Circulating Bmi-1 mRNA as a possible prognostic factor for advanced breast cancer patients

Breast Cancer Res. 2007;9(4):R55. doi: 10.1186/bcr1760.

Abstract

Introduction: Deregulation of Polycomb member Bmi-1 is involved in cell proliferation and human oncogenesis. Modulation of Bmi-1 is found in several tumor tissues, including primary breast carcinomas; however, analysis of Bmi-1 in plasma of cancer patients has not been reported. This is the first study that evaluates Bmi-1 in plasma by using a large series of primary breast carcinomas to investigate the presence at diagnosis of detectable Bmi-1 mRNA in plasma and possible correlations between this event and a series of clinical-pathological parameters of the tumors.

Methods: Bmi-1 expression levels were quantified in plasma of 111 breast cancer patients and in 20 healthy controls by real-time quantitative polymerase chain reaction.

Results: Cancer patients with the presence of Bmi-1 mRNA in plasma had higher levels of Bmi-1 expression than healthy controls with Bmi-1 mRNA in plasma. The higher expression levels of Bmi-1 correlated with well-established markers of poor clinical outcome in breast cancer such as positive p53 immunostaining and negative progesterone receptors. Moreover, we described for the first time a statistically significant correlation between Bmi-1 expression in plasma of breast cancer patients and disease-free and overall survival in advanced stages.

Conclusion: Our results suggest that levels of Bmi-1 expression may be a surrogate marker of poor prognosis and may become clinically useful as noninvasive diagnostic markers.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers, Tumor / genetics
  • Breast Neoplasms / blood*
  • Carcinoma, Ductal, Breast / blood*
  • Carcinoma, Lobular / blood*
  • Case-Control Studies
  • Female
  • Humans
  • Lymphatic Metastasis
  • Neoplasm Invasiveness
  • Neoplasm Staging
  • Neoplastic Cells, Circulating / pathology*
  • Nuclear Proteins / genetics*
  • Polycomb Repressive Complex 1
  • Prognosis
  • Proto-Oncogene Proteins / genetics*
  • RNA, Messenger / blood*
  • RNA, Neoplasm / genetics
  • RNA, Neoplasm / metabolism
  • Receptor, ErbB-2 / metabolism
  • Receptors, Estrogen / metabolism
  • Receptors, Progesterone / metabolism
  • Repressor Proteins / genetics*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Survival Rate

Substances

  • BMI1 protein, human
  • Biomarkers, Tumor
  • Nuclear Proteins
  • Proto-Oncogene Proteins
  • RNA, Messenger
  • RNA, Neoplasm
  • Receptors, Estrogen
  • Receptors, Progesterone
  • Repressor Proteins
  • Polycomb Repressive Complex 1
  • Receptor, ErbB-2