Mamot Christoph, Drummond Daryl C, Greiser Udo, Hong Keelung, Kirpotin Dmitri B, Marks James D, Park John W
Division of Hematology-Oncology, University of California, San Francisco, 94115, USA.
Cancer Res. 2003 Jun 15;63(12):3154-61.
We hypothesized that immunoliposomes (ILs) that target epidermal growth factor receptor (EGFR) and/or its truncated variant EGFRvIII can be constructed to provide efficient intracellular drug delivery in tumor cells overexpressing these receptors. Monoclonal antibody fragments included Fab' fragments derived from C225, which binds both EGFR and EGFRvIII, or novel anti-EGFR scFv C10, which binds EGFR only. Monoclonal antibody fragments were covalently linked to liposomes containing various reporters or drugs. ILs were evaluated for specific binding, internalization, and cytotoxicity in EGFR/EGFRvIII-overexpressing cell lines in vitro. Flow cytometry and fluorescence microscopy showed that EGFR-targeted ILs, but not nontargeted liposomes or irrelevant ILs, were efficiently bound and internalized by EGFR-overexpressing cells, including glioma cells (U-87), carcinoma cells (A-431 and MDA-MB-468), and EGFRvIII stable transfectants (NR-6M). Furthermore, EGFR-targeted ILs did not bind to non-EGFR-overexpressing cells (MCF-7 and parental NR-6). ILs showed 3 orders of magnitude greater accumulation in NR-6-EGFRvIII stable transfectants versus parental NR-6 cells. Quantitative internalization studies indicated binding of EGFR-targeted ILs to target cells within 5 min, followed by intracellular accumulation beginning at 15 min; total uptake reached approximately 13,000 ILs/cell. ILs were used to deliver cytotoxic drugs doxorubicin, vinorelbine, or methotrexate to EGFR/EGFRvIII-overexpressing target cells in vitro. In each case, the IL agent was significantly more cytotoxic than the corresponding nontargeted liposomal drug in target cells, whereas it was equivalent in cells lacking EGFR/EGFRvIII overexpression. We conclude that EGFR-targeted ILs provide efficient and targeted delivery of anticancer drugs in cells overexpressing EGFR or EGFRvIII.
我们推测,可以构建靶向表皮生长因子受体(EGFR)和/或其截短变体EGFRvIII的免疫脂质体(ILs),以便在过表达这些受体的肿瘤细胞中实现高效的细胞内药物递送。单克隆抗体片段包括源自C225的Fab'片段,其可同时结合EGFR和EGFRvIII,或新型抗EGFR单链抗体片段(scFv)C10,其仅结合EGFR。单克隆抗体片段与含有各种报告分子或药物的脂质体共价连接。在体外对EGFR/EGFRvIII过表达的细胞系中,评估了ILs的特异性结合、内化和细胞毒性。流式细胞术和荧光显微镜检查显示,靶向EGFR的ILs而非非靶向脂质体或无关的ILs,能够被过表达EGFR的细胞有效结合和内化,这些细胞包括胶质瘤细胞(U-87)、癌细胞(A-431和MDA-MB-468)以及EGFRvIII稳定转染细胞(NR-6M)。此外,靶向EGFR的ILs不与未过表达EGFR的细胞(MCF-7和亲本NR-6)结合。与亲本NR-6细胞相比,ILs在NR-6-EGFRvIII稳定转染细胞中的积累高出3个数量级。定量内化研究表明,靶向EGFR的ILs在5分钟内与靶细胞结合,随后在15分钟开始细胞内积累;总摄取量达到约13,000个ILs/细胞。在体外,ILs被用于将细胞毒性药物阿霉素、长春瑞滨或甲氨蝶呤递送至过表达EGFR/EGFRvIII的靶细胞。在每种情况下,IL制剂在靶细胞中的细胞毒性均显著高于相应的非靶向脂质体药物,而在缺乏EGFR/EGFRvIII过表达的细胞中,二者相当。我们得出结论,靶向EGFR的ILs能够在过表达EGFR或EGFRvIII的细胞中实现高效且靶向的抗癌药物递送。