Lymphatic vessel remodeling and invasion in pancreatic cancer progression

Chia Ning Shen, King Siang Goh, Chi Ruei Huang, Tsai Chen Chiang, Chih Yuan Lee, Yung Ming Jeng, Shih Jung Peng, Hung Jen Chien, Mei Hsin Chung, Ya Hsien Chou, Chi Che Hsieh, Subhash Kulkarni, Pankaj J. Pasricha, Yu Wen Tien, Shiue Cheng Tang

Research output: Contribution to journalArticlepeer-review

33 Citations (Scopus)

Abstract

Background: The lymphatic system is involved in metastasis in pancreatic cancer progression. In cancer staging, lymphatic spread has been used to assess the invasiveness of tumor cells. However, from the endothelium's perspective, the analysis downplays the peri-lesional activities of lymphatic vessels. This unintended bias is largely due to the lack of 3-dimensional (3-D) tissue information to depict the lesion microstructure and vasculature in a global and integrated fashion. Methods: We targeted the pancreas as the model organ to investigate lymphatic vessel remodeling in cancer lesion progression. Transparent pancreases were prepared by tissue clearing to facilitate deep-tissue, tile-scanning microscopy for 3-D lymphatic network imaging. Findings: In human pancreatic ductal adenocarcinoma, we identify the close association between the pancreatic intraepithelial neoplasia (PanIN) lesions and the lymphatic network. In mouse models of PanIN (elastase-CreER;LSL-KrasG12D and elastase-CreER;LSL-KrasG12D;p53+/−), the 3-D image data reveal the peri-lesional lymphangiogenesis, endothelial invagination, formation of the bridge/valve-like luminal tubules, vasodilation, and luminal invasion. In the orthotopic mouse model of pancreatic cancer, we identify the localized, graft-induced lymphangiogenesis and the peri- and intra-tumoral lymphatic vessel invasion. Interpretation: The integrated view of duct lesions and vascular remodeling suggests an active role, rather than a passive target, of lymphatic vessels in the metastasis of pancreatic cancer. Our 3-D image data provide insights into the pancreatic cancer microenvironment and establish the technical and morphological foundation for systematic detection and 3-D analysis of lymphatic vessel invasion. Fund: Taiwan Academia Sinica (AS-107-TP-L15 and AS-105-TP-B15), Ministry of Science and Technology (MOST 106-2321-B-001-048, 106-0210-01-15-02, 106-2321-B-002-034, and 106-2314-B-007-004-MY2), and Taiwan National Health Research Institutes (NHRI EX107-10524EI).

Original languageEnglish
Pages (from-to)98-113
Number of pages16
JournalEBioMedicine
Volume47
DOIs
Publication statusPublished - Sept 2019
Externally publishedYes

Keywords

  • Cancer invasion
  • Kras mutation
  • Lymphangiogenesis
  • Lymphatic vessel
  • Lymphovascular invasion
  • Metastasis
  • p53 mutation
  • Pancreatic cancer
  • Pancreatic ductal adenocarcinoma
  • Pancreatic intraepithelial neoplasia

ASJC Scopus subject areas

  • General Biochemistry,Genetics and Molecular Biology

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