Diaz-Guerra M, Haddow S, Bauluz C, Jorcano J L, Cano A, Balmain A, Quintanilla M
Dept. Bioquimica Facultad de Medicina UAM, Madrid, Spain.
Cancer Res. 1992 Feb 1;52(3):680-7.
Activation of a Harvey ras (H-ras) protooncogene is a frequent event associated with mouse epidermal carcinogenesis. We report that the transfection of a human H-ras oncogene into an immortalized mouse epidermal cell line (MCA3D) induces the anomalous expression of cytokeratins (CKs) 8 and 18 characteristic of simple epithelia. The comparison of various transfectant cell clones indicated a direct correlation between the levels of CK8 expression and the mutated H-ras p21s. The expression of simple epithelial CKs is also described in cell lines derived from mouse skin carcinomas (HaCa4, CarC) and in keratinocytes transformed in vitro by a chemical carcinogen (PDV, PDVC57), all of which contain altered H-ras genes. The induction of CK8 and CK18 occurs at the mRNA level and, although both CK8 and CK18 mRNAs are expressed, CK18 protein does not accumulate whereas CK8 is incorporated into intermediate filaments. Immunofluorescence studies show that the pattern of CK8 protein expression is heterogeneous; some cells express very low amounts of CK8, whereas others synthesize relatively high levels of this protein. However, selection of strongly CK8-positive cells was found in one case where a more malignant population of cells (PDVC57) was derived by tumor transplantation of PDV. Our results suggest that activation of a H-ras gene can alter the normal differentiation program of epidermal cells and that the ability to synthesize CK8 and CK18 could be related to tumor progression.
哈维鼠肉瘤病毒癌基因(H-ras)的激活是与小鼠表皮癌发生相关的常见事件。我们报道,将人H-ras癌基因转染到永生化小鼠表皮细胞系(MCA3D)中可诱导简单上皮细胞特征性的细胞角蛋白(CKs)8和18异常表达。对各种转染细胞克隆的比较表明,CK8表达水平与突变的H-ras p21之间存在直接相关性。在源自小鼠皮肤癌的细胞系(HaCa4、CarC)以及经化学致癌物体外转化的角质形成细胞(PDV、PDVC57)中也描述了简单上皮CKs的表达,所有这些细胞系都含有改变的H-ras基因。CK8和CK18的诱导发生在mRNA水平,并且尽管CK8和CK18 mRNA均表达,但CK18蛋白不积累,而CK8则被整合到中间丝中。免疫荧光研究表明,CK8蛋白的表达模式是异质性的;一些细胞表达的CK8量非常低,而另一些细胞合成的这种蛋白水平相对较高。然而,在一例通过PDV肿瘤移植获得更具恶性的细胞群体(PDVC57)的情况中,发现了强CK8阳性细胞的选择。我们的结果表明,H-ras基因的激活可改变表皮细胞的正常分化程序,并且合成CK8和CK18的能力可能与肿瘤进展有关。