Dobrenkov Konstantin, Ostrovnaya Irina, Gu Jessie, Cheung Irene Y, Cheung Nai-Kong V
Department of Pediatrics, Memorial Sloan Kettering Cancer Center, New York.
Department of Biostatistics and Epidemiology, Memorial Sloan Kettering Cancer Center, New York.
Pediatr Blood Cancer. 2016 Oct;63(10):1780-5. doi: 10.1002/pbc.26097. Epub 2016 Jun 15.
GD2 and GD3 are the tumor-associated glycolipid antigens found in a broad spectrum of human cancers. GD2-specific antibody is currently a standard of care for high-risk neuroblastoma therapy. In this study, the pattern of GD2 and GD3 expression among pediatric/adolescent or young adult tumors was determined, providing companion diagnostics for targeted therapy.
Ninety-two specimens of human osteosarcoma (OS), rhabdomyosarcoma (RMS), Ewing family of tumors, desmoplastic small round cell tumor (DSRCT), and melanoma were analyzed for GD2/GD3 expression by immunohistochemistry. Murine monoclonal antibody 3F8 was used for GD2 staining, and R24 for GD3. Staining was scored according to both intensity and percentage of positive tumor cells from 0 to 4.
Both gangliosides were highly prevalent in OS and melanoma. Among other tumors, GD3 expression was higher than GD2 expression. Most OS samples demonstrated strong staining for GD2 and GD3, whereas expression for other tumors was highly variable. Mean intensity of GD2 expression was significantly more heterogeneous (P < 0.001) when compared to GD3 across tumor types. When assessing the difference between GD2 and GD3 expression in all tumor types combined, GD3 expression had a significantly higher score (P = 0.049). When analyzed within each cancer, GD3 expression was significantly higher only in DSRCT (P = 0.002). There was no statistical difference in either GD2 or GD3 expression between primary and recurrent sarcomas.
GD2/GD3 expression among pediatric solid tumors is common, albeit with variable level of expression. Especially for patients with sarcoma, these gangliosides can be potential targets for antibody-based therapies.
GD2和GD3是在多种人类癌症中发现的肿瘤相关糖脂抗原。GD2特异性抗体目前是高危神经母细胞瘤治疗的标准治疗方法。在本研究中,确定了儿科/青少年或年轻成人肿瘤中GD2和GD3的表达模式,为靶向治疗提供伴随诊断。
通过免疫组织化学分析了92例人类骨肉瘤(OS)、横纹肌肉瘤(RMS)、尤因家族肿瘤、促结缔组织增生性小圆细胞肿瘤(DSRCT)和黑色素瘤标本中的GD2/GD3表达。鼠单克隆抗体3F8用于GD2染色,R24用于GD3染色。根据阳性肿瘤细胞的强度和百分比从0到4对染色进行评分。
两种神经节苷脂在骨肉瘤和黑色素瘤中高度普遍。在其他肿瘤中,GD3表达高于GD2表达。大多数骨肉瘤样本显示GD2和GD3染色强,而其他肿瘤的表达高度可变。与GD3相比,GD2表达的平均强度在不同肿瘤类型中差异显著更大(P < 0.001)。在所有肿瘤类型中评估GD2和GD3表达的差异时,GD3表达得分显著更高(P = 0.049)。在每种癌症中分析时,GD3表达仅在促结缔组织增生性小圆细胞肿瘤中显著更高(P = 0.002)。原发性和复发性肉瘤之间GD2或GD3表达均无统计学差异。
儿科实体瘤中GD2/GD3表达常见,尽管表达水平不同。特别是对于肉瘤患者,这些神经节苷脂可能是基于抗体治疗的潜在靶点。