miR-589 promotes gastric cancer aggressiveness by a LIFR-PI3K/AKT-c-Jun regulatory feedback loop

• Published in: Journal of experimental & clinical cancer research Vol. 37; no. 1; pp. 152 - 11
• Main Authors: Zhang, Feifei, Li, Kaitao, Pan, Mingxin, Li, Weidong, Wu, Juan, Li, Mingyi, Zhao, Liang, Wang, Hui
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 16.07.2018; BioMed Central; BMC
• Subjects: Analysis; Animals; Breast cancer; Cell growth; Cell Line, Tumor; Cytokines; Development and progression; DNA methylation; Experiments; Feedback; Feedback loop; Female; Gastric cancer; Gene expression; Genetic aspects; Health aspects; Humans; Kinases; Laboratories; Leukemia; LIFR; Liver cancer; Male; Medical prognosis; Metastasis; Mice; Mice, Nude; MicroRNA; MicroRNAs; MicroRNAs - metabolism; miR-589; Neoplasm Metastasis; Phosphatidylinositol 3-Kinases - metabolism; Physiological aspects; Proteins; Proto-Oncogene Proteins c-akt - metabolism; Stomach cancer; Stomach Neoplasms - genetics; Stomach Neoplasms - pathology; Tumorigenesis; China; United States > US; Feedback loop; LIFR; miR-589; Metastasis; Gastric cancer
• ISSN: 1756-9966; 0392-9078; 1756-9966
• DOI: 10.1186/s13046-018-0821-4

As novel biomarkers for various cancers, microRNAs negatively regulate genes expression via promoting mRNA degradation and suppressing mRNA translation. miR-589 has been reported to be deregulated in several human cancer types. However, its biological role has not been functionally characterized in gastric cancer. Here, we aim to investigate the biological effect of miR-589 on gastric cancer and to reveal the possible mechanism. Real-time PCR was performed to evaluate the expression of miR-589 in 34 paired normal and stomach tumor specimens, as well as gastric cell lines. Functional assays, such as wound healing, transwell assays and in vivo assays, were used to detect the biological effect of miR-589 and LIFR. We determined the role of miR-589 in gastric cancer tumorigenesis in vivo using xenograft nude models. Dual-luciferase report assays and Chromatin immunoprecipitation (ChIP) assay were performed for target evaluation, and the relationships were confirmed by western blot assay. MiR-589 expression was significantly higher in tumor tissues and gastric cancer cells than those in matched normal tissues and gastric epithelial cells, respectively. Clinically, overexpression of miR-589 is associated with tumor metastasis, invasion and poor prognosis of GC patients. Gain- and loss-of function experiments showed that miR-589 promoted cell migration, metastasis and invasion in vitro and lung metastasis in vivo. Mechanistically, we found that miR-589 directly targeted LIFR to activate PI3K/AKT/c-Jun signaling. Meanwhile, c-Jun bound to the promoter region of miR-589 and activated its transcription. Thus miR-589 regulated its expression in a feedback loop that promoted cell migration, metastasis and invasion. Our study identified miR-589, as an oncogene, markedly induced cell metastasis and invasion via an atypical miR-589-LIFR-PI3K/AKT-c-Jun feedback loop, which suggested miR-589 as a potential biomarker and/or therapeutic target for the gastric cancer management.