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HER2Amplification and Overexpression Is Not Present in Pediatric Osteosarcoma: A Tissue Microarray Study

组织微阵列 骨肉瘤 免疫组织化学 显色原位杂交 荧光原位杂交 基因复制 病理 原位杂交 癌症 生物 乳腺癌 癌症研究 基因表达 微阵列 基因 DNA微阵列 分子生物学 医学 染色体 遗传学
作者
Gino R. Somers,Michael Ho,Maria Zieleńska,Jeremy A. Squire,Paul S. Thorner
出处
期刊:Pediatric and Developmental Pathology [SAGE Publishing]
卷期号:8 (5): 525-532 被引量:50
标识
DOI:10.1007/s10024-005-0044-5
摘要

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 micro-arrays in screening tumors at the protein and gene levels using conventional light microscopy.
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