Laboratory of Oncology, Translational Research and Laboratory Medicine, G. Gaslini Institute Genoa, Italy.
Front Oncol. 2012 Nov 16;2:174. doi: 10.3389/fonc.2012.00174. eCollection 2012.
MYCN is a well-known oncogene over-expressed in different human malignancies including neuroblastoma (NB), rhabdomyosarcoma, medulloblastoma, astrocytoma, Wilms' tumor, and small cell lung cancer. In the case of NB, MYCN amplification is an established biomarker of poor-prognosis. MYCN belongs to a family of transcription factors (the most important of which is C-MYC) that show a high degree of homology. Down-regulation of MYC protein expression leads to tumor regression in animal models, indicating that MYC proteins represent interesting therapeutic targets. Pre-requisites for a candidate tumor-associated antigen (TAA) to be targeted by immunotherapeutic approaches are the following, (i) expression should be tumor-restricted, (ii) the putative TAA should be up-regulated in cancer cells, and (iii) protein should be processed into immunogenic peptides capable of associating to major histocompatibility complex molecules with high affinity. Indeed, the MYCN protein is not expressed in human adult tissues and up-regulated variably in NB cells, and MYCN peptides capable of associating to HLA-A1 or HLA-A2 molecules with high affinity have been identified. Thus the MYCN protein qualifies as putative TAA in NB. Additional issues that determine the feasibility of targeting a putative TAA with cytotoxic T lymphocytes (CTLs) and will be here discussed are the following, (i) the inadequacy of tumor cells per se to act as antigen-presenting cells witnessed, in the case of NB cells, by the low to absent expression of HLA class I molecules, the lack of co-stimulatory molecules and multiple defects in the HLA class I related antigen processing machinery, and (ii) the immune evasion mechanisms operated by cancer cells to fool the host immune system, such as up-regulation of soluble immunosuppressive molecules (e.g., soluble MICA and HLA-G in the case of NB) or generation of immunosuppressive cells in the tumor microenvironment. A final issue that deserves consideration is the strategy used to generate CTL.
MYCN 是一种在多种人类恶性肿瘤中过度表达的已知癌基因,包括神经母细胞瘤 (NB)、横纹肌肉瘤、髓母细胞瘤、星形细胞瘤、肾母细胞瘤和小细胞肺癌。在 NB 的情况下,MYCN 扩增是预后不良的既定生物标志物。MYCN 属于转录因子家族(最重要的是 C-MYC),它们具有高度同源性。下调 MYC 蛋白表达会导致动物模型中的肿瘤消退,表明 MYC 蛋白代表了有趣的治疗靶点。候选肿瘤相关抗原 (TAA) 被免疫治疗方法靶向的前提条件如下,(i) 表达应仅限于肿瘤,(ii) 假定的 TAA 应在癌细胞中上调,并且 (iii) 蛋白质应被加工成能够与主要组织相容性复合物分子以高亲和力结合的免疫原性肽。事实上,MYCN 蛋白在人类成人组织中不表达,并且在 NB 细胞中不同程度地上调,并且已经鉴定出能够与 HLA-A1 或 HLA-A2 分子以高亲和力结合的 MYCN 肽。因此,MYCN 蛋白在 NB 中被视为潜在的 TAA。决定用细胞毒性 T 淋巴细胞 (CTL) 靶向潜在 TAA 的可行性的其他问题将在这里讨论,(i) 肿瘤细胞本身充当抗原呈递细胞的不足,在 NB 细胞的情况下,表现为 HLA 类 I 分子的低表达或不存在、缺乏共刺激分子和 HLA 类 I 相关抗原加工机制的多个缺陷,以及 (ii) 癌细胞逃避宿主免疫系统的免疫逃逸机制,例如上调可溶性免疫抑制分子(例如,在 NB 的情况下,可溶性 MICA 和 HLA-G)或在肿瘤微环境中产生免疫抑制细胞。最后一个值得考虑的问题是用于生成 CTL 的策略。