Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.
University of Chinese Academy of Sciences, Beijing, China.
Cancer Sci. 2019 Nov;110(11):3584-3594. doi: 10.1111/cas.14180. Epub 2019 Sep 9.
Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKI) have been used as the first-line treatment of non-small cell lung cancers (NSCLC) harboring EGFR-activating mutations, but acquired resistance is ubiquitous and needs to be solved urgently. Here, we introduce an effective approach for overcoming resistance to the EGFR-TKI, AZD9291, in NSCLC cells using SHR-A1403, a novel c-mesenchymal-epithelial transition factor (c-Met)-targeting antibody-drug conjugate (ADC) consisting of an anti-c-Met monoclonal antibody (c-Met mAb) conjugated to a microtubule inhibitor. Resistant cells were established by exposing HCC827 to increasing concentrations of EGFR-TKI. c-Met was found to be overexpressed in most resistant cells. AZD9291 resistance was partially restored by combination of AZD9291 and crizotinib only in resistant cells overexpressing phospho-c-Met, which synergistically inhibited c-Met-mediated phosphorylation of the downstream targets ERK1/2 and AKT. In resistant cells overexpressing c-Met, neither crizotinib nor c-Met mAb was able to overcome AZD9291 resistance. In contrast, SHR-A1403 strongly inhibited proliferation of AZD9291-resistant HCC827 overexpressing c-Met, regardless of the levels of c-Met phosphorylation. SHR-A1403 bound to resistant cells overexpressing c-Met was internalized into cells and released associated microtubule inhibitor, resulting in cell-killing activity that was dependent on c-Met expression levels only, irrespective of the involvement of c-Met or EGFR signaling in AZD9291 resistance. Consistent with its activity in vitro, SHR-A1403 significantly inhibited the growth of AZD9291-resistant HCC827 tumors and caused tumor regression in vivo. Thus, our findings show that SHR-A1403 efficiently overcomes AZD9291 resistance in cells overexpressing c-Met, and further indicate that c-Met expression level is a biomarker predictive of SHR-A1403 efficacy.
表皮生长因子受体(EGFR)酪氨酸激酶抑制剂(TKI)已被用作携带 EGFR 激活突变的非小细胞肺癌(NSCLC)的一线治疗药物,但获得性耐药是普遍存在的,需要迫切解决。在这里,我们介绍了一种克服 EGFR-TKI,AZD9291,在 NSCLC 细胞中耐药性的有效方法,使用 SHR-A1403,一种由抗 c-Met 单克隆抗体(c-Met mAb)与微管抑制剂偶联而成的新型 c-间质上皮转化因子(c-Met)靶向抗体药物偶联物(ADC)。通过将 HCC827 暴露于不断增加的 EGFR-TKI 浓度来建立耐药细胞。发现大多数耐药细胞中 c-Met 过表达。仅在过表达磷酸化 c-Met 的耐药细胞中,AZD9291 与克唑替尼联合使用部分恢复了 AZD9291 耐药性,这协同抑制了 c-Met 介导的下游靶点 ERK1/2 和 AKT 的磷酸化。在过表达 c-Met 的耐药细胞中,克唑替尼或 c-Met mAb 均无法克服 AZD9291 耐药性。相比之下,SHR-A1403 强烈抑制过表达 c-Met 的 AZD9291 耐药 HCC827 的增殖,无论 c-Met 磷酸化水平如何。SHR-A1403 与过表达 c-Met 的耐药细胞结合后被内化到细胞中,并释放相关的微管抑制剂,导致细胞杀伤活性仅依赖于 c-Met 表达水平,而与 c-Met 或 EGFR 信号参与 AZD9291 耐药性无关。与体外活性一致,SHR-A1403 显著抑制 AZD9291 耐药 HCC827 肿瘤的生长,并在体内引起肿瘤消退。因此,我们的研究结果表明,SHR-A1403 能够有效地克服过表达 c-Met 的细胞中 AZD9291 的耐药性,进一步表明 c-Met 表达水平是预测 SHR-A1403 疗效的生物标志物。