4.7 Article

The inhibition of pancreatic cancer invasion-metastasis cascade in both cellular signal and blood coagulation cascade of tissue factor by its neutralisation antibody

Journal

EUROPEAN JOURNAL OF CANCER
Volume 47, Issue 14, Pages 2230-2239

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.ejca.2011.04.028

Keywords

Pancreatic cancer; Tissue factor; Metastasis; Blood coagulation; Matrix metalloproteinase 9

Categories

Funding

  1. Ministry of Health, Labor and Welfare (Matsumura) [H19-025]
  2. Ministry of Education, Culture, Sports, Science and Technology (Matsumura) [17016087]
  3. Japanese Foundation for Multidisciplinary Treatment of Cancer (Matsumura)
  4. Funding Program for World-Leading Innovative R&D on Science and Technology (FIRST Program)
  5. Princess Takamatsu Cancer Research Fund [07-23908]
  6. Japan Society for the Promotion of Science
  7. Grants-in-Aid for Scientific Research [17016087] Funding Source: KAKEN

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Tissue factor (TF), the initiating cell surface receptor for the blood coagulation cascade, plays an important role in malignant transformation of the pancreas, although the precise mechanism remains unresolved. Here, we report that the TF - factor Vila complex in human pancreatic cancer cells produced a significant amount of MMP-9 and promoted invasion ability in vitro and invasion and metastasis in vivo. For treatment, we successfully developed an anti-human TF monoclonal antibody that inhibits both cellular signalling and blood coagulation cascade via TF. Invasive capability and MMP-9 expression were significantly reduced by the antibody. The antibody inhibited not only tumour invasion in the orthotopic model, but also haematogenous metastasis in the portal-injection liver metastasis model. In conclusion, the TF-VIIa complex plays an important role in invasion-metastasis by enhancing tumour cell infiltration ability and forming microthrombi. The newly established anti-human TF neutralisation antibody may be useful for the treatment of pancreatic and other invasive cancers. (C) 2011 Elsevier Ltd. All rights reserved.

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