Deng X, Cao Y, Hu W, Gu H, Yao K
Cancer Research Institute, Hunan Medical University, Changsha.
Hunan Yi Ke Da Xue Xue Bao. 1997;22(2):102-4.
We have previously cloned a nasopharyngeal carcinoma transforming gene from human nasopharyngeal carcinoma cell line CNE-2 using mouse JB6 cell line as the recipient cells. This transforming gene, designated Tx, exhibits moderate transforming activity upon transfection into JB6 cells. Several lines of evidence indicate that the 2.8 kb EcoRI fragment which lies in the middle of the Tx gene is responsible for the transforming activity. The sequence of the 2.8 kb EcoRI fragment was determined, which showed striking homology with the human immunoglobulin light chain C region gene. Using the modified polymerase chain reaction-single strand conformation polymorphism analysis (PCR-SSCP) silver staining technique, we studied the possible point mutations of the nasopharyngeal carcinoma gene Tx in nasopharyngeal carcinoma. No mobility shift was detected in eleven paired cases of nasopharyngeal carcinoma biopsies suggesting that in most cases of nasopharyngeal carcinoma, the Tx gene is not activated via a mode of point mutation. Taken together with the previously obtained results we have found that the Tx gene is not activated by gene rearrangement or gene amplification. Therefore, we consider that the Tx gene may have been activated by its interaction with other regulatory factors.
我们先前利用小鼠JB6细胞系作为受体细胞,从人鼻咽癌细胞系CNE-2中克隆出一个鼻咽癌转化基因。这个被命名为Tx的转化基因,转染到JB6细胞后表现出中等程度的转化活性。多项证据表明,位于Tx基因中部的2.8 kb EcoRI片段负责转化活性。测定了该2.8 kb EcoRI片段的序列,发现其与人类免疫球蛋白轻链C区基因有显著同源性。我们采用改良的聚合酶链反应-单链构象多态性分析(PCR-SSCP)银染技术,研究了鼻咽癌基因Tx在鼻咽癌中的可能点突变。在11对鼻咽癌活检病例中未检测到迁移率改变,这表明在大多数鼻咽癌病例中,Tx基因不是通过点突变模式被激活的。结合先前获得的结果,我们发现Tx基因不是通过基因重排或基因扩增被激活的。因此,我们认为Tx基因可能是通过与其他调节因子相互作用而被激活的。