He Shu-Jia, Gu Yong-Yao, Yu Liang, Luo Bin, Fan Rong, Lin Wen-Zhen, Lan Xiu-Wan, Lin Yong-Da, Zhang Qing-Mei, Xiao Shao-Wen, Xie Xiao-Xun
Department of Biochemistry and Molecular Biology, First Affiliated Hospital, Guangxi Medical University Nanning 530021, Guangxi Zhuang Autonomous Region, China.
Department of Pathology, First Affiliated Hospital, Guangxi Medical University Nanning 530021, Guangxi Zhuang Autonomous Region, China.
Int J Clin Exp Pathol. 2014 Apr 15;7(5):2350-60. eCollection 2014.
MAGE-D4 is a novel member of MAGE super-family. It has preliminarily been demonstrated that MAGE-D4 mRNA is not expressed in majority of normal tissues except for brain and ovary in which only trace amount of MAGE-D4 mRNA can be detected, but predominantly expressed in glioma. MAGE-D4 protein expression and its immunogenicity in glioma have not been elucidated well. This study was designed to analyze MAGE-D4 expression both at mRNA and protein level, characteristic of humoral immune response, and their relationships with glioma patients' clinicopathological parameters. Recombinant MAGE-D4 protein and antiserum were generated. Quantitative RT-PCR analysis revealed that MAGE-D4 mRNA expression was overall up-regulated in 41 glioma specimens compared with that in 14 normal brain tissues. Immunohistochemistry analysis showed that 78% (21/27) glioma tissues expressed MAGE-D4 protein, which was predominantly located in the cytoplasm of tumor cells, but absent in any neuroglia cell of normal brain tissues. ELISA analysis demonstrated that humoral response against MAGE-D4 was detected in 17% (7/41) of glioma patients' sera but not in 77 healthy donors. No apparent correlation was observed between the expression and immunogenicity of MAGE-D4 with clinicopathological parameters of glioma. In summary, these results indicate that MAGE-D4 is highly expressed in glioma and can develop specifically humoral response in glioma patients, which supports that it may be a promising biomarker for glioma diagnosis and immunotherapy.
MAGE-D4是MAGE超家族的一个新成员。初步研究表明,MAGE-D4 mRNA在大多数正常组织中不表达,仅在脑和卵巢中可检测到微量MAGE-D4 mRNA,而在胶质瘤中主要表达。MAGE-D4蛋白在胶质瘤中的表达及其免疫原性尚未得到充分阐明。本研究旨在分析MAGE-D4在mRNA和蛋白水平的表达、体液免疫反应特征及其与胶质瘤患者临床病理参数的关系。制备了重组MAGE-D4蛋白和抗血清。定量逆转录聚合酶链反应分析显示,与14例正常脑组织相比,41例胶质瘤标本中MAGE-D4 mRNA表达总体上调。免疫组织化学分析显示,78%(21/27)的胶质瘤组织表达MAGE-D4蛋白,主要位于肿瘤细胞的细胞质中,而在正常脑组织的任何神经胶质细胞中均未检测到。酶联免疫吸附测定分析表明,17%(7/41)的胶质瘤患者血清中检测到针对MAGE-D4的体液反应,而77名健康供体中未检测到。MAGE-D4的表达和免疫原性与胶质瘤的临床病理参数之间未观察到明显相关性。总之,这些结果表明,MAGE-D4在胶质瘤中高表达,并可在胶质瘤患者中引发特异性体液反应,这支持其可能是一种有前景的胶质瘤诊断和免疫治疗生物标志物。