IDEAS home Printed from https://ideas.repec.org/a/nat/nature/v434y2005i7031d10.1038_nature03357.html
   My bibliography  Save this article

The MET oncogene drives a genetic programme linking cancer to haemostasis

Author

Listed:
  • Carla Boccaccio

    (University of Turin Medical School)

  • Gabriella Sabatino

    (University of Turin Medical School)

  • Enzo Medico

    (University of Turin Medical School)

  • Flavia Girolami

    (University of Turin Medical School)

  • Antonia Follenzi

    (University of Turin Medical School)

  • Gigliola Reato

    (University of Turin Medical School)

  • Antonino Sottile

    (University of Turin Medical School)

  • Luigi Naldini

    (University of Turin Medical School)

  • Paolo M. Comoglio

    (University of Turin Medical School)

Abstract

Blood clotting and cancer Since migratory thrombophlebitis was noted by Trousseau during diagnosis of his own pancreatic cancer in 1865, blood clotting disorders have been regularly reported as a sign of occult (as in without readily detectable symptoms) malignancies. No direct link between tumorigenesis and blood clotting had been found, until now. In a mouse model for liver cancer, the human oncogene MET that triggers tumour development is shown to regulate genes responsible for haemostasis. Mice in which MET is active develop venous thromboses similar to those seen in human occult malignancies and overt cancers.

Suggested Citation

  • Carla Boccaccio & Gabriella Sabatino & Enzo Medico & Flavia Girolami & Antonia Follenzi & Gigliola Reato & Antonino Sottile & Luigi Naldini & Paolo M. Comoglio, 2005. "The MET oncogene drives a genetic programme linking cancer to haemostasis," Nature, Nature, vol. 434(7031), pages 396-400, March.
  • Handle: RePEc:nat:nature:v:434:y:2005:i:7031:d:10.1038_nature03357
    DOI: 10.1038/nature03357
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/nature03357
    File Function: Abstract
    Download Restriction: Access to the full text of the articles in this series is restricted.

    File URL: https://libkey.io/10.1038/nature03357?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    As the access to this document is restricted, you may want to search for a different version of it.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:nature:v:434:y:2005:i:7031:d:10.1038_nature03357. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.