In this study, we aimed to investigate the role of miRNA-429 in the pathogenesis of pancreatic ductal
adenocarcinoma(PDAC) and the potential mechanism of this procedure. Totally 95 consecutive patients with PDAC diagnosed by pathology were retrospectively collected from June 1st , 2015 to August 30th, 2019 in Department of General Surgery, Jingmen First People's Hospital. The human
pancreatic cancer cell line Bxpc-3 and Panc-1 were used and the cell proliferation and migration were detected by MTT assays and Transwell assays, respectively. The quantitative real-time polymerase chain reaction (qRT-PCR) was applied to evaluate the expression in
RNA level. Our results showed that overexpression of miRNA-429 could suppress the cell invasion, proliferation and
metastasis through regulating the process of EMT in PDAC cell line, while low expression of miRNA-429 had the opposite effects. We demonstrated that miRNA-429 had critical roles in the pathogenesis of PDAC. Clinically, we observed that
tumor tissues from patients with PDAC exhibited significantly decreasing in miRNA-429 expression compared with the non-
tumor tissues. Additionally, decreased expression of miRNA-429 in
tumor tissues of patients with PDAC was associated with poorer prognosis and several clinical-pathological characteristics. In conclusion, miRNA-429 exerted anti-
tumor functions in PDAC through the regulation of EMT process. The results of this study would provide a novel insight into
tumorigenesis and the basis for the development of
miRNA-targeting
therapies against PDAC.