Khokha R, Waterhouse P, Yagel S, Lala P K, Overall C M, Norton G, Denhardt D T
Department of Biochemistry, University of Western Ontario, London, Canada.
Science. 1989 Feb 17;243(4893):947-50. doi: 10.1126/science.2465572.
Mouse 3T3 cell lines capable of constitutively synthesizing an RNA complementary to the messenger RNA encoding TIMP, tissue inhibitor of metalloproteinases, were constructed by transfection with appropriate plasmid constructs. Many of the lines were down-modulated for TIMP messenger RNA levels and secreted less TIMP into the culture medium. In comparison to noninvasive, nontumorigenic controls, these cells not only were invasive in a human amnion invasion assay, but also were tumorigenic and metastatic in athymic mice. These results indicate that TIMP suppresses oncogenicity, at least in immortal murine 3T3 cells.
通过用合适的质粒构建体转染,构建了能够组成性合成与编码金属蛋白酶组织抑制剂(TIMP)的信使核糖核酸互补的核糖核酸的小鼠3T3细胞系。许多细胞系中TIMP信使核糖核酸水平下调,并且向培养基中分泌的TIMP减少。与非侵袭性、非致瘤性对照相比,这些细胞不仅在人羊膜侵袭试验中具有侵袭性,而且在无胸腺小鼠中具有致瘤性和转移性。这些结果表明,TIMP至少在永生化的小鼠3T3细胞中抑制致癌性。