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Cancer/Testis genes in multiple myeloma: expression patterns and prognosis value determined by microarray analysis. : Expression of cancer-testis genes in multiple myeloma

机译:多发性骨髓瘤中的癌症/睾丸基因:通过微阵列分析确定表达模式和预后价值。 :睾丸癌基因在多发性骨髓瘤中的表达

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摘要

Cancer-testis (CT) Ags are expressed in testis and malignant tumors but rarely in nongametogenic tissues. Due to this pattern, they represent attractive targets for cancer vaccination approaches. The aims of the present study are: 1) to assess the expression of CT genes on a pangenomic base in multiple myeloma (MM); 2) to assess the prognosis value of CT gene expression; and 3) to provide selection strategies for CT Ags in clinical vaccination trials. We report the expression pattern of CT genes in purified MM cells (MMC) of 64 patients with newly diagnosed MM and12 patients with monoclonal gammopathy of unknown significance, in normal plasma cell and B cell samples, and in 20 MMC lines. Of the 46 CT genes interrogated by the Affymetrix HG-U133 set arrays, 35 are expressed in the MMC of at least one patient. Of these, 25 are located on chromosome X. The expression of six CT genes is associated with a shorter event-free survival. The MMC of 98% of the patients express at least one CT gene, 86% at least two, and 70% at least three CT genes. By using a set of 10 CT genes including KM-HN-1, MAGE-C1, MAGE-A3/6/12, MAGE-A5, MORC, DDX43, SPACA3, SSX-4, GAGE-1-8, and MAGE-C2, a combination of at least three CT genes-desirable for circumventing tumor escape mechanisms-is obtained in the MMC of 67% of the patients. Provided that the immunogenicity of the products of these 10 CT genes is confirmed, gene expression profiling could be useful in identifying which CT Ags could be used to vaccinate a given patient.
机译:睾丸癌(CT)Ags在睾丸和恶性肿瘤中表达,但很少在非配子体组织中表达。由于这种模式,它们代表了癌症疫苗接种方法的诱人靶标。本研究的目的是:1)评估CT基因在多发性骨髓瘤(MM)的全基因组基础上的表达; 2)评估CT基因表达的预后价值;和3)在临床疫苗接种试验中提供CT Ag的选择策略。我们报告了CT基因在64名新诊断的MM患者和12名具有未知意义的单克隆性丙种病的患者的正常MM细胞(MMC)中,正常浆细胞和B细胞样本以及20个MMC细胞系中的表达模式。在Affymetrix HG-U133集阵列询问的46个CT基因中,有35个在至少一名患者的MMC中表达。其中25个位于X染色体上。六个C​​T基因的表达与较短的无事件生存期相关。 98%的患者的MMC表达至少一个CT基因,86%的至少两个CT基因和70%的至少三个CT基因。通过使用一组10个CT基因,包括KM-HN-1,MAGE-C1,​​MAGE-A3 / 6/12,MAGE-A5,MORC,DDX43,SPACA3,SSX-4,GAGE-1-8和MAGE-在MMC中,有67%的患者获得了C2,即至少三个CT基因的组合(可用于规避肿瘤逃逸机制)。如果已确认这10个CT基因产物的免疫原性,则基因表达谱分析可能有助于确定哪些CT Ag可以用于给特定患者接种疫苗。

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