Xin L W, Martinerie C, Zumkeller W, Westphal M, Perbal B
Laboratoire d'Oncologie Virale et Moléculaire, Institut Curie-Recherche, 91405 Orsay Cedex, France.
Clin Mol Pathol. 1996 Apr;49(2):M91-7. doi: 10.1136/mp.49.2.m91.
Aims-(1) To investigate the expression in human derived glioblastoma cell lines of two structurally related genes, novH (nephroblastoma overexpressed gene) and CTGF (connective tissue growth factor), which encode putative insulin-like growth factor binding proteins of a novel type. (2) To investigate whether the same transcription factors regulate CTGF and novH expression.Methods-Expression of novH and CTGF was analysed in 24 glioblastoma derived cell lines by northern blotting. The CTGF promoter region was characterised by nucleotide sequencing, RNase protection experiments, by transient transfections, and CAT assays.Results-CTGF and novH mRNA levels differed in the glioma cell lines studied. NovH and CTGF genes were not co-expressed in all cell lines. The CTGF promoter region was highly conserved compared with the corresponding region in the mouse (FISP12) and exhibited in vitro transcriptional activity.Conclusions-Although the coding regions of novH and CTGF are highly homologous, their promoter regions are substantially different, suggesting that these two genes may be regulated by different mechanisms. Considering that novH and CTGF are likely to be, respectively, negative and positive regulators of growth and that some glioma cell lines expressing novH are not tumorigenic, expression of these two genes might represent a key element in determining the stage of differentiation or the malignant potential, or both, of some tumour cell lines.
目的——(1)研究两种结构相关基因novH(肾母细胞瘤过度表达基因)和CTGF(结缔组织生长因子)在人源胶质母细胞瘤细胞系中的表达,这两种基因编码一种新型的假定胰岛素样生长因子结合蛋白。(2)研究是否相同的转录因子调节CTGF和novH的表达。
方法——通过Northern印迹分析24种胶质母细胞瘤衍生细胞系中novH和CTGF的表达。通过核苷酸测序、RNA酶保护实验、瞬时转染和CAT分析对CTGF启动子区域进行表征。
结果——在所研究的胶质瘤细胞系中,CTGF和novH mRNA水平有所不同。NovH和CTGF基因并非在所有细胞系中都共表达。与小鼠相应区域(FISP12)相比,CTGF启动子区域高度保守,并表现出体外转录活性。
结论——尽管novH和CTGF的编码区高度同源,但其启动子区域存在显著差异,表明这两个基因可能受不同机制调控。鉴于novH和CTGF可能分别是生长的负性和正性调节因子,且一些表达novH的胶质瘤细胞系不具有致瘤性,这两个基因的表达可能是决定某些肿瘤细胞系分化阶段或恶性潜能,或两者的关键因素。