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首页> 外文期刊>Molecular and Cellular Biochemistry: An International Journal for Chemical Biology >Enhancement in alpha-tocopherol succinate-induced apoptosis by all-trans-retinoic acid in primary leukemic cells: role of antioxidant defense, Bax and c-myc.
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Enhancement in alpha-tocopherol succinate-induced apoptosis by all-trans-retinoic acid in primary leukemic cells: role of antioxidant defense, Bax and c-myc.

机译:全反式维甲酸在原代白血病细胞中增强α-生育酚琥珀酸酯诱导的细胞凋亡:抗氧化剂防御,Bax和c-myc的作用。

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摘要

We investigated the possible mechanisms of All-trans retinoic acid (ATRA)-promoted apoptosis induced by alpha-tocopherol succinate (alpha-TS) in freshly isolated leukemic cells obtained from chronic myeloid leukemic patients. alpha-TS at 50 microM concentration significantly decreased superoxide dismutase (SOD) activity and reduced glutathione (GSH) by 29% and 25%, respectively, and increased lipid peroxidation level by 33%. Though 10 microM ATRA did not affect these parameters, it further significantly enhanced alpha-TS-induced changes. Bax expression in the leukemic cells was increased by treatment with ATRA, alpha-TS, and their combination to 40%, 240%, and 320%, respectively, without any change in Bcl2 and p53 expression. C-myc was down regulated by treatment with ATRA, alpha-TS and their combination to 22%, 48.5%, and 52%, respectively. In conclusion, the data reveal that enhancement of alpha-TS-induced apoptosis by ATRA in leukemic cells was through up regulation of Bax and lipid peroxidation, and down regulation of c-myc and GSH.
机译:我们调查了全反式维甲酸(ATRA)促进由α-生育酚琥珀酸酯(α-TS)诱导的从慢性粒细胞白血病患者获得的新鲜分离的白血病细胞中诱导凋亡的可能机制。浓度为50 microM的alpha-TS分别显着降低了超氧化物歧化酶(SOD)活性,并使谷胱甘肽(GSH)降低了29%和25%,脂质过氧化水平提高了33%。尽管10 microM ATRA不会影响这些参数,但它进一步显着增强了α-TS诱导的变化。通过用ATRA,α-TS及其组合治疗,白血病细胞中的Bax表达分别增加到40%,240%和320%,而Bcl2和p53表达没有任何变化。通过ATRA,α-TS及其组合治疗,C-myc分别下调至22%,48.5%和52%。总之,数据表明白血病细胞中ATRA增强α-TS诱导的凋亡是通过上调Bax和脂质过氧化作用,以及下调c-myc和GSH来实现的。

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