Bioneer A/S , Hørsholm , Denmark.
Department of Pathology, Herlev Hospital, University of Copenhagen , Herlev , Denmark.
Front Oncol. 2014 Aug 15;4:207. doi: 10.3389/fonc.2014.00207. eCollection 2014.
Trastuzumab is established as standard care for patients with HER2-positive breast cancer both in the adjuvant and metastatic setting. However, 50% of the patients do not respond to the trastuzumab therapy, and therefore new predictive biomarkers are highly warranted. MicroRNAs (miRs) constitute a new group of biomarkers and their cellular expression can be determined in tumor samples by in situ hybridization (ISH) analysis. miR-21 is highly prevalent and up-regulated in breast cancer and has been linked to drug resistance in clinical and in vitro settings. To determine expression patterns of miR-21 in high-grade breast cancers, we examined miR-21 expression in 22 HER2-positive tumors and 15 HER2-negative high-grade tumors by ISH. The histological examination indicated that patient samples could be divided into three major expression patterns: miR-21 predominantly in tumor stroma, predominantly in cancer cells, or in both stromal and cancer cells. There was no obvious difference between the HER2-positive and HER2-negative tumors in terms of the miR-21 expression patterns and intensities. To explore the possibility that miR-21 expression levels and/or cellular localization could predict resistance to adjuvant trastuzumab in HER2-positive breast cancer patients, we analyzed additional 16 HER2-positive tumors from patients who were treated with trastuzumab in the adjuvant setting. Eight of the 16 patients showed clinical recurrence and were considered resistant. Examination of the miR-21 expression patterns and intensities revealed no association between the miR-21 scores in the cancer cell population (p = 0.69) or the stromal cells population (p = 0.13) and recurrent disease after adjuvant trastuzumab. Thus, our findings show that elevated miR-21 expression does not predict resistance to adjuvant trastuzumab.
曲妥珠单抗已被确立为 HER2 阳性乳腺癌患者的标准治疗方法,无论是在辅助治疗还是转移治疗中。然而,有 50%的患者对曲妥珠单抗治疗没有反应,因此急需新的预测生物标志物。microRNAs(miRs)是一组新的生物标志物,其细胞表达可以通过原位杂交(ISH)分析在肿瘤样本中确定。miR-21 在乳腺癌中高度普遍存在且上调,并且已经在临床和体外环境中与耐药性相关联。为了确定 miR-21 在高级别乳腺癌中的表达模式,我们通过 ISH 检查了 22 例 HER2 阳性肿瘤和 15 例 HER2 阴性高级别肿瘤中的 miR-21 表达。组织学检查表明,患者样本可以分为三种主要的表达模式:miR-21 主要在肿瘤基质中、主要在癌细胞中或在基质和癌细胞中都有表达。在 HER2 阳性和 HER2 阴性肿瘤之间,miR-21 的表达模式和强度没有明显差异。为了探索 miR-21 表达水平和/或细胞定位是否可能预测 HER2 阳性乳腺癌患者对辅助曲妥珠单抗的耐药性,我们分析了 16 例接受辅助曲妥珠单抗治疗的 HER2 阳性肿瘤患者的额外 16 例肿瘤。16 例患者中有 8 例出现临床复发,被认为是耐药的。miR-21 表达模式和强度的检查显示,癌细胞群体中的 miR-21 评分(p=0.69)或基质细胞群体中的 miR-21 评分(p=0.13)与辅助曲妥珠单抗治疗后的复发性疾病之间没有关联。因此,我们的研究结果表明,miR-21 的高表达并不能预测对辅助曲妥珠单抗的耐药性。