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胚胎型横纹肌肉瘤中 ERBB2(HER2)扩增:罕见病例中的潜在治疗靶点?

英文原题:Amplification of ERBB2 (HER2) in embryonal rhabdomyosarcoma: A potential treatment target in rare cases?

PubMed 2021/09/01(内容时间) Genes Chromosomes Cancer Q3 · IF 2.3(JCR 2025)

研究概要

ERBB2 基因编码一种受体酪氨酸激酶,也称为 HER2。

中文摘要

ERBB2基因编码一种受体酪氨酸激酶,也称HER2。约五分之一乳腺癌存在ERBB2扩增并过表达;此类肿瘤患者可从曲妥珠单抗或其他阻断该受体的药物中获益。此外,其他多种恶性肿瘤也可出现ERBB2扩增和/或过表达。值得注意的是,肺泡型和胚胎型横纹肌肉瘤(RMS)尤其是儿童患者,常出现ERBB2表达升高。虽然RMS中尚未描述该基因的高水平扩增,但RMS细胞表面常见ERBB2表达,已被用于设计CAR-T 细胞(CAR T)治疗策略。本文报告2例儿童融合基因阴性的胚胎型RMS,均存在ERBB2基因高水平扩增。其中1例患者因近期发现的标准风险RMS接受常规化疗,另一例因转移性疾病死亡。两例肿瘤的17q12染色体区均存在局灶性扩增子,长度分别为210 kb和274 kb,其近端和远端边界与乳腺癌中常见的边界相对应;两例中ERBB2扩增均与RNA和蛋白质水平高表达相关。因此,类似乳腺癌的ERBB2扩增虽在儿童RMS中极为罕见,但会反复出现,应将其作为替代治疗靶点加以利用。

展开英文摘要原文

The ERBB2 gene encodes a receptor tyrosine kinase also known as HER2. The gene is amplified and overexpressed in one-fifth of breast carcinomas; patients with such tumors benefit from targeted treatment with trastuzumab or other drugs blocking the receptor. In addition, ERBB2 has been shown to be amplified and/or overexpressed in a variety of other malignancies. Notably, both alveolar and embryonal rhabdomyosarcoma (RMS), especially in children, often show increased expression of ERBB2. Although high-level amplification of the gene has not been described in RMS, its frequent expression at the cell surface of RMS cells has been exploited for chimeric antigen receptor T-cell (CAR T)-based treatment strategies. We here describe two cases of pediatric, fusion-negative embryonal RMS with high-level amplification of the ERBB2 gene. One patient is currently treated with conventional chemotherapy for a recently detected standard risk RMS, whereas the other patient died from metastatic disease. Both tumors displayed focal amplicons (210 and 274 Kb, respectively) in chromosome band 17q12, with proximal and distal borders corresponding to those typically seen in breast cancer. In both tumors, the ERBB2 amplicon correlated with high expression at the RNA and protein levels. Thus, breast cancer-like ERBB2 amplification is a very rare, but recurrent feature of pediatric RMS, and should be exploited as an alternative treatment target.

论文信息

作者
Mitra S、Sydow S、Magnusson L、Piccinelli P、Törnudd L、Øra I、Ljungman G、Sandgren J
单位
Department of Laboratory Medicine, Division of Clinical Genetics, Lund University, Lund, Sweden.Sweden
文献类型
病例报告 · 非美国政府资助研究
期刊
Genes, chromosomes & cancer2022 Jan
原文标识
PubMed 34418214 · DOI 10.1002/gcc.22996