Ashida Shingo, Nishimori Isao, Tanimura Masanobu, Onishi Saburo, Shuin Taro
Department of Urology, Kochi Medical School, Nankoku, Kochi, Japan.
J Cancer Res Clin Oncol. 2002 Oct;128(10):561-8. doi: 10.1007/s00432-002-0374-x. Epub 2002 Aug 30.
Our primary goal was to determine whether increased expression of the transmembrane carbonic anhydrase (CA) isozymes in renal cell carcinoma (RCC) is regulated by the von Hippel-Lindau (VHL) gene.
We studied mRNA expression of all three transmembrane CAs - CA IX, XII, and XIV - in 17 RCC cell lines, transformants of the wild-type VHL gene, and normal kidney tissue cultures, and then compared them with the mutation status in the VHL gene.
Northern blot analysis showed no detectable signal for CA XIV mRNA expression in normal and cancer cells. CA XII mRNA was ubiquitously expressed except in two cell lines. Although CA XII expression levels tended to be lower in RCC cell lines without the VHL mutation and in transformants of the wild-type VHL gene, the results were not conclusive. Significant expression of CA IX mRNA was seen in eight of 17 RCC cell lines. Among five cell lines which had no VHL mutation, four lines showed no detectable signal and one cell line showed a low amount of CA IX mRNA expression. In patients with RCC, VHL mutations and significant CA IX expression were seen in established tumor cell lines but not in primary tissue cultures from normal counterparts. Further study of methylation status showed that the 5' region in the CA9 gene was hypomethylated in all CA IX-positive cell lines and hypermethylated in all CA IX-negative cell lines. Especially, methylation status at -74 and -6 CpG sites perfectly correlated with CA IX expression.
These findings indicate that VHL suppresses CA IX expression but has no conclusive effect on CA XII and XIV expressions in RCC. CA IX expression is also driven by the methylation status of the CA9 gene.
我们的主要目标是确定肾细胞癌(RCC)中跨膜碳酸酐酶(CA)同工酶的表达增加是否受冯·希佩尔-林道(VHL)基因调控。
我们研究了17种RCC细胞系、野生型VHL基因的转化体以及正常肾组织培养物中所有三种跨膜CA(CA IX、XII和XIV)的mRNA表达,然后将它们与VHL基因的突变状态进行比较。
Northern印迹分析显示正常细胞和癌细胞中未检测到CA XIV mRNA表达的信号。除两个细胞系外,CA XII mRNA普遍表达。虽然在无VHL突变的RCC细胞系和野生型VHL基因的转化体中,CA XII表达水平往往较低,但结果并不确凿。在17种RCC细胞系中的8种中观察到CA IX mRNA的显著表达。在5种无VHL突变的细胞系中,4种未检测到信号,1种细胞系显示低水平的CA IX mRNA表达。在RCC患者中,在已建立的肿瘤细胞系中观察到VHL突变和显著的CA IX表达,但在来自正常对应组织的原代组织培养物中未观察到。对甲基化状态的进一步研究表明,CA9基因的5'区域在所有CA IX阳性细胞系中低甲基化,在所有CA IX阴性细胞系中高甲基化。特别是,-74和-6 CpG位点的甲基化状态与CA IX表达完全相关。
这些发现表明,VHL抑制RCC中CA IX的表达,但对CA XII和XIV的表达没有确凿影响。CA IX的表达也受CA9基因甲基化状态的驱动。