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多沙唑嗪通过DNA结合和DNA依赖性蛋白激酶下调诱导LNCaP前列腺癌细胞系凋亡。

Doxazosin induces apoptosis in LNCaP prostate cancer cell line through DNA binding and DNA-dependent protein kinase down-regulation.

作者信息

Arencibia José M, Del Rio Mónica, Bonnin Ana, Lopes Rita, Lemoine Nicholas R, López-Barahona Mónica

机构信息

Departamento de Bioquímica, Facultad de CC. Biosanitarias, Universidad Francisco de Vitoria, Ctra. 28223 Madrid, Spain.

出版信息

Int J Oncol. 2005 Dec;27(6):1617-23.

Abstract

Doxazosin is a quinazoline-based compound acting as an alpha-1-adrenergic inhibitor shown to induce apoptosis in prostate cancer cell lines via an alpha-1-adrenergic receptor-independent mechanism. To better understand the mechanism of doxazosin-induced apoptosis in prostate cancer, we performed cDNA microarray to analyze gene expression changes produced by doxazosin in the androgen-dependent human prostate cancer cell line, LNCaP. We found that 70 and 92 genes were deregulated after 8 and 24 h of doxazosin treatment, respectively. These genes are involved in several cellular processes such as cell-cycle regulation, cell adhesion and signal transduction pathways. Strikingly, we found that doxazosin induces deregulation of genes implicated in DNA replication and repair, such as GADD45A, XRCC5 and PRKDC. These facts, together with the demonstration of the ability of doxazosin to bind DNA, allowed us to propose a novel mechanism of action for doxazosin in prostate cancer cells that implies DNA-damage mediated apoptosis by down-regulation of XRCC5 and PRKDC genes.

摘要

多沙唑嗪是一种基于喹唑啉的化合物,作为一种α-1肾上腺素能抑制剂,已显示可通过α-1肾上腺素能受体非依赖性机制诱导前列腺癌细胞系凋亡。为了更好地理解多沙唑嗪诱导前列腺癌凋亡的机制,我们进行了cDNA微阵列分析,以分析多沙唑嗪在雄激素依赖性人前列腺癌细胞系LNCaP中产生的基因表达变化。我们发现,多沙唑嗪处理8小时和24小时后,分别有70个和92个基因的表达发生了改变。这些基因参与了多个细胞过程,如细胞周期调控、细胞黏附和信号转导通路。引人注目的是,我们发现多沙唑嗪会导致参与DNA复制和修复的基因失调,如GADD45A、XRCC5和PRKDC。这些事实,再加上多沙唑嗪能够结合DNA的证据,使我们提出了一种多沙唑嗪在前列腺癌细胞中的新作用机制,即通过下调XRCC5和PRKDC基因介导DNA损伤诱导凋亡。

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