Metformin Inhibits Tumor Metastasis through Suppressing Hsp90? Secretion in an AMPK?1-PKC? Dependent Manner.
Ontology highlight
ABSTRACT: Metformin has been documented in epidemiological studies to mitigate tumor progression. Previous reports show that metformin inhibits tumor migration in several cell lines, such as MCF-7 and H1299, but the mechanisms whereby metformin exerts its inhibitory effects on tumor metastasis remain largely unknown. The secreted proteins in cancer cell-derived secretome have been reported to play important roles in tumor metastasis, but whether metformin has an effect on tumor secretome remains unclear. Here we show that metformin inhibits tumor metastasis by suppressing Hsp90? (heat shock protein 90?) secretion. Mass spectrometry (MS) analysis and functional validation identify that eHsp90? (extracellular Hsp90?) is one of the most important secreted proteins for metformin to inhibit tumor cells migration, invasion and metastasis both in vitro and in vivo. Moreover, we find that metformin inhibits Hsp90? secretion in an AMPK?1 dependent manner. Our data elucidate that AMPK?1 (AMP-activated protein kinase ?1) decreases the phosphorylation level of Hsp90? by inhibiting the kinase activity of PKC? (protein kinase C?), which suppresses the membrane translocation and secretion of Hsp90?. Collectively, our results illuminate that metformin inhibits tumor metastasis by suppressing Hsp90? secretion in an AMPK?1 dependent manner.
SUBMITTER: Gong Y
PROVIDER: S-EPMC7016760 | biostudies-literature | 2020 Jan
REPOSITORIES: biostudies-literature
ACCESS DATA