Laboratorio de Mecanismos Moleculares de Carcinogénesis, Instituto de Biología y Medicina Experimental (IBYME-CONICET), Buenos Aires, Argentina.
Department of Medicine, Weill Cornell Medical College, New York, New York.
Clin Cancer Res. 2017 Feb 1;23(3):636-648. doi: 10.1158/1078-0432.CCR-16-0970. Epub 2016 Oct 3.
Although trastuzumab administration improved the outcome of HER2-positive breast cancer patients, resistance events hamper its clinical benefits. We demonstrated that TNFα stimulation in vitro induces trastuzumab resistance in HER2-positive breast cancer cell lines. Here, we explored the mechanism of TNFα-induced trastuzumab resistance and the therapeutic strategies to overcome it.
Trastuzumab-sensitive breast cancer cells, genetically engineered to stably overexpress TNFα, and de novo trastuzumab-resistant tumors, were used to evaluate trastuzumab response and TNFα-blocking antibodies effectiveness respectively. Immunohistochemistry and antibody-dependent cell cytotoxicity (ADCC), together with siRNA strategy, were used to explore TNFα influence on the expression and function of its downstream target, mucin 4 (MUC4). The clinical relevance of MUC4 expression was studied in a cohort of 78 HER2-positive breast cancer patients treated with adjuvant trastuzumab.
TNFα overexpression turned trastuzumab-sensitive cells and tumors into resistant ones. Histopathologic findings revealed mucin foci in TNFα-producing tumors. TNFα induced upregulation of MUC4 that reduced trastuzumab binding to its epitope and impaired ADCC. Silencing MUC4 enhanced trastuzumab binding, increased ADCC, and overcame trastuzumab and trastuzumab-emtansine antiproliferative effects in TNFα-overexpressing cells. Accordingly, administration of TNFα-blocking antibodies downregulated MUC4 and sensitized de novo trastuzumab-resistant breast cancer cells and tumors to trastuzumab. In HER2-positive breast cancer samples, MUC4 expression was found to be an independent predictor of poor disease-free survival (P = 0.008).
We identified TNFα-induced MUC4 expression as a novel trastuzumab resistance mechanism. We propose MUC4 expression as a predictive biomarker of trastuzumab efficacy and a guide to combination therapy of TNFα-blocking antibodies with trastuzumab. Clin Cancer Res; 23(3); 636-48. ©2016 AACR.
曲妥珠单抗的应用改善了 HER2 阳性乳腺癌患者的预后,但耐药事件会影响其临床获益。我们体外研究显示 TNFα 刺激可诱导 HER2 阳性乳腺癌细胞系对曲妥珠单抗产生耐药性。在此,我们探索了 TNFα 诱导曲妥珠单抗耐药的机制及克服该耐药的治疗策略。
我们分别使用曲妥珠单抗敏感的乳腺癌细胞系和经基因工程稳定过表达 TNFα 的细胞系、以及新出现的曲妥珠单抗耐药肿瘤,来评估曲妥珠单抗的反应和 TNFα 阻断抗体的疗效。我们采用免疫组化和抗体依赖性细胞毒性(ADCC)检测,以及 siRNA 策略,来探讨 TNFα 对其下游靶标粘蛋白 4(MUC4)表达和功能的影响。我们对 78 例接受辅助曲妥珠单抗治疗的 HER2 阳性乳腺癌患者的队列进行了 MUC4 表达的临床相关性研究。
TNFα 过表达使曲妥珠单抗敏感的细胞系和肿瘤变为耐药。组织病理学发现 TNFα 产生的肿瘤中有粘蛋白灶。TNFα 诱导 MUC4 上调,从而减少了曲妥珠单抗与表位的结合,并损害了 ADCC。沉默 MUC4 增强了曲妥珠单抗的结合,增加了 ADCC,并克服了 TNFα 过表达细胞中曲妥珠单抗和曲妥珠单抗-美坦新的抗增殖作用。相应地,TNFα 阻断抗体的给药下调了 MUC4,并使新出现的曲妥珠单抗耐药的乳腺癌细胞系和肿瘤对曲妥珠单抗敏感。在 HER2 阳性乳腺癌样本中,MUC4 的表达被确定为无病生存不良的独立预测因子(P = 0.008)。
我们确定了 TNFα 诱导的 MUC4 表达是曲妥珠单抗耐药的新机制。我们提出 MUC4 表达是曲妥珠单抗疗效的预测生物标志物,并建议将 MUC4 表达作为 TNFα 阻断抗体与曲妥珠单抗联合治疗的指导。
临床癌症研究;23(3);636-48. ©2016AACR.