Cancer Research Institute, The Catholic University of Korea, 505 Banpo-dong, Seocho-gu, Seoul 137-040, Korea.
Nutr Res Pract. 2008 Winter;2(4):322-5. doi: 10.4162/nrp.2008.2.4.322. Epub 2008 Dec 31.
The aim of present study was to investigate the effects of kaempferol on cellular proliferation and cell cycle arrest and explore the mechanism for these effects in human breast carcinoma MDA-MB-453 cells. Cells were treated with kaempferol at various concentrations (ranging from 1 to 200 microM) for 24 and 48 hrs. Kaempferol significantly inhibited cancer cell growth in cells exposed to 50 and 10 microM of kaempferol and incubated for 24 and 48 hrs, respectively. Exposure to kaempferol resulted in cell cycle arrest at the G2/M phase. Of the G2/M-phase related proteins, kaempferol down-regulated CDK1 and cyclin A and B in cells exposed to kaempferol. In addition, small DNA fragments at the sub-G0 phase were increased by up to 23.12 and 31.90% at 10 and 50 microM incubated for 24 and 48 hrs, respectively. The kaempferol-induced apoptosis was associated with the up-regulation of p53. In addition, the phosphorylation of p53 at the Ser-15 residue was observed with kaempferol. Kaempferol inhibits cell proliferation by disrupting the cell cycle, which is strongly associated with the induction of arrest at G2/M phase and may induce apoptosis via p53 phosphorylation in human breast carcinoma MDA-MB-453 cells.
本研究旨在探讨山柰酚对细胞增殖和细胞周期阻滞的影响,并探讨其在人乳腺癌 MDA-MB-453 细胞中的作用机制。将细胞用山柰酚在不同浓度(1 至 200 μM)下处理 24 和 48 小时。山柰酚显著抑制了暴露于 50 和 10 μM 山柰酚并孵育 24 和 48 小时的癌细胞生长。暴露于山柰酚导致细胞周期在 G2/M 期停滞。在暴露于山柰酚的细胞中,G2/M 期相关蛋白 CDK1 和细胞周期蛋白 A 和 B 下调。此外,在 10 和 50 μM 孵育 24 和 48 小时时,小 DNA 片段在亚 G0 期增加了 23.12%和 31.90%。山柰酚诱导的细胞凋亡与 p53 的上调有关。此外,用山柰酚观察到 p53 在 Ser-15 残基上的磷酸化。山柰酚通过破坏细胞周期抑制细胞增殖,这与 G2/M 期阻滞的诱导密切相关,并且可能通过人乳腺癌 MDA-MB-453 细胞中 p53 的磷酸化诱导细胞凋亡。