Suzuki Maya, Cheung Nai-Kong V
Memorial Sloan Kettering Cancer Center, Department of Pediatrics , 1275 York Avenue, New York, NY 10065 , USA +1 646 888 2313 ; +1 631 422 0452 ;
Expert Opin Ther Targets. 2015 Mar;19(3):349-62. doi: 10.1517/14728222.2014.986459. Epub 2015 Jan 20.
Ganglioside GD2 is found in vertebrates and invertebrates, overexpressed among pediatric and adult solid tumors, including neuroblastoma, glioma, retinoblastoma, Ewing's family of tumors, rhabdomyosarcoma, osteosarcoma, leiomyosarcoma, liposarcoma, fibrosarcoma, small cell lung cancer and melanoma. It is also found on stem cells, neurons, some nerve fibers and basal layer of the skin.
GD2 provides a promising clinical target for radiolabeled antibodies, bispecific antibodies, chimeric antigen receptor (CAR)-modified T cells, drug conjugates, nanoparticles and vaccines. Here, we review its biochemistry, normal physiology, role in tumorigenesis, important characteristics as a target, as well as anti-GD2-targeted strategies.
Bridging the knowledge gaps in understanding the interactions of GD2 with signaling molecules within the glycosynapses, and the regulation of its cellular expression should improve therapeutic strategies targeting this ganglioside. In addition to anti-GD2 IgG mAbs, their drug conjugates, radiolabeled forms especially when genetically engineered to improve therapeutic index and novel bispecific forms or CARs to retarget T-cells are promising candidates for treating metastatic cancers.
神经节苷脂GD2存在于脊椎动物和无脊椎动物中,在小儿和成人实体瘤中过表达,包括神经母细胞瘤、神经胶质瘤、视网膜母细胞瘤、尤因氏肿瘤家族、横纹肌肉瘤、骨肉瘤、平滑肌肉瘤、脂肪肉瘤、纤维肉瘤、小细胞肺癌和黑色素瘤。它也存在于干细胞、神经元、一些神经纤维和皮肤基底层上。
GD2为放射性标记抗体、双特异性抗体、嵌合抗原受体(CAR)修饰的T细胞、药物偶联物、纳米颗粒和疫苗提供了一个有前景的临床靶点。在此,我们综述其生物化学、正常生理学、在肿瘤发生中的作用、作为靶点的重要特征以及抗GD2靶向策略。
弥合在理解GD2与糖突触内信号分子相互作用以及其细胞表达调控方面的知识差距,应能改进针对这种神经节苷脂的治疗策略。除了抗GD2 IgG单克隆抗体、它们的药物偶联物、放射性标记形式(特别是经过基因工程改造以提高治疗指数时)以及用于重新靶向T细胞的新型双特异性形式或CARs外,它们都是治疗转移性癌症的有前景的候选药物。