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p95HER2 and Breast Cancer

Journal

CANCER RESEARCH
Volume 71, Issue 5, Pages 1515-1519

Publisher

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/0008-5472.CAN-10-3795

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Funding

  1. Instituto de Salud Carlos III [Intrasalud PI081154]
  2. Network of Cooperative Cancer Research [RTICC-RD06/0020/0022]
  3. Breast Cancer Research Foundation (BCRF)
  4. Asociacion Espanola Contra el Cancer
  5. ICREA Funding Source: Custom

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A subtype of HER2-positive tumors with distinct biological and clinical features expresses a series of carboxyterminal fragments collectively known as p95HER2. One of these fragments, named 100- to 115-kDa p95HER2 or 611-CTF, is hyperactive because of its ability to form homodimers maintained by intermolecular disulfide bonds. Despite lacking the majority of the extracellular domain, this HER2 fragment drives breast cancer progression in vivo. The recent availability of specific anti-p95 antibodies has confirmed previous results indicating that the expression of p95HER2 is predictive of poor prognosis and correlates with resistance to the treatment with trastuzumab, a therapeutic antibody directed against the extracellular domain of HER2. Cancer Res; 71(5); 1515-9. (C)2011 AACR.

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