Brefeldin a诱导人前列腺癌细胞生长抑制和细胞死亡的机制。

Molecular urology Pub Date : 1999-01-01
Chapman, Tazaki, Mallouh, Konno
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摘要

研究了brefeldin A (BFA)在人前列腺癌DU-145细胞中抑制生长和引发细胞死亡的机制。用不同浓度的BFA培养细胞后,在指定时间测定细胞数量和活力。与未处理的细胞相比,在BFA (30 ng/mL)培养72小时的细胞中观察到生长急剧减少(>80%),约50%的细胞死亡。使用流式细胞术进行细胞周期分析显示,这种生长抑制与s期群体减少约85%相关,表明抑制G(1)-S期进展。Western blots进一步显示,细胞周期依赖性激酶(cdk2和cdk4)、细胞周期蛋白D(1)和p53均下调,而WAF1 (p21)在BFA处理下上调。通过TUNEL法和琼脂糖凝胶电泳法对BFA诱导细胞凋亡的可能性进行了评估。TUNEL实验显示bfa处理的细胞呈阳性染色,凝胶电泳证实核小体DNA形成阶梯。因此,这些结果表明,BFA对DU-145细胞的生长抑制主要归因于通过调节特定的细胞周期调节剂使G1细胞周期停滞。伴随的细胞死亡可能遵循不依赖p53的凋亡途径。
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Mechanism of Brefeldin A-Induced Growth Inhibition and Cell Death in Human Prostatic Carcinoma Cells.

The mechanism of growth inhibition and triggering of cell death by the antibiotic brefeldin A (BFA) was investigated in human prostatic cancer DU-145 cells. After cells were cultured with various concentrations of BFA, cell number and viability were determined at specified times. Compared with untreated cells, a drastic growth reduction (>80%) with approximately 50% cell death was observed in the cells cultured with BFA (30 ng/mL) for 72 h. Cell-cycle analysis using flow cytometry revealed that such growth inhibition was associated with approximately 85% reduction in the S-phase population, indicating the inhibition of the G(1)-S phase progression. Western blots further showed that cell-cycle-dependent kinases (cdk2 and cdk4), cyclin D(1), and p53 were all downregulated, whereas WAF1 (p21) was upregulated with BFA treatment. Possible induction of apoptosis by BFA was also assessed by TUNEL assay and by DNA analysis using agarose gel electrophoresis. The TUNEL assay demonstrated the positive staining of BFA-treated cells, and gel electrophoresis confirmed nucleosomal DNA ladder formation. Thus, these results suggest that growth inhibition of DU-145 cells by BFA is attributable mainly to a G1 cell-cycle arrest through the modulation of specific cell-cycle regulators. The accompanying cell death may follow a p53-independent apoptotic pathway.

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