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Reversal of Tumor Necrosis Factor Resistance in Tumor Cells by Adriamycin via Suppression of Intracellular Resistance Factors

机译:阿霉素通过抑制细胞内抗性因子逆转肿瘤细胞中的肿瘤坏死因子抗性

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摘要

Tumor necrosis factor (TNF) and various chemotherapeutic drugs show synergistic antitumor effects in vitro and in vivo, though the mechanism is not clear. Based on our previous finding that endogenous TNF (enTNF) acts as an intracellular resistance factor against exogenous TNF by scavenging oxygen free radicals (OFR) with induced manganous superoxide dismutase (MnSOD), we examined the suppression of these resistance factors by chemotherapeutic drugs and the resulting increase in TNF cytotoxicity. Pretreatment of HeLa cells, which produce an appreciable amount of enTNF and show apparent TNF resistance, with TNF followed by adriamycin (ADM) resulted in an additive effect, whereas pretreatment with ADM followed by TNF resulted in a synergistic effect. After treatment of HeLa cells with ADM, the expression of enTNF was remarkably suppressed and MnSOD activity was decreased by one‐half. These results indicate that suppression of the intracellular resistance factors, i.e., enTNF and MnSOD, by ADM plays an important role in the mechanism of the synergistic antitumor effect of TNF in combination with ADM.
机译:肿瘤坏死因子(TNF)和各种化学治疗药物在体内和体外显示出协同的抗肿瘤作用,尽管机理尚不清楚。基于我们先前的发现,即内源性TNF(enTNF)通过诱导锰超氧化物歧化酶(MnSOD)清除氧自由基(OFR)来充当针对外源性TNF的细胞内耐药因子,我们研究了化学疗法药物和这些药物对这些耐药因子的抑制作用。导致TNF细胞毒性增加。 TNF继之以阿霉素(ADM)预处理产生大量enTNF并表现出明显的TNF抵抗力的HeLa细胞进行预处理可产生累加效应,而ADM继之以TNF预处理则产生协同作用。用ADM处理HeLa细胞后,enTNF的表达被显着抑制,而MnSOD活性降低了一半。这些结果表明,ADM抑制细胞内抗性因子,即enTNF和MnSOD在与ADM结合的TNF的协同抗肿瘤作用机理中起重要作用。

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