Laboratory for Cancer Molecular Biology, Department of Biological Sciences, Federal University of São Paulo, Diadema, Brazil.
Biostatistics Department, Pio XII Foundation, Barretos Cancer Hospital, Barretos, Brazil.
Mol Cancer Ther. 2015 Mar;14(3):828-34. doi: 10.1158/1535-7163.MCT-14-0796. Epub 2015 Jan 6.
Despite significant advances in the treatment of head and neck squamous cell carcinoma (HNSCC), the survival rate has not changed in the last decades. Therefore, the development of novel therapeutic strategies is pursued. Cancer-testis antigens (CTA) are strong immunogenic proteins with a tumor-restricted expression pattern, and are considered ideal targets for tumor-specific immunotherapeutic approaches. In this study, using an in silico approach, we selected, among 139 previously described CTA, candidates to be evaluated in 89 HNSCC and 20 normal mucosa samples. SPANX-CD (71.9%), MAGEB2 (44.9%), MAGEA1 (44.9%), MAGEB6 (32.6%), and CXORF48 (27.0%) were found frequently expressed in HNSCC, and over 85% of the tumors expressed at least one of these five CTAs. The mRNA positivity of CXORF48, MAGEB6, and CRISP2 presented significant associations with recognized clinical features for poor outcome. Furthermore, MAGEA3/6 positivity was associated with significantly better disease-free survival (DFS, P = 0.014), and the expression of this antigen was shown to be an independent prognostic factor for tumor recurrence. In conclusion, one of five selected CTAs is expressed in at least 85% of the HNSCCs, suggesting a possible usage as target for immunotherapeutic approaches, and the mRNA-positivity for MAGEA3/6 is shown to be an independent marker for DFS.
尽管头颈部鳞状细胞癌(HNSCC)的治疗取得了重大进展,但在过去几十年中,生存率并未改变。因此,正在寻求新的治疗策略。癌症睾丸抗原(CTA)是具有肿瘤特异性表达模式的强免疫原性蛋白,被认为是肿瘤特异性免疫治疗方法的理想靶标。在这项研究中,我们使用计算机方法,从之前描述的 139 个 CTA 中选择了候选者,以评估 89 例 HNSCC 和 20 例正常粘膜样本。SPANX-CD(71.9%),MAGEB2(44.9%),MAGEA1(44.9%),MAGEB6(32.6%)和 CXORF48(27.0%)在 HNSCC 中频繁表达,超过 85%的肿瘤表达这些 5 个 CTA 中的至少一个。 CXORF48、MAGEB6 和 CRISP2 的 mRNA 阳性与公认的预后不良的临床特征具有显著相关性。此外,MAGEA3/6 阳性与无病生存期(DFS)显著相关(P = 0.014),并且该抗原的表达被证明是肿瘤复发的独立预后因素。总之,五种选定的 CTA 中有一种在至少 85%的 HNSCC 中表达,表明可能用作免疫治疗方法的靶标,并且 MAGEA3/6 的 mRNA 阳性被证明是 DFS 的独立标志物。