Tumor escape and progression of HER-2/neu negative breast cancer under immune pressure

J Transl Med. 2011 Mar 31:9:35. doi: 10.1186/1479-5876-9-35.

Abstract

Background: Emerging data from pre-clinical and clinical studies suggest that HER-2/neu-specific T cell responses could induce HER-2/neu antigen loss in the tumor cells. These data suggest that patients with HER-2/neu negative breast cancer might have had HER-2/neu positive premalignant lesions in the past that progressed to HER-2/neu negative breast cancer under HER-2/neu-specific immune pressure.

Methods: We conducted a pilot study in patients with HER-2/neu positive and HER-2/neu negative breast cancers as well as a patient with ductal carcinoma in situ (DCIS). HER-2/neu expression was determined by FISH. HER-2/neu-specific T cell responses were determined by using IFN-γ ELISA. Expression of IFN-γ Rα in the tumors was determined by immunohistochemistry analysis of paraffin-embedded tissues.

Results: We determined that majority of (10 of 12) patients with HER-2/neu negative breast cancer had HER-2/neu-specific IFN-γ producing T cell responses which was stronger than those in patients with HER-2/neu positive tumors. Such immune responses were associated with nuclear translocation of IFN-γ Rα in their tumor cells. Patient with DCIS also showed HER-2/neu-specific T cell responses.

Conclusion: These data suggest that conducting retrospective studies in patients with HER-2/neu negative breast cancers and prospective studies in patients with HER-2/neu positive DCIS can determine whether HER-2/neu negative invasive carcinomas arise from HER-2/neu positive DCIS under the immune pressure.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Breast Neoplasms / immunology*
  • Breast Neoplasms / pathology*
  • Cell Line, Tumor
  • Cell Nucleus / metabolism
  • Disease Progression*
  • Female
  • Humans
  • Interferon gamma Receptor
  • Interferon-gamma / metabolism
  • Protein Transport
  • Receptor, ErbB-2 / metabolism*
  • Receptors, Interferon / metabolism
  • T-Lymphocytes / immunology
  • Tumor Escape / immunology*

Substances

  • Receptors, Interferon
  • Interferon-gamma
  • ERBB2 protein, human
  • Receptor, ErbB-2