Caamano J, DiRado M, Iizasa T, Momiki S, Fernandes E, Ashendel C, Noda M, Klein-Szanto A J
Department of Pathology, Fox Chase Cancer Center, Philadelphia, Pennyslvania 19111.
Mol Carcinog. 1992;6(4):252-9. doi: 10.1002/mc.2940060406.
A human non-small-cell lung carcinoma cell line, Calu-6 (from an anaplastic carcinoma), was transfected with the Ki-ras-related anti-oncogene Krev-1. Several transfectant lines were obtained that showed a reduced tumorigenicity in nude mice with respect to the parental and control transfected cell lines. This decrease was approximately 50% in tumor incidence at 4 wk after subcutaneous inoculation of the transfected cells. In addition, the volume of the Calu-6 revertant-derived tumors was three to 10 times smaller than that of the equivalent tumors produced by inoculation of the control cell line transfected with the neomycin-resistance gene. Krev-1--transfected cells that exhibited reduced tumorigenicity expressed Krev-1 mRNA and had variable numbers of copies of the Krev-1 gene. Moreover, Krev-1--transfected cells exhibited a more differentiated squamous epithelial morphology than the parental and control cell lines did. Moderately elevated levels of protein kinase C activity were detected in some revertant clones. Such activity correlated with the level of expression of Krev-1 mRNA in most cases. In summary, Krev-1 induced important morphological and biological changes in transfected Calu-6 cells that we interpreted as partial reversion of the malignant phenotype.
用人非小细胞肺癌细胞系Calu-6(源自间变性癌)转染Ki-ras相关的抗癌基因Krev-1。获得了几个转染细胞系,相对于亲本细胞系和对照转染细胞系,这些转染细胞系在裸鼠中的致瘤性降低。在皮下接种转染细胞4周后,肿瘤发生率的降低约为50%。此外,Calu-6回复子衍生肿瘤的体积比接种新霉素抗性基因的对照细胞系产生的同等肿瘤小3至10倍。表现出致瘤性降低的Krev-1转染细胞表达Krev-1 mRNA,且Krev-1基因的拷贝数可变。此外,Krev-1转染细胞比亲本细胞系和对照细胞系表现出更分化的鳞状上皮形态。在一些回复子克隆中检测到蛋白激酶C活性适度升高。在大多数情况下,这种活性与Krev-1 mRNA的表达水平相关。总之,Krev-1在转染的Calu-6细胞中诱导了重要的形态和生物学变化,我们将其解释为恶性表型的部分逆转。