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全反式维甲酸和三氧化二砷可诱导肝癌细胞凋亡并调节其细胞内钙浓度。

All-trans retinoic acid and arsenic trioxide induce apoptosis and modulate intracellular concentrations of calcium in hepatocellular carcinoma cells.

作者信息

Wei Jianfeng, Ye Chaoping, Liu Fengsheng, Wang Wenqing

出版信息

J Chemother. 2014 Dec;26(6):348-52. doi: 10.1179/1973947814Y.0000000200. Epub 2014 Jul 28.

Abstract

We investigated the effects of all-trans retinoic acid (ATRA) and arsenic trioxide (ATO), alone and in combination, on apoptosis and intracellular calcium concentration in hepatocellular carcinoma (HepG2) cells. We used HepG2 cells to test the effects of ATRA and ATO, individually and in combination, on cell proliferation, apoptosis, and intracellular-free calcium concentration. The results indicate that each drug decreased cell proliferation, increased apoptosis, and increased intracellular-free calcium in a time- and dose-dependent manner. We also calculated the coefficients of drug interaction for sub-threshold administration of both drugs in combination (1 μmol/L each). ATRA and ATO acted synergistically in inhibition of cell proliferation and additively in the promotion of apoptosis. All-trans retinoic acid and ATO interacted synergistically to reduce cell proliferation in HepG2 cells.

摘要

我们研究了全反式维甲酸(ATRA)和三氧化二砷(ATO)单独及联合使用对肝癌(HepG2)细胞凋亡和细胞内钙浓度的影响。我们使用HepG2细胞来测试ATRA和ATO单独及联合使用对细胞增殖、凋亡和细胞内游离钙浓度的影响。结果表明,每种药物均以时间和剂量依赖性方式降低细胞增殖、增加凋亡并提高细胞内游离钙水平。我们还计算了两种药物联合亚阈值给药(每种1 μmol/L)时的药物相互作用系数。ATRA和ATO在抑制细胞增殖方面协同作用,在促进凋亡方面相加作用。全反式维甲酸和ATO协同作用以减少HepG2细胞的增殖。

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