摘要
引入曲妥珠单抗的抗HER2治疗可以明显改变HER2阳性乳腺癌病人的临床效果。采用原发性肿瘤中HER2表达/扩增状态来选择符合曲妥珠单抗的病人。然而,对这些病人的抗HER2治疗获得性和内在抵抗力表现了重大挑战性,需要较好的临床分层来改善临床反应。 在此,我们提供了潜在标志物针对病人对曲妥珠反应的分层能力的广泛综述。包括HER2扩增,修复通往结合位点(p95HER2, Δ16HER-2, MUC4),通过其他ERBB家族受体(HER1, HER3, HER4)和他们的配体增强的通路,可替代的异二聚体HER2活性靶点,下游基因引起的信号(PIK3CA, PTEN, SRC, mTOR),细胞周期和凋亡调节因子的异常表达(CDKs, p27kip1, Bcl-2),激素受体状态,抗体依赖细胞介导的细胞毒作用(FcγR),以及miRNA异常表达特征。
关键词: 乳腺癌,二聚作用,人类表皮生长因子受体,分子亚型,阴性预测标记物,存活,曲妥珠单抗,肿瘤异质性
图形摘要
Current Cancer Drug Targets
Title:A Comprehensive Outline of Trastuzumab Resistance Biomarkers in HER2 Overexpressing Breast Cancer
Volume: 15 Issue: 8
Author(s): Otília Menyhart, Libero Santarpia and Balazs Gyorffy
Affiliation:
关键词: 乳腺癌,二聚作用,人类表皮生长因子受体,分子亚型,阴性预测标记物,存活,曲妥珠单抗,肿瘤异质性
摘要: The introduction of trastuzumab for anti-HER2 therapy dramatically changed the clinical outcome for HER2 (ERBB2, neu) positive breast cancer patients. Today, patients eligible for trastuzumab are selected using HER2 expression/amplification status of the primary tumor. However, acquired and inherent resistance to anti-HER2 therapy in these patients poses a significant challenge, and better patient stratification will be needed to improve clinical response.
Here, we provide a wide-ranging overview of potential biomarkers capable of stratifying patients regarding their response to trastuzumab. These include HER2 amplification, impaired access to the binding site (p95HER2, Δ16HER-2, MUC4), augmented signaling through other ERBB family receptors (HER1, HER3, HER4) and their ligands, activation of HER2 targets by alternate heterodimers (EphA2, IGF-1R, GDF15, MUC1*), signaling triggered by downstream members (PIK3CA, PTEN, SRC, mTOR), altered expression of cell cycle and apoptotic regulators (CDKs, p27kip1, Bcl-2), hormone receptor status, resistance to antibody-dependent cellular cytotoxicity (FcγR), and altered miRNA expression signatures.
Multigenic molecular profile analyses have revealed further genes not directly associated with classical oncogenic pathways. Although numerous biomarkers have shown promise in pre-clinical studies, many have delivered controversial results when evaluated in clinical trials. One of the keys for targeting ERBB2 will be to consider the entire ERBB family and downstream associated pathways responsible for the malignant transformation.
The heterogeneity of the disease is likely to represent a significant obstacle to accurately predicting the course of resistance. The future most probably involves the incorporation of multiple biomarkers into a unified predictor enabling selection of patients for superior targeted drug administration.
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Otília Menyhart, Libero Santarpia and Balazs Gyorffy , A Comprehensive Outline of Trastuzumab Resistance Biomarkers in HER2 Overexpressing Breast Cancer, Current Cancer Drug Targets 2015; 15 (8) . https://dx.doi.org/10.2174/156800961508151001101742
DOI https://dx.doi.org/10.2174/156800961508151001101742 |
Print ISSN 1568-0096 |
Publisher Name Bentham Science Publisher |
Online ISSN 1873-5576 |
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