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Antibody-based targeting of alternatively spliced tissue factor: A new approach to impede the primary growth and spread of pancreatic ductal adenocarcinoma

  • Dusten Unruh
  • , Betü Ünlü
  • , Clayton S. Lewis
  • , Xiaoyang Qi
  • , Zhengtao Chu
  • , Robert Sturm
  • , Ryan Keil
  • , Syed A. Ahmad
  • , Timofey Sovershaev
  • , Mariette Adam
  • , Patrick Van Dreden
  • , Barry J. Woodhams
  • , Divya Ramchandani
  • , Georg F. Weber
  • , Janusz W. Rak
  • , Alisa S. Wolberg
  • , Nigel Mackman
  • , Henri H. Versteeg
  • , Vladimir Y. Bogdanov

Research output: Contribution to journalArticlepeer-review

22 Scopus citations

Abstract

Alternatively spliced Tissue Factor (asTF) is a secreted form of Tissue Factor (TF), the trigger of blood coagulation whose expression levels are heightened in several forms of solid cancer, including pancreatic ductal adenocarcinoma (PDAC). asTF binds to β1 integrins on PDAC cells, whereby it promotes tumor growth, metastatic spread, and monocyte recruitment to the stroma. In this study, we determined if targeting asTF in PDAC would significantly impact tumor progression. We here report that a novel inhibitory anti-asTF monoclonal antibody curtails experimental PDAC progression. Moreover, we show that tumor-derived asTF is able to promote PDAC primary growth and spread during early as well as later stages of the disease. This raises the likelihood that asTF may comprise a viable target in early- and late-stage PDAC. In addition we show that TF expressed by host cells plays a significant role in PDAC spread. Together, our data demonstrate that targeting asTF in PDAC is a novel strategy to stem PDAC progression and spread.

Original languageEnglish
Pages (from-to)25264-25275
Number of pages12
JournalOncotarget
Volume7
Issue number18
DOIs
StatePublished - 1 May 2016
Externally publishedYes

Keywords

  • Alternative splicing
  • Metastasis
  • Pancreatic cancer
  • Tissue factor
  • β1 integrins

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