Sharma Puja, Roberts Callie, Herpai Denise, Fokt Izabela D, Priebe Waldemar, Debinski Waldemar
Brain Tumor Center of Excellence, Wake Forest Baptist Medical Center Comprehensive Cancer Center, Winston-Salem, NC 27157, USA.
Department of Experimental Therapeutics, Division of Cancer Medicine, MD Anderson Cancer Center, Houston, TX 77054, USA.
Pharmaceuticals (Basel). 2020 Apr 23;13(4):77. doi: 10.3390/ph13040077.
Glioblastoma (GBM) is a complex and heterogeneous tumor that warrants a comprehensive therapeutic approach for treatment. Tumor-associated antigens offer an opportunity to selectively target various components of the GBM microenvironment while sparing the normal cells within the central nervous system. In this study, we conjugated a multivalent vector protein, QUAD 3.0, that can target four receptors: EphA3, EphA2, EphB2, and also IL-13RA2, spanning virtually 100% of the GBM microenvironment, to doxorubicin derivatives. The conjugates effectively bound to all four receptors, although to varying degrees, and delivered cytotoxic loads to both established and patient-derived GBM cell lines, with IC values in the low nM range. The conjugates were also non-toxic to animals. We anticipate that the QUAD 3.0 Dox conjugates will be further used in preclinical models and possibly clinics in the foreseeable future.
胶质母细胞瘤(GBM)是一种复杂的异质性肿瘤,需要采用综合治疗方法进行治疗。肿瘤相关抗原提供了一个机会,可以选择性地靶向GBM微环境的各个组成部分,同时避免对中枢神经系统内的正常细胞造成损伤。在本研究中,我们将一种多价载体蛋白QUAD 3.0与阿霉素衍生物偶联,该蛋白可靶向四种受体:EphA3、EphA2、EphB2以及IL-13RA2,几乎覆盖了100%的GBM微环境。这些偶联物能有效结合所有四种受体,尽管结合程度有所不同,并将细胞毒性负载传递给已建立的和患者来源的GBM细胞系,其IC值处于低纳摩尔范围。这些偶联物对动物也无毒。我们预计,在可预见的未来,QUAD 3.0阿霉素偶联物将进一步用于临床前模型,甚至可能用于临床。