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使用互补DNA微阵列对T细胞淋巴瘤细胞恶性进展过程中的基因表达谱进行比较基因组规模分析。

Comparative genome-scale analysis of gene expression profiles in T cell lymphoma cells during malignant progression using a complementary DNA microarray.

作者信息

Li S, Ross D T, Kadin M E, Brown P O, Wasik M A

机构信息

Department of Pathology and Laboratory Medicine, University of Pennsylvania Medical Center, Founders 7.06, 3400 Spruce Street, Philadelphia, PA 19104, USA.

出版信息

Am J Pathol. 2001 Apr;158(4):1231-7. doi: 10.1016/S0002-9440(10)64073-4.

Abstract

Using a cDNA microarray, we compared the expression of approximately 8000 genes between two unique, clonally related T cell lines derived from different stages of a progressive T cell lymphoma involving skin. A total of 180 genes was found to be differentially expressed at the RNA level by a factor of fivefold or greater. Compared with the cells from the earlier, clinically indolent stage of the lymphoma, 56 genes were up-regulated, whereas 124 genes were down-regulated in the cells from the advanced, clinically aggressive stage lymphoma. The functions of approximately 65% of these genes are currently unknown. The 22 genes with a known function that were up-regulated in the advanced lymphoma cells included several genes involved in promotion of cell proliferation and survival as well as drug resistance. The 42 functionally characterized genes that were down-regulated in the advanced lymphoma cells included negative regulators of cell activation and cell cycle, and mediators of cell adhesion, apoptosis, and genome integrity. The differential expression identified by the cDNA microarray analysis was confirmed for selected genes by reverse transcription-polymerase chain reaction and Northern blotting. The identified differences in gene expression may be related to the differences in behavior between the early and advanced stages of the T cell lymphoma and point to directions for further investigations into mechanisms of lymphoma progression.

摘要

我们使用cDNA微阵列,比较了源自累及皮肤的进行性T细胞淋巴瘤不同阶段的两个独特的、克隆相关的T细胞系之间约8000个基因的表达情况。共发现180个基因在RNA水平上有五倍或更高倍数的差异表达。与淋巴瘤早期临床惰性阶段的细胞相比,晚期临床侵袭性阶段淋巴瘤细胞中有56个基因上调,124个基因下调。这些基因中约65%的功能目前尚不清楚。在晚期淋巴瘤细胞中上调的22个具有已知功能的基因包括几个参与促进细胞增殖、存活以及耐药性的基因。在晚期淋巴瘤细胞中下调的42个功能已明确的基因包括细胞活化和细胞周期的负调节因子,以及细胞黏附、凋亡和基因组完整性的介质。通过逆转录-聚合酶链反应和Northern印迹法对cDNA微阵列分析鉴定出的差异表达的选定基因进行了验证。所确定的基因表达差异可能与T细胞淋巴瘤早期和晚期行为的差异有关,并为进一步研究淋巴瘤进展机制指明了方向。

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