MiR-143 and miR-145 inhibit gastric cancer cell migration and metastasis by suppressing MYO6.
Ontology highlight
ABSTRACT: Metastasis is a major clinical obstacle responsible for the high mortality and poor prognosis of gastric cancer (GC). MicroRNAs (miRNAs) are critical mediators of metastasis that act by modulating their target genes. In this study, we found that miR-143 and miR-145 act via a common target gene, MYO6, to regulate the epithelial-mesenchymal transition (EMT) and inhibit metastasis. We determined that miR-143 and miR-145 were downregulated in GC, and the ectopic expression of miR-143 and/or miR-145 inhibited GC cell migration and metastasis. Furthermore, MYO6 was identified as a direct common target of miR-143 and miR-145 and was elevated in GC. Silencing of MYO6 resulted in a metastasis-suppressive activity similar to that of miR-143 and miR-145, while restoring MYO6 attenuated the anti-metas
SUBMITTER: Lei C
PROVIDER: S-EPMC5682659 | biostudies-literature | 2017 Oct
REPOSITORIES: biostudies-literature
ACCESS DATA