Iida Mari, Bahrar Harsh, Brand Toni M, Pearson Hannah E, Coan John P, Orbuch Rachel A, Flanigan Bailey G, Swick Adam D, Prabakaran Prashanth J, Lantto Johan, Horak Ivan D, Kragh Michael, Salgia Ravi, Kimple Randy J, Wheeler Deric L
Department of Human Oncology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin.
Department of Human Oncology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin. Radboud Department of Radiation Oncology, University Medical Centre Nijmegen, Nijmegen, the Netherlands.
Mol Cancer Ther. 2016 Sep;15(9):2175-86. doi: 10.1158/1535-7163.MCT-16-0012. Epub 2016 Jul 15.
Cetuximab, an antibody against the EGFR, has shown efficacy in treating head and neck squamous cell carcinoma (HNSCC), metastatic colorectal cancer, and non-small cell lung cancer (NSCLC). Despite the clinical success of cetuximab, many patients do not respond to cetuximab. Furthermore, virtually all patients who do initially respond become refractory, highlighting both intrinsic and acquired resistance to cetuximab as significant clinical problems. To understand mechanistically how cancerous cells acquire resistance, we previously developed models of acquired resistance using the H226 NSCLC and UM-SCC1 HNSCC cell lines. Cetuximab-resistant clones showed a robust upregulation and dependency on the HER family receptors EGFR, HER2, and HER3. Here, we examined pan-HER, a mixture of six antibodies targeting these receptors on cetuximab-resistant clones. In cells exhibiting acquired or intrinsic resistance to cetuximab, pan-HER treatment decreased all three receptors' protein levels and downstream activation of AKT and MAPK. This correlated with decreased cell proliferation in cetuximab-resistant clones. To determine whether pan-HER had a therapeutic benefit in vivo, we established de novo cetuximab-resistant mouse xenografts and treated resistant tumors with pan-HER. This regimen resulted in a superior growth delay of cetuximab-resistant xenografts compared with mice continued on cetuximab. Furthermore, intrinsically cetuximab-resistant HNSCC patient-derived xenograft tumors treated with pan-HER exhibited significant growth delay compared with vehicle/cetuximab controls. These results suggest that targeting multiple HER family receptors simultaneously with pan-HER is a promising treatment strategy for tumors displaying intrinsic or acquired resistance to cetuximab. Mol Cancer Ther; 15(9); 2175-86. ©2016 AACR.
西妥昔单抗是一种抗表皮生长因子受体(EGFR)的抗体,已显示出在治疗头颈部鳞状细胞癌(HNSCC)、转移性结直肠癌和非小细胞肺癌(NSCLC)方面的疗效。尽管西妥昔单抗取得了临床成功,但许多患者对其并无反应。此外,几乎所有最初有反应的患者都会产生耐药性,这凸显了西妥昔单抗的内在和获得性耐药性是重大的临床问题。为了从机制上理解癌细胞如何获得耐药性,我们之前使用H226非小细胞肺癌和UM-SCC1头颈部鳞状细胞癌细胞系建立了获得性耐药模型。西妥昔单抗耐药克隆显示出HER家族受体EGFR、HER2和HER3的强烈上调及依赖性。在此,我们检测了泛HER,这是一种针对这些受体的六种抗体的混合物,作用于西妥昔单抗耐药克隆。在对西妥昔单抗表现出获得性或内在耐药性的细胞中,泛HER治疗降低了所有三种受体的蛋白水平以及AKT和MAPK的下游激活。这与西妥昔单抗耐药克隆中细胞增殖的减少相关。为了确定泛HER在体内是否具有治疗益处,我们建立了新的西妥昔单抗耐药小鼠异种移植模型,并用泛HER治疗耐药肿瘤。与继续使用西妥昔单抗的小鼠相比,该方案导致西妥昔单抗耐药异种移植瘤的生长延迟更显著。此外,用泛HER治疗的内在西妥昔单抗耐药的头颈部鳞状细胞癌患者来源的异种移植瘤与载体/西妥昔单抗对照组相比,显示出显著的生长延迟。这些结果表明,用泛HER同时靶向多个HER家族受体是一种有前景的治疗策略,适用于对西妥昔单抗表现出内在或获得性耐药的肿瘤。《分子癌症治疗》;15(9);2175 - 86。©2016美国癌症研究协会。