Ng I O, Liang Z D, Cao L, Lee T K
Department of Pathology, University of Hong Kong, Queen Mary Hospital, China.
Cancer Res. 2000 Dec 1;60(23):6581-4.
We investigated the expression and deletion of DLC-1 (frequently deleted in liver cancer gene), first reported in 1998 and having a high homology with rat p122RhoGAP in hepatocellular carcinoma (HCC). Six (20%) of 30 human HCC samples and 2 (40%) of 5 HCC cell lines were found to have no detectable DLC-1 expression by reverse transcription-PCR. Homozygous DLC-1 deletion was detected by Southern blotting in two of six HCC samples and in both HCC cell lines with no DLC-1 expression. Transfection of DLC-1 into 5 HCC cell lines (two with DLC-1 deletion and three with intact DLC-1) showed significant growth inhibition in these two HCC cell lines with deleted DLC-1 with both 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide and colony formation assays but not in three other HCC cell lines with intact DLC-1. Our findings suggest that DLC-1 may play an important role in hepatocarcinogenesis.
我们研究了肝癌缺失基因1(DLC-1,1998年首次报道,与大鼠p122RhoGAP在肝细胞癌(HCC)中具有高度同源性)的表达和缺失情况。通过逆转录聚合酶链反应(RT-PCR)发现,30例人类肝癌样本中有6例(20%)以及5种肝癌细胞系中有2例(40%)未检测到DLC-1表达。通过Southern印迹法在6例肝癌样本中的2例以及2种无DLC-1表达的肝癌细胞系中检测到了DLC-1纯合缺失。将DLC-1转染到5种肝癌细胞系(2种有DLC-1缺失,3种有完整的DLC-1)中,通过3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)法和集落形成试验发现,在这2种有DLC-1缺失的肝癌细胞系中出现了显著的生长抑制,而在另外3种有完整DLC-1的肝癌细胞系中则未出现。我们的研究结果表明,DLC-1可能在肝癌发生过程中起重要作用。