Kim Chang Jae, Cho Yong Gu, Park Cho Hyun, Jeong Seong Whan, Nam Suk Woo, Kim Su Young, Lee Sug Hyung, Yoo Nam Jin, Lee Jung Young, Park Won Sang
Department of Pathology, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Oncogene. 2004 Nov 11;23(53):8591-6. doi: 10.1038/sj.onc.1208113.
SIAH-1: is the mammalian homolog of Drosophila seven in absentia (sina) and has been identified as a p53-inducible gene. Siah-1 can induce cell cycle arrests, tumor suppression, and apoptosis through a novel beta-catenin degradation pathway. To determine whether genetic alterations of Siah-1 gene are involved in the development and/or progression of gastric cancer, we searched for mutation of the Siah-1 gene in 95 gastric cancers by single-strand conformational polymorphism and sequencing. The effect of Siah-1 on beta-catenin degradation was further examined in wild- and mutant-type Siah-1-transfected HEK 293T cells. We found two missense mutations of the Siah-1 gene. The cases with Siah-1 mutation showed nuclear translocation and cytoplasmic staining of beta-catenin. Interestingly, two mutants of Siah-1 stabilized cytoplasmic levels of beta-catenin, even after treatment of adriamycin. Furthermore, both mutants failed to suppress cyclin D1 expression and to induce apoptosis. These data suggest that inactivating mutations of the Siah-1 may contribute to the development of gastric cancer through beta-catenin stabilization and apoptosis block.
SIAH-1:是果蝇无七(sina)在哺乳动物中的同源物,已被鉴定为一种p53诱导基因。Siah-1可通过一种新的β-连环蛋白降解途径诱导细胞周期停滞、肿瘤抑制和细胞凋亡。为了确定Siah-1基因的遗传改变是否参与胃癌的发生和/或发展,我们通过单链构象多态性和测序在95例胃癌中寻找Siah-1基因的突变。在野生型和突变型Siah-1转染的HEK 293T细胞中进一步检测Siah-1对β-连环蛋白降解的影响。我们发现了Siah-1基因的两个错义突变。发生Siah-1突变的病例显示β-连环蛋白的核转位和细胞质染色。有趣的是,即使在阿霉素处理后,Siah-1的两个突变体仍能稳定β-连环蛋白的细胞质水平。此外,这两个突变体均未能抑制细胞周期蛋白D1的表达并诱导细胞凋亡。这些数据表明,Siah-1的失活突变可能通过β-连环蛋白稳定和凋亡阻滞促进胃癌的发生。