肿瘤坏死因子- α和电离辐射对MCF-7人乳腺癌细胞的细胞毒性和锰超氧化物歧化酶诱导。

Lymphokine and cytokine research Pub Date : 1993-10-01
P S Lin, K C Ho, S J Sung, S Tsai
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引用次数: 0

摘要

肿瘤坏死因子- α (TNF)和电离辐射均可引起活性氧自由基介导的细胞损伤和细胞死亡。因此,TNF和放射治疗的细胞可能比单独使用任何一种药物治疗的细胞遭受更大的损伤。另一方面,TNF或放射治疗可以刺激线粒体超氧化物清除酶锰超氧化物歧化酶(MnSOD)的表达,从而降低两种药物的细胞毒性作用。因此,辐射诱导MnSOD可能干扰TNF的细胞毒性作用,反之亦然。我们使用人乳腺肿瘤细胞系MCF-7来测定TNF和辐射对细胞毒性和MnSOD表达的相互作用。肿瘤坏死因子被发现在放疗前使用比放疗后使用更有效。这些观察结果表明,辐射诱导的MnSOD在降低TNF的细胞毒性作用方面更有效,而TNF诱导的MnSOD在抵消辐射作用方面效果较差。我们的研究结果不仅强调了肿瘤坏死因子与放射治疗顺序的不同效果,而且指出了乳腺肿瘤放射治疗的潜在意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cytotoxicity and manganese superoxide dismutase induction by tumor necrosis factor-alpha and ionizing radiation in MCF-7 human breast carcinoma cells.

Both tumor necrosis factor-alpha (TNF) and ionizing radiation cause active-oxygen radical-mediated cell injuries and cell death. Thus cells treated by both TNF and radiation may suffer greater injuries than cells treated by either agent alone. On the other hand, TNF or radiation treatment can stimulate the expression of a mitochondrial superoxide scavenging enzyme, manganese superoxide dismutase (MnSOD), which can lower the cytotoxic effects of both agents. Thus, the induction of MnSOD by radiation may interfere with the cytotoxic action of TNF and vice versa. We used a human breast tumor cell line, MCF-7, to determine the interaction of TNF and radiation on cytotoxicity and MnSOD expression. TNF was found to be more effective as a cytotoxic agent when used before than after radiation treatment. These observations suggest that radiation induced-MnSOD was more effective in reducing the cytotoxic effect of TNF whereas TNF induction of MnSOD was less effective in counteracting the radiation action. Our results not only underscore the different effects of the treatment order of TNF and radiation, but also point to potential implication in the radiotherapy of breast tumors.

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