Wagner Brett A, Evig Crystal B, Reszka Krzysztof J, Buettner Garry R, Burns C Patrick
Department of Medicine, The University of Iowa Carver College of Medicine and Holden Comprehensive Cancer Center, Iowa City, IA 52242, USA.
Arch Biochem Biophys. 2005 Aug 15;440(2):181-90. doi: 10.1016/j.abb.2005.06.015.
We studied the effect of doxorubicin on the production of hydrogen peroxide by PC3 human prostate cancer cells, using a sensitive assay based on aminotriazole-mediated inhibition of catalase. PC3 cells exposed to increasing concentrations of doxorubicin had an increase in intracellular hydrogen peroxide that was concentration-dependent up to 1 microM doxorubicin. The apparent hydrogen peroxide concentration in the PC3 cells was 13 +/- 4 pM under basal steady-state conditions and increased to 51 +/- 13 pM after exposure to 1 microM doxorubicin for 30 min. The level of hydrogen peroxide in the medium as measured by Amplex Red did not increase as a result of doxorubicin treatment. PC3 cells overexpressing catalase were no more resistant to doxorubicin cytotoxicity as compared to non-transduced wild-type cells; therefore, the exact role of hydrogen peroxide in anthracycline cytotoxicity remains unproven. This study demonstrates that a specific oxidative event associated with the exposure of PC3 human prostate cancer cells to anthracyclines results in an increase in intracellular hydrogen peroxide.
我们使用基于氨基三唑介导的过氧化氢酶抑制的灵敏测定法,研究了阿霉素对PC3人前列腺癌细胞产生过氧化氢的影响。暴露于浓度不断增加的阿霉素的PC3细胞,其细胞内过氧化氢水平升高,在阿霉素浓度达到1微摩尔之前呈浓度依赖性。在基础稳态条件下,PC3细胞中过氧化氢的表观浓度为13±4皮摩尔,在暴露于1微摩尔阿霉素30分钟后增加到51±13皮摩尔。用Amplex Red测定的培养基中过氧化氢水平并未因阿霉素处理而增加。与未转导的野生型细胞相比,过表达过氧化氢酶的PC3细胞对阿霉素细胞毒性并无更强的抗性;因此,过氧化氢在蒽环类药物细胞毒性中的确切作用仍未得到证实。本研究表明,与PC3人前列腺癌细胞暴露于蒽环类药物相关的特定氧化事件会导致细胞内过氧化氢增加。