Chen S C, Redenius D, Schwartz R C
Department of Microbiology, Michigan State University, East Lansing 48824-1101.
Biochem Biophys Res Commun. 1991 Aug 15;178(3):1343-50. doi: 10.1016/0006-291x(91)91041-a.
Seven tumors independently derived from a v-Ha-ras-expressing pre-B cell line were examined to determine the oncogene activations cooperating with v-Ha-ras in in vivo tumor progression. The pre-B cell line was generated by infection with Moloney murine leukemia virus (MoMuLV) and a MoMuLV-derived recombinant expressing v-Ha-ras. Two of seven tumors possessed a MoMuLV integration immediately upstream and in reverse transcriptional orientation to c-myc. This correlated with a 3-fold increased level of c-myc mRNA. Two other tumors displayed elevated c-myc mRNA levels, although the mechanism of enhanced expression was unclear. Thus the tumor progression of a v-Ha-ras-expressing murine pre-B cell line selects for the activation of c-myc.
对七个独立源自表达v-Ha-ras的前B细胞系的肿瘤进行了检查,以确定在体内肿瘤进展过程中与v-Ha-ras协同作用的癌基因激活情况。该前B细胞系是通过用莫洛尼鼠白血病病毒(MoMuLV)和一个表达v-Ha-ras的MoMuLV衍生重组体感染而产生的。七个肿瘤中有两个在紧邻c-myc上游且转录方向相反的位置发生了MoMuLV整合。这与c-myc mRNA水平增加3倍相关。另外两个肿瘤显示c-myc mRNA水平升高,尽管其表达增强的机制尚不清楚。因此,表达v-Ha-ras的小鼠前B细胞系的肿瘤进展选择了c-myc的激活。