Author/Authors :
Jung، نويسنده , , Yu-Jin and Lee، نويسنده , , Kee-Ho and Choi، نويسنده , , Dong-Wook and Han، نويسنده , , Chul Ju and Jeong، نويسنده , , Sook-Hyang and Kim، نويسنده , , Keun-Cheol and Oh، نويسنده , , Jong-Won and Park، نويسنده , , Taek-Kyu and Kim، نويسنده , , Chang-Min، نويسنده ,
Abstract :
Deregulation of the cell cycle by overexpression of G1 cyclins, cyclin E and cyclin D1 genes, has been demonstrated to be a prerequisite for the development of human cancer. Recently, cyclin E is proposed to be sufficient for the progression of the G1 cell cycle without cyclin D1. Here we show that the proposed model system was specifically present in human hepatocellular carcinoma (HCC) unlike other human cancers. Of 31 HCC tissues analyzed, 21 (67.7%) exhibited an overexpression of cyclin E protein. In contrast to cyclin E gene expression, cyclin D1 expression was strongly downregulated in 19 (61.2%) HCCs. Interestingly, 65% of HCC tissues with overexpression of the cyclin E gene exhibited downregulation of cyclin D1, suggesting reciprocal deregulation of these cyclins in the G1 progression of the cell cycle. Southern blot analysis proved the amplification of cyclin E gene in HCC with a high level of overexpression. The present findings suggest that the reciprocal deregulation of cyclin E lacking cyclin D1 expression might play a role in G1 progression and the development of HCC.
Keywords :
Hepatocellular carcinoma , Cyclin E , Cyclin D1 , Reciprocal expression