| Literature DB >> 31082618 |
Gastón Amable1, Eduardo Martínez-León1, María Elisa Picco1, Nicolas Di Siervi2, Carlos Davio3, Enrique Rozengurt4, Osvaldo Rey5.
Abstract
Several epidemiologic studies have revealed strong inverse associations between metformin use and risk of colorectal cancer development. Nevertheless, the underlying mechanisms are still uncertain. The Wnt/β-catenin pathway, which plays a central role in intestinal homeostasis and sporadic colorectal cancer development, is regulated by phosphorylation cascades that are dependent and independent of Wnt. Here we report that a non-canonical Ser552 phosphorylation in β-catenin, which promotes its nuclear accumulation and transcriptional activity, is blocked by metformin via AMPK-mediated PI3K/Akt signaling inhibition.Entities:
Keywords: AMPK; Colorectal cancer; Metformin; PI3K/Akt; β-Catenin
Mesh:
Substances:
Year: 2019 PMID: 31082618 DOI: 10.1016/j.biocel.2019.05.004
Source DB: PubMed Journal: Int J Biochem Cell Biol ISSN: 1357-2725 Impact factor: 5.085