MARCKS protein overexpression is associated with poor prognosis in male breast cancer

Cancer Biomark. 2019;26(4):513-522. doi: 10.3233/CBM-190637.

Abstract

Background: Male breast cancer (MBC) is a rare and aggressive disease. Thus, identification of new therapeutic targets is crucial.

Objective: Our objective was to evaluate the protein expression of MARCKS (Myristoylated Alanine-Rich C-Kinase Substrate) in MBC and to investigate its prognostic value.

Materials and methods: MARCKS protein expression in tumor and stromal cells was analyzed by immunohistochemistry (IHC) in a retrospective series of 96 pre-chemotherapy MBC samples and 80 normal breast samples, from Tunisian patients treated at Salah Azaiez Institute. Correlations were searched between MARCKS expression and clinicopathological features including overall survival (OS).

Results: MARCKS was overexpressed in epithelial tumor cells in 66% of the MBC samples versus 26% of normal samples (p= 1.40 × 10-7). Such positive MARCKS expression in epithelial tumor cells was associated with positive HER2 status (p= 4.0 × 10-3). It was associated with shorter OS in uni-and multivariate analysis. By contrast, stromal IHC MARCKS expression was correlated only with tumor grade.

Conclusion: MARCKS tumor cell overexpression might in part explain the aggressiveness and the poor prognosis of MBC. MARCKS can represent a potential therapeutic target for MBC.

Keywords: MARCKS; expression; immunohistochemistry; male breast cancer; survival.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Breast Neoplasms, Male / genetics
  • Breast Neoplasms, Male / metabolism*
  • Humans
  • Immunohistochemistry
  • Male
  • Middle Aged
  • Myristoylated Alanine-Rich C Kinase Substrate / biosynthesis*
  • Myristoylated Alanine-Rich C Kinase Substrate / genetics
  • Myristoylated Alanine-Rich C Kinase Substrate / metabolism
  • Prognosis
  • Receptor, ErbB-2 / genetics
  • Receptor, ErbB-2 / metabolism
  • Retrospective Studies
  • Survival Rate

Substances

  • MARCKS protein, human
  • Myristoylated Alanine-Rich C Kinase Substrate
  • ERBB2 protein, human
  • Receptor, ErbB-2