LncRNA-PVT1 aggravates severe acute pancreatitis by promoting autophagy via the miR-30a-5p/Beclin-1 axis.

Severe acute pancreatitis (SAP) is a serious abdominal disease associated with increased morbidity and high mortality rates. The initial pancreatic injury and inflammatory response, which begins within acinar cells, play vital roles in promoting SAP severity. Previous studies have indicated that overactivated autophagy in acinar cells increases the risk of SAP. Autophagy is affected by various signaling pathways, partially through long noncoding RNA (lncRNA)-PVT1. However, few studies have focused on the effect of lncRNA on autophagy in pancreatitis. Our results demonstrate that sodium taurocholate (STC) induces abnormal activation of the autophagic response in pancreatic acinar cells in vitro and in vivo. The lncRNA-PVT1 level was significantly upregulated in this process and was capable of targeting the miR-30a-5p/Beclin-1-mediated autophagy signaling pathway. Additionally, STC-induced pancreatic acinar cells injury and autophagy activation were all abrogated with the downregulation of lncRNA-PVT1 by shRNAs in vitro. Furthermore, we confirmed that the lncRNA-PVT1/miR-30a-5p/Beclin-1 axis induces abnormal autophagy in the pancreas of SAP rats. Collectively, these results demonstrate that the lncRNA-PVT1/miR-30a-5p/Beclin-1 axis is a potential target for improving SAP, thus providing a foundation for further development of therapeutics in the future.