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热诱导人淋巴瘤 U937 细胞凋亡相关的基因网络。

Gene networks involved in apoptosis induced by hyperthermia in human lymphoma U937 cells.

机构信息

Department of Radiological Sciences, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama 930-0194, Japan.

出版信息

Cell Biol Int. 2009 Dec;33(12):1253-62. doi: 10.1016/j.cellbi.2009.08.009. Epub 2009 Sep 2.

Abstract

To define the molecular mechanisms that mediate hyperthermia-induced apoptosis, we performed microarray and computational gene expression analyses. U937 cells, a human myelomonocytic lymphoma cell line, were treated with hyperthermia at 42 degrees C for 90 min and cultured at 37 degrees C. Apoptotic cells ( approximately 15%) were seen 6 h after hyperthermic treatment, and elevated expression of heat shock proteins (HSPs) including Hsp27, Hsp40, and Hsp70 was detected, following the activation of heat shock factor-1. Of the 54,675 probe sets analyzed, 1334 were upregulated and 4214 were downregulated by >2.0-fold in the cells treated with hyperthermia. A non-hierarchical gene clustering algorithm, K-means clustering, demonstrated 10 gene clusters. The gene network U1 or U2 that was obtained from up-regulated genes in cluster I or IX contained HSPA1B, DNAJB1, HSPH1, and TXN or PML, LYN, and DUSP1, and were mainly associated with cellular compromise, and cellular function and maintenance or death, and cancer, respectively. In the decreased gene cluster II, the gene network D1 including CCNE1 and CEBPE was associated with the cell cycle and cellular growth and proliferation. These findings will provide a basis for understanding the detailed molecular mechanisms of apoptosis induced by hyperthermia at 42 degrees C in cells.

摘要

为了定义介导高热诱导细胞凋亡的分子机制,我们进行了基因表达谱分析和计算分析。将人髓单核白血病细胞系 U937 细胞在 42℃下加热 90 分钟,然后在 37℃下培养。热疗后 6 小时可观察到凋亡细胞(约 15%),并检测到热休克蛋白(HSPs)包括 Hsp27、Hsp40 和 Hsp70 的表达上调,这是热休克因子-1 激活的结果。在分析的 54675 个探针集中,有 1334 个被上调,4214 个被上调超过 2.0 倍在热疗处理的细胞中。非层次聚类算法 K-means 聚类显示出 10 个基因簇。从簇 I 或 IX 的上调基因中获得的基因网络 U1 或 U2 包含 HSPA1B、DNAJB1、HSPH1 和 TXN 或 PML、LYN 和 DUSP1,主要与细胞损伤、细胞功能和维持或死亡以及癌症有关。在下调基因簇 II 中,基因网络 D1 包括 CCNE1 和 CEBPE,与细胞周期以及细胞生长和增殖有关。这些发现将为理解 42℃高温诱导细胞凋亡的详细分子机制提供基础。

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