Kubota S, Kiyosawa H, Nomura Y, Yamada T, Seyama Y
Department of Physiological Chemistry and Nutrition, Faculty of Medicine, The University of Tokyo, Bunkyo-ku, Japan.
J Natl Cancer Inst. 1997 Apr 16;89(8):567-71. doi: 10.1093/jnci/89.8.567.
Ornithine decarboxylase (ODC) plays a pivotal role in the synthesis of polyamines, a group of chemical compounds that are essential for cell growth. Recent reports have shown that ODC overexpression may be involved in malignant transformation of immortalized NIH 3T3 cells. We have demonstrated that ODC-overproducing mouse breast cancer cells are more invasive in vitro than control cells. However, little information is available concerning the relationship between ODC overexpression, tumor invasion, and metastasis and the signal transduction pathways involved in ODC-induced transformation and invasion.
Our purpose was twofold: 1) to determine whether ODC overexpression is directly involved in tumor cell invasion and 2) to determine whether ODC overexpression induces mitogen-activated protein (MAP) kinase activities that are associated with cell growth and transformation.
We transfected C3H clone 8 mouse 10T1/2 fibroblasts with an expression vector that carries a complementary DNA encoding rat ODC. Neomycin-resistant cells that overproduced ODC (4-6.5 times the control levels) were isolated. The transformed phenotype of these cells was determined by assessing colony formation and anchorage-independent growth in soft agar. The invasiveness of the cells was studied by means of an invasion assay that used Matrigel-coated filters in Boyden chambers. The MAP kinase activity of the cells was assayed by an in-gel kinase assay, using myelin basic protein as the substrate.
Overexpression of ODC induced not only cell transformation and anchorage-independent growth in soft agar but also invasiveness through a Matrigel-coated filter. The ODC-overproducing transfectants showed enhanced MAP kinase activity that paralleled the magnitude of cell invasiveness.
ODC plays a pivotal role not only in cell transformation but also in cancer cell invasion. ODC overexpression enhanced MAP kinase activity.
Our results demonstrate a connection between the polyamine/ODC and the MAP kinase signal transduction pathways and suggest that MAP kinase may play a pivotal role in ODC-induced cell transformation and invasion.
鸟氨酸脱羧酶(ODC)在多胺合成中起关键作用,多胺是一组对细胞生长至关重要的化合物。最近的报告表明,ODC过表达可能参与永生化NIH 3T3细胞的恶性转化。我们已经证明,过量产生ODC的小鼠乳腺癌细胞在体外比对照细胞更具侵袭性。然而,关于ODC过表达、肿瘤侵袭和转移之间的关系以及ODC诱导的转化和侵袭所涉及的信号转导途径,目前所知甚少。
我们的目的有两个:1)确定ODC过表达是否直接参与肿瘤细胞侵袭;2)确定ODC过表达是否诱导与细胞生长和转化相关的丝裂原活化蛋白(MAP)激酶活性。
我们用携带编码大鼠ODC互补DNA的表达载体转染C3H克隆8小鼠10T1/2成纤维细胞。分离出过量产生ODC(是对照水平的4 - 6.5倍)的新霉素抗性细胞。通过评估集落形成和在软琼脂中不依赖贴壁生长来确定这些细胞的转化表型。通过在Boyden小室中使用基质胶包被的滤膜的侵袭试验来研究细胞的侵袭性。使用髓鞘碱性蛋白作为底物,通过凝胶内激酶试验测定细胞的MAP激酶活性。
ODC的过表达不仅诱导细胞转化和在软琼脂中不依赖贴壁生长,还诱导通过基质胶包被滤膜的侵袭性。过量产生ODC的转染子显示出增强的MAP激酶活性,这与细胞侵袭程度平行。
ODC不仅在细胞转化中起关键作用,而且在癌细胞侵袭中也起关键作用。ODC过表达增强了MAP激酶活性。
我们的结果证明了多胺/ODC和MAP激酶信号转导途径之间的联系,并表明MAP激酶可能在ODC诱导的细胞转化和侵袭中起关键作用。