Sejersen T, Jin P, Rahm M, Ringertz N R
Department of Medical Cell Genetics, Karolinska Institutet, Stockholm, Sweden.
Environ Health Perspect. 1989 Mar;80:247-56. doi: 10.1289/ehp.8980247.
Protooncogenes expressed in murine embryonal carcinoma (EC) cells or their differentiated daughter cells include more or less ubiquitously expressed protooncogenes such as c-myc, c-K-ras, and c-abl, as well as c-onc genes with a very restricted expression pattern. Examples of the latter are N-myc, c-mos, and int-2. These c-onc genes are transcriptionally active in EC cells, as well as in germ cells and/or early embryonic cells. When EC cells are induced to differentiate some protooncogenes or oncogene-related products undergo changes in expression. Thus, EC cell differentiation has been associated with increased expression of c-src, c-fos, int-1, int-2, and the epidermal growth factor (EGF) receptor, whereas decreased expression has been observed for c-mos, c-K-ras, c-myc, N-myc, and platelet-derived growth factor. The relationships between these changes in expression and EC cell differentiation are not understood. They may be important for the differentiation process or for expression of a differentiated phenotype. They may, however, also be secondary events with no functional significance to EC cell differentiation.
在小鼠胚胎癌细胞(EC)或其分化的子代细胞中表达的原癌基因包括或多或少普遍表达的原癌基因,如c-myc、c-K-ras和c-abl,以及表达模式非常受限的c-onc基因。后者的例子有N-myc、c-mos和int-2。这些c-onc基因在EC细胞以及生殖细胞和/或早期胚胎细胞中具有转录活性。当诱导EC细胞分化时,一些原癌基因或癌基因相关产物的表达会发生变化。因此,EC细胞分化与c-src、c-fos、int-1、int-2和表皮生长因子(EGF)受体的表达增加有关,而c-mos、c-K-ras、c-myc、N-myc和血小板衍生生长因子的表达则降低。这些表达变化与EC细胞分化之间的关系尚不清楚。它们可能对分化过程或分化表型的表达很重要。然而,它们也可能是对EC细胞分化没有功能意义的次要事件。