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首页> 外文期刊>Japanese Journal of Cancer Research >Microarray Analysis of Gene-expression Profiles in Diffuse Large B-cell Lymphoma: Identification of Genes Related to Disease Progression.
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Microarray Analysis of Gene-expression Profiles in Diffuse Large B-cell Lymphoma: Identification of Genes Related to Disease Progression.

机译:弥漫性大B细胞淋巴瘤中基因表达谱的微阵列分析:疾病进展相关基因的鉴定。

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摘要

To identify genes that are associated with progression of malignant lymphoma, the expression profiles of 18 432 genes were analyzed in diffuse large B-cell lymphomas at early (stages I and II, 6 cases) and advanced stages (stages III and IV, 9 cases) by means of cDNA microarrays. By comparing expression profiles between localized and advanced lymphomas, a number of genes that were differentially expressed were identified: 48 genes with increased expression and 30 genes with reduced expression in advanced-stage diffuse large B-cell lymphomas. Increased expression of MPHOSPH1, RUVBL1, CHN2, PSA and CDC10 genes, and reduced expression of COL1A2, COL4A1, FBLN5, CLECSF6, MIC2, CAV1 and S100A10 genes in the advanced lymphoma group were confirmed by semi-quantitative reverse transcription-PCR. RUVBL1 and PSA expression was further confirmed by real-time quantitative PCR, whose results paralleled the microarray data. The highly expressed genes encode proteins that promote cell proliferation and the genes with reduced expression encode adhesion proteins and target protein for cytotoxic T-lymphocytes. These findings suggested that analysis with cDNA microarrays is a useful approach for identifying genes related to tumor progression and their products could be potential tumor markers or disease-specific targets for anti-tumor therapy.
机译:为了鉴定与恶性淋巴瘤进展相关的基因,分析了早期(I和II期,6例)和晚期(III和IV期,9例)的弥漫性大B细胞淋巴瘤中的18 432个基因的表达谱)通过cDNA芯片。通过比较局部淋巴瘤和晚期淋巴瘤的表达谱,鉴定了许多差异表达的基因:在晚期弥漫性大B细胞淋巴瘤中48个表达增加的基因和30个表达减少的基因。通过半定量逆转录-PCR证实了晚期淋巴瘤组中MPHOSPH1,RUVBL1,CHN2,PSA和CDC10基因的表达增加,而COL1A2,COL4A1,FBLN5,CLECSF6,MIC2,CAV1和S100A10基因的表达减少。通过实时定量PCR进一步证实了RUVBL1和PSA的表达,其结果与微阵列数据平行。高表达的基因编码促进细胞增殖的蛋白质,而表达降低的基因编码细胞毒性T淋巴细胞的粘附蛋白和靶标蛋白。这些发现表明,用cDNA微阵列分析是鉴定与肿瘤进展相关的基因的有用方法,其产物可能是潜在的肿瘤标志物或抗肿瘤治疗的疾病特异性靶标。

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