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利用cDNA微阵列技术对云芝PSP诱导人早幼粒细胞白血病HL-60细胞凋亡进行分子特征分析。

Molecular characterization of Coriolus versicolor PSP-induced apoptosis in human promyelotic leukemic HL-60 cells using cDNA microarray.

作者信息

Zeng Fanya, Hon Chung-Chau, Sit Wai-Hung, Chow Ken Yan-Ching, Hui Raymond Kin-Hi, Law Ivy Ka-Man, Ng Victor Wai-Lap, Yang Xiao-Tong, Leung Frederick Chi-Ching, Wan Jennifer Man-Fan

机构信息

Department of Zoology, The University of Hong Kong, Hong Kong, SAR, P.R. China.

出版信息

Int J Oncol. 2005 Aug;27(2):513-23.

Abstract

Proteins and peptide bound polysaccharides (PSP) extracted from Basidiomycetous fungi are widely used in cancer immunotherapy and recently demonstrated to induce apoptosis in cancer cells in vitro. In order to provide the molecular pharmacological mechanisms of PSP on human cancer cells, we investigated the gene expression profiles of PSP-treated apoptotic human promyelotic leukemic HL-60 cells using ResGen 40k IMAGE printed cDNA microarray. In total 378 and 111 transcripts were identified as differentially expressed in the apoptotic cells by at least a factor of 2 or 3, respectively. Our data show that PSP-induced apoptosis in HL-60 cells might be mediated by up-regulation of early transcription factors such as AP-1, EGR1, IER2 and IER5, and down-regulation of NF-kappaB transcription pathways. Other gene expression changes, including the increase of several apoptotic or anti-proliferation genes, such as GADD45A/B and TUSC2, and the decrease of a batch of phosphatase and kinase genes, may also provide further evidences in supporting the process of PSP induced apoptosis in cancer cells. Some of the well-characterized carcinogenesis-related gene transcripts such as SAT, DCT, Melan-A, uPA and cyclin E1 were also alternated by PSP in the HL-60 cells. These transcripts can be employed as markers for quality control of PSP products on functional levels. The present study provides new insight into the molecular mechanisms involved in PSP-induced apoptosis in leukemic HL-60 cells analyzed by cDNA microarray.

摘要

从担子菌纲真菌中提取的蛋白质和肽结合多糖(PSP)被广泛应用于癌症免疫治疗,最近的研究表明其在体外可诱导癌细胞凋亡。为了揭示PSP对人癌细胞作用的分子药理机制,我们使用ResGen 40k IMAGE打印cDNA微阵列研究了经PSP处理后发生凋亡的人早幼粒细胞白血病HL-60细胞的基因表达谱。总共分别鉴定出378个和111个转录本在凋亡细胞中差异表达,差异倍数至少为2倍或3倍。我们的数据表明,PSP诱导HL-60细胞凋亡可能是通过上调早期转录因子如AP-1、EGR1、IER2和IER5以及下调NF-κB转录途径来介导的。其他基因表达变化,包括一些凋亡或抗增殖基因如GADD45A/B和TUSC2的增加,以及一批磷酸酶和激酶基因的减少,也可能为支持PSP诱导癌细胞凋亡的过程提供进一步证据。一些已明确的与致癌作用相关的基因转录本如SAT、DCT、Melan-A、uPA和细胞周期蛋白E1在HL-60细胞中也被PSP改变。这些转录本可作为PSP产品功能水平质量控制的标志物。本研究通过cDNA微阵列分析为PSP诱导白血病HL-60细胞凋亡所涉及的分子机制提供了新的见解。

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