Ishikawa S, Egami H, Kurizaki T, Akagi J, Tamori Y, Yoshida N, Tan X, Hayashi N, Ogawa M
Dept. of Surgery II, Kumamoto University Medical School, Kumamoto, Japan.
J Exp Clin Cancer Res. 2003 Jun;22(2):299-306.
The difference in gene expression between the highly invasive and metastatic cell line PC-1.0 and the weakly invasive and metastatic cell line PC-1 both derived from a pancreatic ductal carcinoma induced by N-nitrosobis (2-oxopropyl) amine (BOP) in Syrian golden hamster was examined using the Representational Difference Analysis (RDA) method. Within 8 clones (cDNA fragments) successfully isolated after subtraction hybridization of PC-1 cDNA from PC-1.0, 5 clones were shown to be specific or highly expressed in PC-1.0 as confirmed by RT-PCR. Among these 5 clones, two known genes, MAP kinase kinase 2 (MKK2) and phosphatidylinositol 4-kinase (PI4K230) were detected by gene sequencing. The specific expressions of MKK2 and PI4K230 in the highly invasive and metastatic cell line PC-1.0 were confirmed by RT-PCR and Northern blotting. By adding the CM of PC1.0 which included the cancer cell dissociation factor (DF), PC-1 cells began to dissociate and migrate from the colonies, and in addition the expression of MKK2 was found to be induced. On the other hand, the expression of PI4K230 was not induced in PC-1 cells by adding the CM of PC-1.0. Interestingly, in PC-1.0 the expression of PI4K230 was completely abolished and apoptosis induced by the PI3K inhibitor wortmannin. These results suggest that both MKK2 and PI4K230 are factors of a signal transduction pathway that might play an important role related to invasion and metastasis through the induction of cell motility and/or the inhibition of apoptosis.
利用代表性差异分析(RDA)方法,研究了源自叙利亚金仓鼠经N-亚硝基双(2-氧代丙基)胺(BOP)诱导的胰腺导管癌的高侵袭性和转移性细胞系PC-1.0与低侵袭性和转移性细胞系PC-1之间的基因表达差异。在从PC-1.0中减去PC-1的cDNA进行消减杂交后成功分离出的8个克隆(cDNA片段)中,经逆转录聚合酶链反应(RT-PCR)证实,有5个克隆在PC-1.0中特异性表达或高表达。在这5个克隆中,通过基因测序检测到两个已知基因,即丝裂原活化蛋白激酶激酶2(MKK2)和磷脂酰肌醇4-激酶(PI4K230)。通过RT-PCR和Northern印迹法证实了MKK2和PI4K230在高侵袭性和转移性细胞系PC-1.0中的特异性表达。通过添加包含癌细胞解离因子(DF)的PC1.0的条件培养基(CM),PC-1细胞开始从集落中解离并迁移,此外还发现MKK2的表达被诱导。另一方面,添加PC-1.0的CM并未诱导PC-1细胞中PI4K230的表达。有趣的是,在PC-1.0中,PI4K230的表达完全被消除,并且磷脂酰肌醇3-激酶(PI3K)抑制剂渥曼青霉素诱导了细胞凋亡。这些结果表明MKK2和PI4K230都是信号转导途径的因子,可能通过诱导细胞运动和/或抑制细胞凋亡在侵袭和转移中发挥重要作用。