Author: Pruitt, Hawley C.; Devine, Daniel J.; Samant, Rajeev S.
Title: Roles of N-Myc and STAT interactor in cancer: From initiation to dissemination Document date: 2016_3_11
ID: k3vjqumq_23
Snippet: In addition to Wnt signaling, NMI also influences other factors known to promote stemness. The SOX10 protein was Figure 3 . NMI inhibits cancer progression. NMI expression in epithelial cells inhibits the Wnt and TGFb signaling pathways. NMI also increases the expression of DKK1, the secreted inhibitor of the LRP 5/6 receptor in the Wnt pathway. In addition, NMI increases levels of active GSK3b, thereby targeting b-catenin for degradation. In par.....
Document: In addition to Wnt signaling, NMI also influences other factors known to promote stemness. The SOX10 protein was Figure 3 . NMI inhibits cancer progression. NMI expression in epithelial cells inhibits the Wnt and TGFb signaling pathways. NMI also increases the expression of DKK1, the secreted inhibitor of the LRP 5/6 receptor in the Wnt pathway. In addition, NMI increases levels of active GSK3b, thereby targeting b-catenin for degradation. In parallel, NMI also binds STAT5 to enhance expression of its target gene SMAD7, the inhibitory SMAD, and subsequently dampens TGFb signaling. In the absence of NMI, b-catenin accumulates in the cytoplasm and is translocated to the nucleus where it binds TCF/LEF transcription factors to enhance transcription of Wnt pathway target genes. Decreased expression of NMI leads to enhanced transcription of EMT master regulators SLUG and ZEB2 downstream of TGFb signaling. As a result, cells that have lost NMI undergo morphological changes and become more invasive and metastatic.
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