Syndecan-1 could be added to hormonal receptors and HER2/neu in routine assessment of invasive breast carcinoma, relation of its expression to prognosis and clinicopathological parameters

Pathol Res Pract. 2019 May;215(5):977-982. doi: 10.1016/j.prp.2019.02.003. Epub 2019 Feb 2.

Abstract

Introduction: Syndecan-1 is heparan sulfate proteoglycans (HSPGs) that is used as coreceptors for signaling of growth factors. The comprehensive effect of syndecan-1 is to augment receptor stimulation at little ligand concentrations. THE GOAL OF THIS RESEARCH: is to study syndecan-1 expression in breast carcinoma and its value in predicting the prognosis in comparison to other clinicopathological parameters. MATERIAL &METHODS: immunohistochemistry study for syndecan-1 is done on 103 cases of invasive breast carcinoma. Its expression is assessed and correlated to other clinicopathological parameters and prognosis.

Results: overexpression was significantly related to high histologic grade (p = 0.001), large tumor size (p = 0.043), HER2-positive status (p = 0.001), and ER&PR-negative status (p = 0.001). It was also have a negative impact on the overall survival (p=0.012) and disease free survival (p = 0.009). Syndecan-1 expression showed weak positive correlation with Her 2 expression (Correlation Coefficient (co): 0.332, p = 0.001).

Conclusion: syndecan-1 is a good predictor of poor overall survival and recurrence/ metastasis free survival. It is associated with aggressive phenotype as HER2 enriched and Triple negative rather than luminal subtypes of breast carcinoma. So it can be added to the hormonal receptors and HER 2 assay in the routine management of invasive breast cancer after confirmation on a more larger study.

Keywords: Breast carcinoma; HER2; HSPGs; Immunohistochemistry; Syndecan-1.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Biomarkers, Tumor / analysis*
  • Breast Neoplasms / mortality
  • Breast Neoplasms / pathology*
  • Carcinoma / mortality
  • Carcinoma / pathology*
  • Disease-Free Survival
  • Female
  • Humans
  • Middle Aged
  • Prognosis
  • Receptor, ErbB-2 / analysis
  • Receptor, ErbB-2 / biosynthesis
  • Receptors, Estrogen / analysis
  • Receptors, Estrogen / biosynthesis
  • Receptors, Progesterone / analysis
  • Receptors, Progesterone / biosynthesis
  • Retrospective Studies
  • Syndecan-1 / analysis
  • Syndecan-1 / biosynthesis*

Substances

  • Biomarkers, Tumor
  • Receptors, Estrogen
  • Receptors, Progesterone
  • SDC1 protein, human
  • Syndecan-1
  • ERBB2 protein, human
  • Receptor, ErbB-2