UMR CNRS 7213, Laboratoire de Biophotonique et Pharmacologie, Faculté de Pharmacie, Université de Strasbourg, 74 Route du Rhin, CS 60024, Illkirch, Cedex F-67401, France.
J Exp Clin Cancer Res. 2013 May 20;32(1):30. doi: 10.1186/1756-9966-32-30.
Several reports have described the potential effects of natural compounds as anti-cancer agents in vitro as well as in vivo. The aim of this study was to evaluate the anti-cancer effect of Limoniastrum guyonianum aqueous gall extract (G extract) and luteolin in the human cervical cancer HeLa cell line, and, if so, to clarify the underlying mechanism. Our results show that G extract and luteolin inhibited cell proliferation and induced G2/M cell cycle arrest in a concentration and time-dependent manner. Both natural products induced programmed cell death as confirmed by the presence of hypodiploid G0/G1 cells. These effects are associated with an up-regulation of the expression of the tumor suppressor gene p16INK4A and a down-regulation of the expression of the anti-apoptotic actor UHRF1 and its main partner DNMT1. Moreover, G extract- and luteolin-induced UHRF1 and DNMT1 down-regulation is accompanied with a global DNA hypomethylation in HeLa cell line. Altogether our results show that G extract mediates its growth inhibitory effects on human cervical cancer HeLa cell line likely via the activation of a p16INK4A-dependent cell cycle checkpoint signalling pathway orchestrated by UHRF1 and DNMT1 down-regulation.
已有多项报告描述了天然化合物作为体外及体内抗癌剂的潜在作用。本研究旨在评估芫花素水提醇沉物(G 提取物)和木犀草素对人宫颈癌 HeLa 细胞系的抗癌作用,并阐明其潜在机制。我们的结果表明,G 提取物和木犀草素可浓度和时间依赖性地抑制细胞增殖并诱导 G2/M 细胞周期阻滞。两种天然产物均诱导细胞程序性死亡,这可通过存在亚二倍体 G0/G1 细胞得到证实。这些作用与肿瘤抑制基因 p16INK4A 的表达上调和抗凋亡因子 UHRF1 及其主要伴侣 DNMT1 的表达下调相关。此外,G 提取物和木犀草素诱导的 UHRF1 和 DNMT1 下调与 HeLa 细胞系中的全基因组 DNA 低甲基化有关。总之,我们的研究结果表明,G 提取物可能通过激活 p16INK4A 依赖性细胞周期检查点信号通路,介导对人宫颈癌 HeLa 细胞系的生长抑制作用,该通路由 UHRF1 和 DNMT1 的下调来调控。