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苦味叶下珠提取物对5-氟尿嘧啶诱导的HepG2细胞系核糖核苷酸和脱氧核糖核苷酸库紊乱的影响。

Effect of Phyllanthus amarus Extract on 5-Fluorouracil-Induced Perturbations in Ribonucleotide and Deoxyribonucleotide Pools in HepG2 Cell Line.

作者信息

Guo Jian-Ru, Chen Qian-Qian, Lam Christopher Wai-Kei, Wang Cai-Yun, Xu Feng-Guo, Liu Bu-Ming, Zhang Wei

机构信息

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

Key Laboratory of Drug Quality Control and Pharmacovigilance (Ministry of Education), China Pharmaceutical University, Nanjing 210009, China.

出版信息

Molecules. 2016 Sep 20;21(9):1254. doi: 10.3390/molecules21091254.

Abstract

The aim of this study was to investigate the antitumor activities of (PHA) and its potential of herb-drug interactions with 5-Fluorouracil (5-FU). Cell viability, ribonucleotides (RNs) and deoxyribonucleotides (dRNs) levels, cell cycle distribution, and expression of thymidylate synthase (TS) and ribonucleotide reductase (RR) proteins were measured with 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, high performance liquid chromatography tandem mass spectrometry (HPLC/MS/MS) method, flow cytometry and Western blot analysis, respectively. Our standardized PHA extract showed toxicity to HepG2 cells at high concentrations after 72 h exposure and induced G2/M cell cycle arrest. Combined use of 5-FU with PHA resulted in significant decreases in ATP, CTP, GTP, UTP and dTTP levels, while AMP, CMP, GMP and dUMP levels increased significantly compared with use of 5-FU alone. Further, PHA could increase the role of cell cycle arrest at S phase induced by 5-FU. Although PHA alone had no direct impact on TS and RR, PHA could change the levels of RNs and dRNs when combined with 5-FU. This may be due to cell cycle arrest or regulation of key enzyme steps in intracellular RNs and dRNs metabolism.

摘要

本研究旨在探讨商陆抗病毒蛋白(PHA)的抗肿瘤活性及其与5-氟尿嘧啶(5-FU)的药物相互作用潜力。分别采用3-(4,5-二甲基噻唑-2)-2,5-二苯基四氮唑溴盐(MTT)法、高效液相色谱串联质谱(HPLC/MS/MS)法、流式细胞术和蛋白质免疫印迹分析,测定细胞活力、核糖核苷酸(RNs)和脱氧核糖核苷酸(dRNs)水平、细胞周期分布以及胸苷酸合成酶(TS)和核糖核苷酸还原酶(RR)蛋白的表达。我们的标准化PHA提取物在72小时暴露后对高浓度的HepG2细胞显示出毒性,并诱导G2/M期细胞周期阻滞。5-FU与PHA联合使用导致ATP、CTP、GTP、UTP和dTTP水平显著降低,而与单独使用5-FU相比,AMP、CMP、GMP和dUMP水平显著升高。此外,PHA可以增强5-FU诱导的S期细胞周期阻滞作用。虽然单独使用PHA对TS和RR没有直接影响,但PHA与5-FU联合使用时可以改变RNs和dRNs的水平。这可能是由于细胞周期阻滞或细胞内RNs和dRNs代谢关键酶步骤的调节所致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3228/6273671/14ca4cb5b1c6/molecules-21-01254-g001.jpg

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