作者: Dai Yuedi , Cai Yuankun , Zhao Jiaying , Liu Han , Wang Yueqi
DOI: 10.18632/ONCOTARGET.19741
关键词:
摘要: Aberrant activation of beta-catenin/TCF (T-cell factor) signaling is frequently observed in the pancreatic cancer. However, regulation nuclear transcription machinery remains largely unknown. In this study, TFCP2 (transcriptional factor CP2) expression cancer was detected by qPCR, immunohistochemistry and western blot. Western blot, colony formation assay, migration invasion experiment were performed to investigate effects on growth cells. vivo, mouse metastasis models utilized determine ability. blots used evaluate related protein expression. Luciferase reporter assay explore role signaling. We have shown that up-regulated Over-expression promoted growth, migration, cells, while knocking down inhibited invasion, The mechanism study revealed interacted beta-catenin, enhanced interaction between beta-catenin TCF4, activated Taken together, our demonstrated oncogenic roles cancer, suggested might be a target for treatment