IDEAS home Printed from https://ideas.repec.org/a/plo/pone00/0206007.html
   My bibliography  Save this article

The HER3 pathway as a potential target for inhibition in patients with biliary tract cancers

Author

Listed:
  • Angela Lamarca
  • Salvatore Galdy
  • Jorge Barriuso
  • Sharzad Moghadam
  • Elizabeth Beckett
  • Jane Rogan
  • Alison Backen
  • Catherine Billington
  • Mairéad G McNamara
  • Richard A Hubner
  • Angela Cramer
  • Juan W Valle

Abstract

Introduction: Expression of human epidermal growth factor receptor (HER)2 and HER3 have been investigated in small BTC studies using variable scoring systems. Methods: HER2 and HER3 overexpression/amplification were explored following internationally agreed guidelines using immunohistochemistry (IHC) and fluorescent in-situ hybridisation (FISH), respectively. Logistic regression and survival analysis (Kaplan Meier, Log rank test and Cox Regression) were used for statistical analysis. Results: Sixty-seven eligible patients with Stage I/II (31.3%) or III/IV (68.7%) disease at diagnosis were included. Membrane HER2 overexpression/amplification was identified in 1 patient (1%). HER3 overexpression was predominantly cytoplasmic; the rate of overexpression/amplification of HER3 in membrane and cytoplasm was 16% [ampullary cancer (AMP) (1/13; 8%), gallbladder cancer (GBC) (1/10; 10%), intra-hepatic cholangiocarcinoma (ICC) (6/26; 23%), extra-hepatic cholangiocarcinoma (ECC) (3/18; 17%)] and 24% [AMP (1/13; 8%), GBC (1/10; 10%), ICC (10/26; 38%), ECC (4/18; 22%)], respectively. Conclusions: A significant subset of patients with BTC expressed HER3. Inhibition of HER3 warrants further investigation. A better understanding of the downstream effects of HER3 in BTC requires further mechanistic investigations to identify new biomarkers and improve patient selection for future clinical trials.

Suggested Citation

  • Angela Lamarca & Salvatore Galdy & Jorge Barriuso & Sharzad Moghadam & Elizabeth Beckett & Jane Rogan & Alison Backen & Catherine Billington & Mairéad G McNamara & Richard A Hubner & Angela Cramer & J, 2018. "The HER3 pathway as a potential target for inhibition in patients with biliary tract cancers," PLOS ONE, Public Library of Science, vol. 13(10), pages 1-19, October.
  • Handle: RePEc:plo:pone00:0206007
    DOI: 10.1371/journal.pone.0206007
    as

    Download full text from publisher

    File URL: https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0206007
    Download Restriction: no

    File URL: https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0206007&type=printable
    Download Restriction: no

    File URL: https://libkey.io/10.1371/journal.pone.0206007?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
    ---><---

    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:plo:pone00:0206007. 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: plosone (email available below). General contact details of provider: https://journals.plos.org/plosone/ .

    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.