Am J Transl Res. 2011;3(5):479-91. Epub 2011 Oct 13.
The gold (III) porphyrin complex, gold-2a, elicits anti-tumor activity by targeting the Wnt/β-catenin signaling pathway [Chow KH et al, Cancer Research 2010;70(1):329-37]. Here, the molecular mechanisms underlying the inhibitory effects of this compound on WNT1 gene expression were elucidated further. A response element to gold-2a was identified located within the -1290 to -1112 nt region of the WNT1 promoter, containing a binding site for the transcription regulator Yin Yang 1 (YY1). Gold-2a promoted the association of YY1 and suppressor of zeste 12 (Suz12; a component of the polycomb repressor complex 2) with the WNT1 promoter. Under normal culture conditions, the intracellular translocalization of YY1 was synchronized with cell cycle progression and WNT1 expression. Gold-2a promoted the nuclear accumulation and abolished the nuclear exportation of YY1, resulting in a persistent inhibition of WNT1 expression and a cell cycle arrest at G1/S phase. A dimorphic role of YY1 in regulating cell proliferation and division was revealed. Thus, the present study extends the understanding of the anti-tumor mechanism of gold-2a to the epigenetic level, which involves the modulation of the dynamic interactions between YY1 and a specific region of the WNT1 promoter.
金(III)卟啉配合物金-2a 通过靶向 Wnt/β-catenin 信号通路发挥抗肿瘤活性[Chow KH 等人,Cancer Research 2010;70(1):329-37]。在此,进一步阐明了该化合物对 WNT1 基因表达的抑制作用的分子机制。鉴定出位于 WNT1 启动子的-1290 至-1112nt 区域内的金-2a 反应元件,该元件包含转录调节剂 Yin Yang 1(YY1)的结合位点。金-2a 促进 YY1 和抑制 zeste 12(Suz12;多梳抑制复合物 2 的一个组成部分)与 WNT1 启动子的结合。在正常培养条件下,YY1 的细胞内易位与细胞周期进程和 WNT1 表达同步。金-2a 促进 YY1 的核积累并消除其核输出,导致 WNT1 表达持续抑制和细胞周期在 G1/S 期停滞。揭示了 YY1 在调节细胞增殖和分裂中的双相作用。因此,本研究将金-2a 的抗肿瘤机制扩展到涉及 YY1 与 WNT1 启动子特定区域之间动态相互作用的表观遗传水平。