Department of Molecular-Targeting Cancer Prevention, Kyoto Prefectural University of Medicine, Kamigyo-ku, Kyoto, Japan.
Int J Oncol. 2012 Mar;40(3):816-24. doi: 10.3892/ijo.2011.1246. Epub 2011 Oct 27.
The phosphatidylinositol 3-kinase (PI3K) signaling pathway is activated in a broad spectrum of human cancers, including colon cancer. The natural product brassinin is a type of indole compound derived from cruciferous vegetables, and has been shown to have anti-proliferative effects against cancer for both in vivo and in vitro models. Here, we show for the first time that brassinin inhibits cell growth in human colon cancer cells by arresting the cell cycle at the G1 phase via inhibition of the PI3K signaling pathway. Brassinin increased the expression of p21 and p27, resulting in hypophosphorylation of the retinoblastoma gene (RB). Knockdown of p21 or p27 by each siRNA significantly repressed G1 phase arrest induced by brassinin. The increase of p21 and p27 was associated with inhibition of the PI3K signaling pathway. In addition, exogenous expression of constitutively active Akt represses the cell cycle arrest at G1 phase induced by brassinin. These results suggest the possibility that brassinin inhibits the PI3K signaling pathway and upregulates the expression of p21 and p27, thereby inducing G1 phase arrest.
磷脂酰肌醇 3-激酶 (PI3K) 信号通路在包括结肠癌在内的广泛人类癌症中被激活。天然产物 brassinin 是一种吲哚类化合物,来源于十字花科蔬菜,已被证明对体内和体外模型中的癌症具有抗增殖作用。在这里,我们首次表明 brassinin 通过抑制 PI3K 信号通路使细胞周期在 G1 期停滞,从而抑制人结肠癌细胞的生长。Brassinin 增加了 p21 和 p27 的表达,导致视网膜母细胞瘤基因 (RB) 的低磷酸化。每种 siRNA 对 p21 或 p27 的敲低显着抑制了 brassinin 诱导的 G1 期阻滞。p21 和 p27 的增加与 PI3K 信号通路的抑制有关。此外,组成型激活 Akt 的外源性表达抑制了 brassinin 诱导的 G1 期阻滞。这些结果表明 brassinin 可能通过抑制 PI3K 信号通路和上调 p21 和 p27 的表达,从而诱导 G1 期阻滞。