Shah Gopitkumar, Zielonka Jacek, Chen Fanghong, Zhang Guangjian, Cao YanLi, Kalyanaraman Balaraman, See William
Departments of Urology and Biophysics (JZ, BK), Medical College of Wisconsin, Milwaukee, Wisconsin.
J Urol. 2014 Oct;192(4):1238-48. doi: 10.1016/j.juro.2014.05.115. Epub 2014 Jun 10.
Exposure of urothelial carcinoma cells to bacillus Calmette-Guérin affects cellular redox status and tumor cell biology but the mechanism(s) remain unclear. We examined free radical production by bacillus Calmette-Guérin in tumor cells in response to the bacillus using global profiling of reactive oxygen species/reactive nitrogen species. The relationship between free radical generation and downstream cellular events was evaluated.
Using fluorescent probes we performed global profiling of reactive oxygen species/reactive nitrogen species in heat killed and viable bacillus Calmette-Guérin, and in the 253J and T24 urothelial carcinoma cell lines after exposure to the bacillus. Inhibition of bacillus Calmette-Guérin internalization and H2O2 pharmacological scavenging were studied for their effect on cellular reactive oxygen species/reactive nitrogen species generation and various physiological end points.
Viable bacillus Calmette-Guérin produced H2O2 and O2(-) but nitric oxide was not generated. Loss of viability decreased H2O2 production by 50% compared to viable bacillus. Bacillus Calmette-Guérin internalization was necessary for the bacillus to induce reactive oxygen species/reactive nitrogen species generation in urothelial carcinoma cells. Pharmacological H2O2 scavenging reversed reactive oxygen species/reactive nitrogen species mediated signaling in urothelial carcinoma cells. Bacillus Calmette-Guérin dependent alterations in tumor biology, including intracellular signaling, gene expression and cytotoxicity, depended on free radical generation.
This study demonstrates the importance of free radical generation by bacillus Calmette-Guérin and intracellular generation of cellular oxidative stress on the urothelial carcinoma cell response to the bacillus. Manipulating the cellular oxidative stress induced by bacillus Calmette-Guérin represents a potential target to increase the efficacy of the bacillus.
卡介苗(Bacillus Calmette-Guérin,BCG)作用于尿路上皮癌细胞会影响细胞的氧化还原状态和肿瘤细胞生物学特性,但其机制尚不清楚。我们通过对活性氧/活性氮进行整体分析,研究了卡介苗在肿瘤细胞中产生自由基的情况以及对该细菌的反应。评估了自由基生成与下游细胞事件之间的关系。
我们使用荧光探针,对热灭活和活的卡介苗以及暴露于该细菌后的253J和T24尿路上皮癌细胞系中的活性氧/活性氮进行了整体分析。研究了抑制卡介苗内化和H2O2药物清除对细胞活性氧/活性氮生成及各种生理终点的影响。
活的卡介苗产生H2O2和O2(-),但不产生一氧化氮。与活的卡介苗相比,活力丧失使H2O2产量降低了50%。卡介苗内化对于该细菌诱导尿路上皮癌细胞中活性氧/活性氮生成是必要的。药物清除H2O2可逆转尿路上皮癌细胞中活性氧/活性氮介导的信号传导。卡介苗依赖的肿瘤生物学改变,包括细胞内信号传导、基因表达和细胞毒性,取决于自由基的生成。
本研究证明了卡介苗产生自由基以及细胞内产生氧化应激对尿路上皮癌细胞对该细菌反应的重要性。调控卡介苗诱导的细胞氧化应激是提高该细菌疗效的一个潜在靶点。