Ho Michael, Zielenska Maria, Squire Jeremy A, Thorner Paul S
Department of Pediatric Laboratory Medicine, Hospital for Sick Children, 555 University Avenue, Toronto, ON, M5G 1X8, Canada.
Pediatr Dev Pathol. 2005 Sep-Oct;8(5):525-32. doi: 10.1007/s10024-005-0044-5. Epub 2005 Oct 5.
The HER2 gene, located on 17q, encodes a 185-kD transmembrane tyrosine kinase receptor. Amplification of this gene with overexpression of the gene product occurs in about 30% of cases of breast cancer and is considered to be a poor prognostic indicator for this tumor. Results for HER2 expression in osteosarcoma are controversial, with some studies reporting up to 61% of positive cases and others reporting only negative results. Further, expression of HER2 is reported to be a favorable prognostic indicator by some groups and unfavorable by others. The present study used tissue microarrays containing 34 samples of osteosarcoma from 18 patients to analyze HER2 expression by immunohistochemistry and gene copy number by chromogenic in situ hybridization. The microarray included 13 pretreatment biopsies, 11 posttreatment resection specimens, and 10 resected metastases and comprised 18 osteoblastic, 6 chondroblastic, 5 fibroblastic, and 5 mixed subtypes. HER2 protein expression was seen in 4 of 34 (12%) tumor samples that originated from 2 of 18 patients (11%). The staining pattern was consistently weak and focal, and immunohistochemical overexpression of the HER2 protein, defined as complete membrane positivity, was never observed. Further, the presence of HER2 gene amplification was not detected in any osteosarcoma by chromogenic in situ hybridization. Therefore, therapies based on antibodies directed against the HER2 protein are unlikely to have much value in the treatment of pediatric osteosarcomas. From a technical standpoint, this study also demonstrates the value of tissue microarrays in screening tumors at the protein and gene levels using conventional light microscopy.
HER2基因位于17号染色体长臂,编码一种185-kD的跨膜酪氨酸激酶受体。该基因的扩增及基因产物的过表达发生在约30%的乳腺癌病例中,被认为是该肿瘤预后不良的指标。骨肉瘤中HER2表达的结果存在争议,一些研究报告阳性病例高达61%,而另一些研究仅报告阴性结果。此外,一些研究组报告HER2表达是一个有利的预后指标,而另一些研究组则认为是不利的。本研究使用包含18例患者的34个骨肉瘤样本的组织芯片,通过免疫组织化学分析HER2表达,并通过显色原位杂交分析基因拷贝数。该芯片包括13个治疗前活检样本、11个治疗后切除标本和10个切除转移灶,包含18个成骨细胞型、6个软骨母细胞型、5个纤维母细胞型和5个混合型亚型。在34个肿瘤样本中的4个(12%)检测到HER2蛋白表达,这些样本来自18例患者中的2例(11%)。染色模式始终较弱且呈局灶性,从未观察到HER2蛋白免疫组化过表达(定义为完全膜阳性)。此外,通过显色原位杂交在任何骨肉瘤中均未检测到HER2基因扩增。因此,基于抗HER2蛋白抗体的治疗方法在小儿骨肉瘤治疗中不太可能有太大价值。从技术角度来看,本研究还证明了组织芯片在使用传统光学显微镜在蛋白质和基因水平筛选肿瘤方面的价值。