Sagara N, Katoh M
Genetics and Cell Biology Section, Genetics Division, National Cancer Center Research Institute, Tokyo, Japan.
Cancer Res. 2000 Nov 1;60(21):5959-62.
TCF transcription factors are mediators of the WNT signaling pathway and are antagonized by the transforming growth factor beta signaling pathway. Here human TCF-3 has been cloned and characterized. Differential expression analyses of TCF genes in gastric cancer revealed that TCF-1 was expressed in most cases of primary gastric cancer at almost the same level as in normal gastric mucosa and that TCF-3 was occasionally up-regulated in primary gastric cancer. The TCF-3 expression vector was transfected to gastric cancer cell line MKN28 to establish stable transformants. Three independent MKN28 transformants overexpressing TCF-3 showed about 8-fold resistance to mitomycin C (MMC; IC50, 2.4 microg/ml) compared with MKN28 vector transfectants (IC50 = 0.3 microg/ml). Among the 10 drug resistance-associated genes examined in this study, the DT-diaphorase (DTD) gene was down-regulated in three MKN28 transformants overexpressing TCF-3. DTD mRNA was also down-regulated in primary gastric cancer with TCF-3 up-regulation. In addition, DTD protein was down-regulated in three MKN28 transformants overexpressing TCF-3 compared with MKN28 vector transfectants. DTD is implicated in the activation of MMC in target cells, and DTD down-regulation explains MMC resistance. MMC resistance induced by TCF-3 overexpression is probably due to DTD down-regulation, which might provide a possible target for new therapy of drug-resistant gastric cancer.
TCF转录因子是WNT信号通路的介质,并受到转化生长因子β信号通路的拮抗。在此,已克隆并鉴定了人TCF-3。胃癌中TCF基因的差异表达分析显示,大多数原发性胃癌病例中TCF-1的表达水平与正常胃黏膜几乎相同,而原发性胃癌中TCF-3偶尔会上调。将TCF-3表达载体转染至胃癌细胞系MKN28以建立稳定的转化体。与MKN28载体转染体(IC50 = 0.3μg/ml)相比,三个过表达TCF-3的独立MKN28转化体对丝裂霉素C(MMC;IC50,2.4μg/ml)表现出约8倍的抗性。在本研究中检测的10个耐药相关基因中,DT-黄递酶(DTD)基因在三个过表达TCF-3的MKN28转化体中下调。在TCF-3上调的原发性胃癌中,DTD mRNA也下调。此外,与MKN28载体转染体相比,三个过表达TCF-3的MKN28转化体中DTD蛋白下调。DTD参与靶细胞中MMC的激活,DTD下调解释了MMC耐药性。TCF-3过表达诱导的MMC耐药性可能是由于DTD下调,这可能为耐药性胃癌的新治疗提供一个可能的靶点。