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Superoxide dismutase as a target enzyme for Fe-porphyrin-induced cell death

机译:超氧化物歧化酶作为铁卟啉诱导的细胞死亡的靶酶

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摘要

The cell viability of human cancer cell lines treated with [5,10-bis(N-methyl-4-pyridyl)-15,20-diphenyl]porphinatoiron(III) (cis-FeM-Py2P2P) has been estimated. The cis-FeMPy2P2P is a superoxide dismutase (SOD) mimic in vitro that exhibited a significant toxicity in cancer cell lines. This toxicity is rather due to pro-oxidant properties of the iron-porphyrin in vivo. We have demonstrated that there was the relationship between the LD50 values calculated from the viability of cancer cell lines treated with cis-FeMPy2P2P and the SOD activities of the cell lines. Furthermore, the inhibition of SOD by antisense S-oligonucleotide increased the cytotoxic effect of cis-FeMPy2P2P against cancer cells. These results suggest that SOD is a target enzyme for the cell death induced by cis-FeMPy2P2P as a new class of anticancer agents. (c) 2006 Elsevier Inc. All rights reserved.
机译:已经估计了用[5,10-双(N-甲基-4-吡啶基)-15,20-二苯基]卟啉铁(III)(cis-FeM-Py2P2P)处理的人癌细胞的细胞生存力。 cis-FeMPy2P2P是一种体外模拟的超氧化物歧化酶(SOD),在癌细胞系中表现出明显的毒性。该毒性实际上是由于体内卟啉铁的促氧化特性所致。我们已经证明,从用顺式-FeMPy2P2P处理的癌细胞系的生存力计算出的LD50值与细胞系的SOD活性之间存在关系。此外,反义S-寡核苷酸对SOD的抑制作用增强了顺式FeMPy2P2P对癌细胞的细胞毒性作用。这些结果表明,SOD是由顺式FeMPy2P2P作为一类新的抗癌剂诱导的细胞死亡的靶酶。 (c)2006 Elsevier Inc.保留所有权利。

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