Key Lab of Combined Multi-Organ Transplantation, Ministry of Public Health, First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310003, Zhejiang Province, China.
Biochem Biophys Res Commun. 2012 Mar 30;420(1):29-35. doi: 10.1016/j.bbrc.2012.02.107. Epub 2012 Feb 27.
Cyclin-dependent kinase inhibitor 3 (CDKN3) belongs to the protein phosphatases family and has a dual function in cell cycling. The function of this gene has been studied in several kinds of cancers, but its role in human hepatocellular carcinoma (HCC) remains to be elucidated. In this study, we found that CDKN3 was frequently overexpressed in both HCC cell lines and clinical samples, and this overexpression was correlated with poor tumor differentiation and advanced tumor stage. Functional studies showed that overexpression of CDKN3 could promote cell proliferation by stimulating G1-S transition but has no impact on cell apoptosis and invasion. Microarray-based co-expression analysis identified a total of 61 genes co-expressed with CDKN3, with most of them involved in cell proliferation, and BIRC5 was located at the center of CDKN3 co-expression network. These results suggest that CDKN3 acts as an oncogene in human hepatocellular carcinoma and antagonism of CDKN3 may be of interest for the treatment of HCC.
细胞周期蛋白依赖性激酶抑制剂 3(CDKN3)属于蛋白磷酸酶家族,在细胞周期中具有双重功能。该基因的功能已在多种癌症中进行了研究,但它在人肝细胞癌(HCC)中的作用仍有待阐明。在这项研究中,我们发现 CDKN3 在 HCC 细胞系和临床样本中经常过度表达,这种过表达与肿瘤分化不良和肿瘤分期较晚有关。功能研究表明,CDKN3 的过表达可以通过刺激 G1-S 转换来促进细胞增殖,但对细胞凋亡和侵袭没有影响。基于微阵列的共表达分析共鉴定出与 CDKN3 共表达的 61 个基因,其中大多数基因与细胞增殖有关,BIRC5 位于 CDKN3 共表达网络的中心。这些结果表明 CDKN3 是人肝细胞癌中的一种癌基因,拮抗 CDKN3 可能对 HCC 的治疗有意义。