학술논문

Cadherin-11 Is a Cell Surface Marker Up-Regulated in Activated Pancreatic Stellate Cells and Is Involved in Pancreatic Cancer Cell Migration
Document Type
article
Source
American Journal Of Pathology. 187(1)
Subject
Biomedical and Clinical Sciences
Cancer
Pancreatic Cancer
Digestive Diseases
Rare Diseases
2.1 Biological and endogenous factors
Aetiology
Oral and gastrointestinal
Biomarkers
Tumor
Cadherins
Cell Line
Tumor
Cell Membrane
Cell Movement
Cell Proliferation
Gene Expression Regulation
Neoplastic
Gene Knockdown Techniques
Humans
Pancreas
Pancreatic Neoplasms
Pancreatic Stellate Cells
Up-Regulation
Medical and Health Sciences
Pathology
Biomedical and clinical sciences
Health sciences
Language
Abstract
Chronic pancreatitis is a prominent risk factor for the development of pancreatic ductal adenocarcinoma. In both conditions, the activation of myofibroblast-like pancreatic stellate cells (PSCs) plays a predominant role in the formation of desmoplastic reaction through the synthesis of connective tissue and extracellular matrix, inducing local pancreatic fibrosis and an inflammatory response. Yet the signaling events involved in chronic pancreatitis and pancreatic cancer progression and metastasis remain poorly defined. Cadherin-11 (Cad-11, also known as OB cadherin or CDH11) is a cell-to-cell adhesion molecule implicated in many biological functions, including tissue morphogenesis and architecture, extracellular matrix-mediated tissue remodeling, cytoskeletal organization, epithelial-to-mesenchymal transition, and cellular migration. In this study, we show that, in human chronic pancreatitis and pancreatic cancer tissues, Cad-11 expression was significantly increased in PSCs and pancreatic cancer cells. In particular, an increased expression of Cad-11 can be detected on the plasma membrane of activated PSCs isolated from chronic pancreatitis tissues and in pancreatic cancer cells metastasized to the liver. Moreover, knockdown of Cad-11 in cancer cells reduced pancreatic cancer cell migration. Taken together, our data underline the potential role of Cad-11 in PSC activation and pancreatic cancer metastasis.