Transformation of rat bladder epithelial cells by introduction of a single oncogene.

Oncogene research Pub Date : 1991-01-01
A M Mann, M Stevenson, T Masui, C D Borgeson, S M Cohen
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Abstract

Malignant transformation of cells in vitro requires the action of cooperating oncogenes. However, the action of a single activated oncogene, if placed under a strong constitutive promoter, is sufficient to transform in vitro established cells. We have investigated the role of cooperating oncogenes in the transformation of normal rat bladder epithelial cells. Effects of polyoma middle T, v-Ha-ras or activated rat c-Ha-ras, independently or in combination with v-myc on in vitro and in vivo behavior of rat bladder epithelial cells were studied. Introduction of polyoma middle T alone, c-Ha-ras or in some cases v-myc into "normal" rat bladder epithelial cells was sufficient for full malignant transformation of these cells. In addition, introduction of polyoma middle T, activated c-Ha-ras or v-myc transformed cells into nude mice, resulted in development of highly invasive adenocarcinomas. These results indicate that full malignant transformation of normal rat bladder epithelial cells did not require the action of introduced cooperating oncogenes.

引入单一致癌基因对大鼠膀胱上皮细胞的转化作用。
细胞在体外的恶性转化需要协同癌基因的作用。然而,单个激活的癌基因的作用,如果置于强组成启动子下,就足以在体外建立的细胞中转化。我们研究了协同癌基因在正常大鼠膀胱上皮细胞转化中的作用。研究了多瘤中间T、v-Ha-ras或活化大鼠c-Ha-ras单独或与v-myc联合对大鼠膀胱上皮细胞体外和体内行为的影响。在“正常”大鼠膀胱上皮细胞中单独引入多瘤中间T、c-Ha-ras或在某些情况下引入v-myc,足以使这些细胞完全恶性转化。此外,将多瘤中间T、活化的c-Ha-ras或v-myc转化细胞导入裸鼠,导致高侵袭性腺癌的发展。这些结果表明,正常大鼠膀胱上皮细胞的完全恶性转化不需要引入协同癌基因的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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