PCNA/cyclin and P-glycoprotein as prognostic factors in locally advanced breast cancer. An immunohistochemical, retrospective study

Tumori. 1993 Jun 30;79(3):214-8. doi: 10.1177/030089169307900312.

Abstract

Aims and background: The aim of the present study was to determine, retrospectively, whether the immunohistochemical expression of two biologic markers of aggressively, P-glycoprotein (P-gp) and PCNA/cyclin (PCNA), could be related to response to chemotherapy and prognosis in locally advanced breast cancer.

Methods: PC 10 Mab was used to determine the proliferation index (PCNA) and C-219 Mab to determine P-gp in 25 locally advanced breast carcinomas subjected to preoperative chemotherapy with MDR-related drugs.

Results: P-gp and PCNA were expressed in 76% and 100% of the tumors, respectively. No case of high P-gp expression was associated with good chemosensitivity, and all P-gp-negative cases showed the best chemotherapeutic response. P-gp and PCNA were both highly expressed in patients who developed local-regional or distant metastases. No recurrence was associated with a negative or low P-gp score.

Conclusions: Statistical analysis showed that high P-gp expression was related to a poor response to chemotherapy and a short disease-free survival. A high PCNA score was not found to be significant for predicting chemosensitivity or survival.

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Adult
  • Antigens, Neoplasm / analysis*
  • Biomarkers / analysis
  • Breast Neoplasms / chemistry*
  • Breast Neoplasms / drug therapy
  • Breast Neoplasms / mortality
  • Breast Neoplasms / pathology
  • Carrier Proteins / analysis*
  • Humans
  • Immunohistochemistry
  • Membrane Glycoproteins / analysis*
  • Middle Aged
  • Neoplasm Proteins / analysis*
  • Nuclear Proteins / analysis*
  • Prognosis
  • Proliferating Cell Nuclear Antigen
  • Retrospective Studies
  • Survival Analysis

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Antigens, Neoplasm
  • Biomarkers
  • Carrier Proteins
  • Membrane Glycoproteins
  • Neoplasm Proteins
  • Nuclear Proteins
  • Proliferating Cell Nuclear Antigen