Abstract

BackgroundInteractions between cancer cells and surrounding cancer-associated fibroblasts (CAFs) play an important role in cancer progression. Invasive ductal carcinoma (IDC) of the pancreas is characterized by abundant fibrous connective tissue called desmoplasia. Podoplanin (PDPN) is a lymphatic vessel marker (D2-40), and expression of PDPN by stromal CAFs has been reported to be a prognostic indicator in various types of cancer.MethodsExpression of PDPN in pancreatic IDCs was assessed by immunohistochemical examination in 105 patients who underwent pancreatic resection. Primary CAFs were established from pancreatic cancer tissue obtained by surgery. Quantitative reverse transcription-polymerase chain reaction and flow cytometric analysis were performed to investigate PDPN expression in CAFs. We sorted CAFs according to PDPN expression, and analyzed the functional differences between PDPN+ CAFs and PDPN– CAFs using indirect co-culture with pancreatic cancer cell lines. We also investigated the culture conditions to regulate PDPN expression in CAFs.ResultsPDPN expression in stromal fibroblasts was associated with lymphatic vessel invasion (P = 0.0461), vascular invasion (P = 0.0101), tumor size ≥3 cm (P = 0.0038), histological grade (P = 0.0344), Union for International Cancer Control classification T stage (P = 0.029), and shorter survival time (P < 0.0001). Primary CAFs showed heterogeneous PDPN expression in vitro. Moreover, migration and invasion of pancreatic cancer cell lines (PANC-1 and SUIT-2) were associated with PDPN expression in CAFs (P < 0.01) and expression of CD10, matrix metalloproteinase (MMP) 2, and MMP3. In cultured CAFs, PDPN positivity changed over time under several conditions including co-culture with cancer cells, different culture media, and addition of growth factor.ConclusionsPDPN-expressing CAFs enhance the progression of pancreatic IDC, and a high ratio of PDPN-expressing CAFs is an independent predictor of poor outcome. Understanding the regulation of the tumor microenvironment is an important step towards developing new therapeutic strategies.

Highlights

  • Interactions between cancer cells and surrounding cancer-associated fibroblasts (CAFs) play an important role in cancer progression

  • We examined PDPN expression in invasive ductal carcinoma (IDC) of the human pancreas using immunohistochemical methods, and investigated the functional roles of PDPN-expressing CAFs established from pancreatic Invasive ductal carcinoma (IDC) by cell sorting

  • We found that PDPN+ and PDPN– CAFs had functional differences associated with their expression of CD10, MMP3, and MMP2

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Summary

Introduction

Interactions between cancer cells and surrounding cancer-associated fibroblasts (CAFs) play an important role in cancer progression. Podoplanin (PDPN) is a lymphatic vessel marker (D2-40), and expression of PDPN by stromal CAFs has been reported to be a prognostic indicator in various types of cancer. Improvements in the survival of pancreatic cancer patients have been minimal, and the 5-year survival rate remains low [1]. In 1998, pancreatic stellate cells (PSCs) were identified in the pancreas [7,8]. PSCs are located close to the acinar cells, and retain abundant vitamin Acontaining lipid droplets in their cytoplasm as a quiescent phenotype [9]. Activated PSCs produce abundant extracellular matrix (ECM), leading to cancer progression [9,11]. CAFs have gained attention as a potential therapeutic target [12,13]

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