Department of Cell Biology, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.
Anticancer Res. 2012 Jun;32(6):2301-8.
Oncogenic KRAS signaling is dysregulated in a three-dimensional (3D)-specific manner in human colorectal cancer (CRC) HCT116 cells. However, the identity of the crucial genes which are down-regulated through oncogenic KRAS in 3D cultures remains unclear.
We established a specific anti-alpha-kinase 2 (ALPK2) antibody and addressed the ALPK2 function in HKe3 cells, which are HCT116 cells with a disruption in oncogenic KRAS, in a 3D colonic-crypt model.
In HKe3 cells grown in 3D culture, ALPK2 siRNA inhibited luminal apoptosis and reduced the expression of cleaved caspase-3. Furthermore, ALPK2 siRNA reduced the expression of DNA repair genes. Reduced expression of ALPK2 mRNA was found to be correlated with clinical colorectal adenomas in a public dataset of gene expression analyses.
ALPK2, down-regulated by oncogenic KRAS, is crucial for luminal apoptosis and expression of DNA repair-related genes, possibly in the transition of normal colonic crypt to adenoma.
在人类结直肠癌细胞(CRC)HCT116 中,致癌性 KRAS 信号以三维(3D)特异性方式失调。然而,通过致癌性 KRAS 在 3D 培养物中下调的关键基因的身份仍然不清楚。
我们建立了一种特异性的抗α-激酶 2(ALPK2)抗体,并在具有致癌性 KRAS 缺失的 HKe3 细胞中解决了 3D 结肠隐窝模型中的 ALPK2 功能。
在 3D 培养中生长的 HKe3 细胞中,ALPK2 siRNA 抑制腔凋亡并减少裂解 caspase-3 的表达。此外,ALPK2 siRNA 降低了 DNA 修复基因的表达。在一个公共的基因表达分析数据集,发现 ALPK2 mRNA 的表达降低与临床结直肠腺瘤相关。
由致癌性 KRAS 下调的 ALPK2 对于腔凋亡和 DNA 修复相关基因的表达至关重要,可能在正常结肠隐窝向腺瘤的转化中起作用。