首页> 美国卫生研究院文献>Neoplasia (New York N.Y.) >In Pancreatic Carcinoma Dual EGFR/HER2 Targeting with Cetuximab/Trastuzumab Is More Effective than Treatment with Trastuzumab/Erlotinib or Lapatinib Alone: Implication of Receptors Down-regulation and Dimers Disruption
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In Pancreatic Carcinoma Dual EGFR/HER2 Targeting with Cetuximab/Trastuzumab Is More Effective than Treatment with Trastuzumab/Erlotinib or Lapatinib Alone: Implication of Receptors Down-regulation and Dimers Disruption

机译:在胰腺癌中西妥昔单抗/曲妥珠单抗双重靶向EGFR / HER2比单用曲妥珠单抗/厄洛替尼或拉帕替尼治疗更有效:受体下调和二聚体破坏的含义

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摘要

We previously demonstrated the synergistic therapeutic effect of the cetuximab (anti-epidermal growth factor receptor [EGFR] monoclonal antibody, mAb)-trastuzumab (anti-HER2 mAb) combination (2mAbs therapy) in HER2low human pancreatic carcinoma xenografts. Here, we compared the 2mAbs therapy, the erlotinib (EGFR tyrosine kinase inhibitor [TKI])-trastuzumab combination and lapatinib alone (dual HER2/EGFR TKI) and explored their possible mechanisms of action. The effects on tumor growth and animal survival of the three therapies were assessed in nude mice xenografted with the human pancreatic carcinoma cell lines Capan-1 and BxPC-3. After therapy, EGFR and HER2 expression and AKT phosphorylation in tumor cells were analyzed by Western blot analysis. EGFR/HER2 heterodimerization was quantified in BxPC-3 cells by time-resolved FRET. In K-ras-mutated Capan-1 xenografts, the 2mAbs therapy gave significantly higher inhibition of tumor growth than the erlotinib/trastuzumab combination, whereas in BxPC-3 (wild-type K-ras) xenografts, the erlotinib/trastuzumab combination showed similar growth inhibition but fewer tumor-free mice. Lapatinib showed no antitumor effect in both types of xenografts. The efficacy of the 2mAbs therapy was partly Fc-independent because F(ab′)2 fragments of the two mAbs significantly inhibited BxPC-3 growth, although with a time-limited therapeutic effect. The 2mAbs therapy was associated with a reduction of EGFR and HER2 expression and AKT phosphorylation. BxPC-3 cells preincubated with the two mAbs showed 50% less EGFR/HER2 heterodimers than controls. In pancreatic carcinoma xenografts, the 2mAbs therapy is more effective than treatments involving dual EGFR/HER2 TKIs. The mechanism of action may involve decreased AKT phosphorylation and/or disruption of EGFR/HER2 heterodimerization.
机译:先前我们证明了西妥昔单抗(抗表皮生长因子受体[EGFR]单克隆抗体,mAb)-曲妥珠单抗(抗HER2 mAb)组合(2mAbs治疗)在HER2 人胰腺中的协同治疗作用异种移植癌。在这里,我们比较了2mAbs疗法,厄洛替尼(EGFR酪氨酸激酶抑制剂[TKI])-曲妥珠单抗和单独拉帕替尼(双重HER2 / EGFR TKI)的组合,并探讨了其可能的作用机制。在异种移植了人类胰腺癌细胞系Capan-1和BxPC-3的裸鼠中评估了这三种疗法对肿瘤生长和动物存活的影响。治疗后,通过蛋白质印迹分析来分析肿瘤细胞中的EGFR和HER2表达以及AKT磷酸化。通过时间分辨FRET对BxPC-3细胞中的EGFR / HER2异源二聚化进行了定量。在K-ras突变的Capan-1异种移植物中,与erlotinib / trastuzumab组合相比,2mAbs治疗对肿瘤生长的抑制作用明显更高,而在BxPC-3(野生型K-ras)异种移植中,erlotinib / trastuzumab组合显示出相似的抑制作用。生长抑制,但无肿瘤小鼠减少。拉帕替尼在两种异种移植物中均未显示出抗肿瘤作用。 2mAbs治疗的疗效部分不依赖于Fc,因为两个mAb的F(ab')2片段显着抑制BxPC-3的生长,尽管具有限时的治疗效果。 2mAbs治疗与EGFR和HER2表达减少以及AKT磷酸化有关。与两种mAb预孵育的BxPC-3细胞显示的EGFR / HER2异二聚体比对照少50%。在胰腺癌异种移植物中,2mAbs治疗比涉及双重EGFR / HER2 TKI的治疗更有效。作用机制可能涉及减少AKT磷酸化和/或破坏EGFR / HER2异二聚体。

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