Increased natural killer cell activity correlates with low or negative expression of the HER-2/neu oncogene in patients with breast cancer

Cancer. 1994 Jan 1;73(1):135-9. doi: 10.1002/1097-0142(19940101)73:1<135::aid-cncr2820730123>3.0.co;2-s.

Abstract

Background: Increased expression of the HER-2/neu oncogene in breast cancer correlates with decreased estrogen receptor concentration and seems to be an important prognostic factor. The authors investigated whether there is a correlation between HER-2/neu expression and immunologic parameters representing tumor defense in patients with breast cancer.

Method: A Western blot analysis was used to investigate HER-2/neu expression, whereas a chromium-release assay using the K562 cell line as target was used to measure natural killer (NK) cell activity.

Results: In patients with breast cancer, NK cell activity was significantly higher compared with patients with benign tumors (P = 0.006) or healthy control subjects (P = 0.002). Moreover, 23.3% of patients with breast cancer showed an overexpression of HER-2/neu protein. Within this group of patients, NK cell activity was significantly lower (45.6 +/- 16.1%) compared with the group with no HER-2/neu overexpression (57.3 +/- 11.0%). NK cell activity did not increase in patients with HER-2/neu overexpression. Thus, there was a statistically significant correlation of cytolytic effector cell function with HER-2/neu expression of the tumor (P = 0.003), and HER-2/neu overexpression correlated with a negative estrogen receptor status (P = 0.005).

Conclusion: These data add further evidence to previous observations from the authors' laboratory that certain tumor characteristics may be associated with reactions of the host with breast cancer.

MeSH terms

  • Breast / pathology
  • Breast Diseases / genetics
  • Breast Diseases / pathology
  • Breast Neoplasms / blood
  • Breast Neoplasms / genetics*
  • Breast Neoplasms / pathology*
  • Case-Control Studies
  • Female
  • Gene Expression Regulation, Neoplastic / genetics*
  • Humans
  • Killer Cells, Natural / physiology*
  • Oncogene Proteins, Viral / analysis
  • Oncogene Proteins, Viral / genetics*
  • Oncogenes / genetics*
  • Receptor, ErbB-2
  • Receptors, Estrogen / analysis
  • Receptors, Estrogen / genetics
  • Receptors, Progesterone / analysis
  • Receptors, Progesterone / genetics

Substances

  • Oncogene Proteins, Viral
  • Receptors, Estrogen
  • Receptors, Progesterone
  • Receptor, ErbB-2