Kolb E
Wissenschaftsbereich Tierbiochemie, Karl-Marx-Universität Leipzig.
Z Gesamte Inn Med. 1987 Nov 1;42(21):597-603.
In each cytoblast of mammals about 30 protooncogenes are present which during the embryonic, the fetal and the postnatal development, respectively, in certain cell types may temporarily or permanently be used for the formation of certain proteins. A part of these proteins is of importance for the furthering of the division (DNA-replication) and the differentiation of the cells. According to the qualities in the proteins formed by protooncogenes the protein kinases, the GTP binding proteins and the DNA binding proteins are differentiated. Under the influence of carcinogens and of cocarcinogens several protooncogenes are changed in their structure and displaced, respectively, within certain chromosomes. Thus they are transduced into oncogenes and evoke an increased formation of transforming proteins which initiate a dysregulation of the transcription in the nucleus. Several aspects of the activation of protooncogenes, of the development of tumours as well as of the origination of tumours by recessive mutation are described.
在哺乳动物的每个成细胞中大约存在30种原癌基因,在胚胎、胎儿和出生后的发育过程中,这些原癌基因在某些细胞类型中可能会暂时或永久地用于某些蛋白质的形成。这些蛋白质中的一部分对于促进细胞分裂(DNA复制)和分化具有重要意义。根据原癌基因形成的蛋白质的性质,可区分出蛋白激酶、GTP结合蛋白和DNA结合蛋白。在致癌物和促癌物的影响下,某些原癌基因的结构会发生改变,并分别在某些染色体内移位。因此,它们被转导为癌基因,并引发转化蛋白形成增加,从而引发细胞核转录失调。本文描述了原癌基因激活、肿瘤发展以及隐性突变引发肿瘤的几个方面。