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研究受干扰的核苷代谢和细胞周期,以阐明白藜芦醇对人肺腺上皮细胞的细胞毒性作用。

Investigation into perturbed nucleoside metabolism and cell cycle for elucidating the cytotoxicity effect of resveratrol on human lung adenocarcinoma epithelial cells.

机构信息

State Key Laboratory of Quality Research in Chinese Medicines and Macau Institute for Applied Research in Medicine and Health, Macau University of Science and Technology, Macau 999078, China.

Faculty of Medicine, Macau Institute for Applied Research in Medicine and Health, Macau University of Science and Technology, Macau 999078, China.

出版信息

Chin J Nat Med. 2019 Aug;17(8):608-615. doi: 10.1016/S1875-5364(19)30063-9.

Abstract

In an effort to understand the molecular events contributing to the cytotoxicity activity of resveratrol (RSV), we investigated its effects on human lung adenocarcinoma epithelial cell line A549 at different concentrations. Cellular nucleoside metabolic profiling was determined by an established liquid chromatography-mass spectrometry method in A549 cells. RSV resulted in significant decreases and imbalances of deoxyribonucleoside triphosphates (dNTPs) pools suppressing subsequent DNA synthesis. Meanwhile, RSV at high concentration caused significant cell cycle arrest at S phase, in which cells required the highest dNTPs supply than other phases for DNA replication. The inhibition of DNA synthesis thus blocked subsequent progression through S phase in A549 cells, which may partly contribute to the cytotoxicity effect of RSV. However, hydroxyurea (HU), an inhibitor of RNR activity, caused similar dNTPs perturbation but no S phase arrest, finally no cytotoxicity effect. Therefore, we believed that the dual effect of high concentration RSV, including S phase arrest and DNA synthesis inhibition, was required for its cytotoxicity effect on A549 cells. In summary, our results provided important clues to the molecular basis for the anticancer effect of RSV on epithelial cells.

摘要

为了研究白藜芦醇(Resveratrol,RSV)发挥细胞毒性的分子机制,我们在不同浓度下研究了 RSV 对人肺腺癌细胞系 A549 的作用。采用已建立的液相色谱-质谱法对 A549 细胞中的细胞核苷代谢物进行了分析。结果表明 RSV 导致脱氧核苷三磷酸(dNTP)池显著减少和失衡,从而抑制了随后的 DNA 合成。同时,高浓度 RSV 导致细胞周期在 S 期停滞,而 S 期是细胞进行 DNA 复制时对 dNTP 需求量最大的阶段。因此,DNA 合成的抑制阻止了 A549 细胞随后进入 S 期,这可能是 RSV 发挥细胞毒性作用的部分原因。然而,核糖核苷酸还原酶(RNR)活性抑制剂羟基脲(HU)引起了类似的 dNTP 紊乱,但没有 S 期停滞,最终也没有细胞毒性作用。因此,我们认为 RSV 的高浓度具有双重作用,包括 S 期停滞和 DNA 合成抑制,这是其对 A549 细胞产生细胞毒性作用的必要条件。综上所述,我们的研究结果为 RSV 对上皮细胞的抗癌作用提供了重要的分子基础。

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