| First Author | Asahina K | Year | 2020 |
| Journal | Am J Physiol Gastrointest Liver Physiol | Volume | 318 |
| Issue | 2 | Pages | G265-G276 |
| PubMed ID | 31760766 | Mgi Jnum | J:290584 |
| Mgi Id | MGI:6444042 | Doi | 10.1152/ajpgi.00218.2019 |
| Citation | Asahina K, et al. (2020) Moderate alcohol intake promotes pancreatic ductal adenocarcinoma development in mice expressing oncogenic Kras. Am J Physiol Gastrointest Liver Physiol 318(2):G265-G276 |
| abstractText | Kras mutations are associated with pancreatic ductal adenocarcinoma (PDAC). Although tobacco smoking, pancreatitis, and obesity are known environmental risk factors for PDAC, the contribution of moderate alcohol intake to PDAC remains elusive. In the present study, we tested whether a combination of risk factors or moderate alcohol intake induces PDAC development in mice. Control Pdx1(Cre) and Pdx1(Cre);LSL-Kras(G12D) mutant mice were fed a Western alcohol diet containing high levels of cholesterol and saturated fat, 3.5% alcohol, and lipopolysaccharide for 5 mo. In addition, mice were treated with cerulein, for induction of pancreatitis, and nicotine every month. Treatment with all of these risk factors promoted development of advanced pancreatic neoplasia and PDAC in the Pdx1(Cre);LSL-Kras(G12D) mice but not in the control Pdx1(Cre) mice. Moderate alcohol intake or Western diet feeding also significantly promoted advanced neoplasia and PDAC development in Pdx1(Cre);LSL-Kras(G12D) mice compared with mice fed a regular chow. Alcohol, but not Western diet, increased tumor development in the liver in the Pdx1(Cre);LSL-Kras(G12D) mice, but its origin remained elusive due to leakiness of Pdx1(Cre) in hepatocytes. RNA-seq analysis revealed that alcohol feeding increases expression of markers for tumors (Epcam, Krt19, Prom1, Wt1, and Wwtr1), stroma (Dcn, Fn1, and Tnc), and cytokines (Tgfb1 and Tnf) and decreases expression of Fgf21 and Il6 in the pancreatic tumor tissues. Immunostaining showed heterogeneous expression of nephronectin, S100 calcium-binding protein A6, and vascular cell adhesion molecule 1 in pancreatic tumors surrounded by podoplanin-positive stromal cells. Our data indicate that moderate alcohol drinking is a risk factor for development of PDAC.NEW & NOTEWORTHY Heavy alcohol intake has been suspected to be a risk factor of pancreatic ductal adenocarcinoma (PDAC) in humans. However, the contribution of moderate alcohol intake to PDAC development remains elusive. In the present study, we experimentally show that moderate alcohol feeding significantly induces advanced stages of pancreatic intraepithelial neoplasia development and invasive PDAC in Pdx1(Cre);LSL-Kras(G12D) mutant mice. Our data indicate that moderate alcohol drinking is a risk factor for PDAC. |
