Huang S M, Harari P M
Department of Human Oncology, University of Wisconsin School of Medicine and Comprehensive Cancer Center, Madison 53792-0600, USA.
Clin Cancer Res. 2000 Jun;6(6):2166-74.
We have recently demonstrated that molecular blockade of the epidermal growth factor receptor with the anti-epidermal growth factor receptor (EGFR) monoclonal antibody C225 enhances the in vitro radiosensitivity of human squamous cell carcinomas (SCCs) derived from the head and neck. In the present study, we further investigated the capacity of C225 to modulate the in vitro and in vivo radiation response of human SCC tumor cells and xenografts, and we examined several potential mechanisms that may contribute to the enhanced radiation response induced by C225. Tumor xenograft studies demonstrated complete regression of both newly established (20 mm3) and well-established (100 mm3) SCC tumors over a 55-100 day follow-up period in athymic mice treated with the combination of C225 (i.p. injection) and radiation. Cell cycle analysis via flow cytometry confirmed that combined treatment with C225 and radiation induced an accumulation of cells in the more radiosensitive cell cycle phases (G1, G2-M) with concurrent reduction in the proportion of cells in the more radioresistant S phase. Results from sublethal damage repair and potentially lethal damage repair analyses in cultured SCC cells demonstrated a strong inhibitory effect of C225 on postradiation damage repair. Further, exposure of SCC cells to C225 induced a redistribution of DNA-dependent protein kinase from the nucleus to the cytosol, suggesting one potential mechanism whereby C225 may influence the cellular response to radiation. Immunohistochemical analysis of SCC tumor xenografts after systemic administration of C225 demonstrated inhibition of the in vivo expression of tumor angiogenesis markers, including vascular endothelial growth factor and Factor VIII. Taken together, the collective data suggest that the profound in vivo antitumor activity identified in the xenograft setting when C225 is combined with radiation derives from more than simply the antiproliferative and cell cycle effects of EGFR system inhibition. In addition to antiproliferative growth inhibition, EGFR blockade with C225 appears to influence the capacity of human SCCs to effect DNA repair after exposure to radiation, and to express classic markers of tumor angiogenesis.
我们最近已证明,用抗表皮生长因子受体(EGFR)单克隆抗体C225对表皮生长因子受体进行分子阻断可增强源自头颈部的人鳞状细胞癌(SCC)的体外放射敏感性。在本研究中,我们进一步研究了C225调节人SCC肿瘤细胞和异种移植物的体外及体内辐射反应的能力,并研究了几种可能导致C225诱导的辐射反应增强的潜在机制。肿瘤异种移植研究表明,在用C225(腹腔注射)和辐射联合治疗的无胸腺小鼠中,新建立的(20 mm3)和已形成的(100 mm3)SCC肿瘤在55 - 100天的随访期内完全消退。通过流式细胞术进行的细胞周期分析证实,C225与辐射联合治疗诱导细胞在更具放射敏感性的细胞周期阶段(G1期、G2 - M期)积累,同时降低了更具放射抗性的S期细胞比例。对培养的SCC细胞进行的亚致死损伤修复和潜在致死损伤修复分析结果表明,C225对辐射后损伤修复具有强烈的抑制作用。此外,将SCC细胞暴露于C225会导致DNA依赖性蛋白激酶从细胞核重新分布到细胞质中,这表明C225可能影响细胞对辐射反应的一种潜在机制。在全身给予C225后,对SCC肿瘤异种移植物进行免疫组织化学分析表明,肿瘤血管生成标志物(包括血管内皮生长因子和因子VIII)的体内表达受到抑制。综上所述,这些总体数据表明,当C225与辐射联合使用时,在异种移植模型中所确定的显著体内抗肿瘤活性不仅仅源于EGFR系统抑制的抗增殖和细胞周期效应。除了抗增殖生长抑制外,用C225阻断EGFR似乎还会影响人SCC在受到辐射后进行DNA修复的能力以及表达肿瘤血管生成经典标志物的能力。