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用于靶向胶质母细胞瘤中Eph受体的药物偶联物

Drug Conjugates for Targeting Eph Receptors in Glioblastoma.

作者信息

Sharma Puja, Roberts Callie, Herpai Denise, Fokt Izabela D, Priebe Waldemar, Debinski Waldemar

机构信息

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.

出版信息

Pharmaceuticals (Basel). 2020 Apr 23;13(4):77. doi: 10.3390/ph13040077.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43e4/7243104/2c5501993345/pharmaceuticals-13-00077-g002.jpg

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