Expression and Circulating Levels of Perlecan in Breast Cancer - Implications for Oestrogen Dependent Stromal Remodeling

J Mammary Gland Biol Neoplasia. 2020 Mar;25(1):69-77. doi: 10.1007/s10911-020-09447-2. Epub 2020 Mar 2.

Abstract

Localised breast cancer can be cured by surgery and adjuvant treatments, but mortality remains high as some tumours metastasize early. Perlecan is a basement membrane (BM) protein involved in tumour development and progression. Here, mRNA and protein expression of perlecan, and mRNA expression of matrix degrading enzymes were studied in normal breast and invasive breast cancer, and correlated to prognostic risk factors, in particular oestrogen status. Moreover, plasma levels of perlecan were measured in patients with breast cancer and compared with controls. mRNA data was extracted from the Cancer Genome Atlas database. Perlecan protein expression was visualized using immunofluorescence and plasma levels measured by ELISA assay. Perlecan mRNA levels were twice as high in normal breast compared with breast cancer tissue. A strong correlation was found between mRNA expression of perlecan and several matrix-degrading enzymes in oestrogen receptor positive (ER+) tumours. Perlecan protein was localized to both epithelial and vascular BMs, but absent in the stroma in normal breast. In breast cancer, the expression of perlecan in epithelial BM was fragmented or completely lost, with a marked upregulation of perlecan expression in the stroma. Significantly higher levels of perlecan were found in plasma of ER+ patients when compared with ER- patients. This study shows that perlecan expression and degradation in breast cancer may be linked to the ER status of the tumour.

Keywords: Breast cancer; Matrix metalloproteinases; Oestrogen receptor, extracellular matrix; Perlecan/HSPG2.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers, Tumor / blood*
  • Biomarkers, Tumor / genetics
  • Breast Neoplasms / blood
  • Breast Neoplasms / genetics
  • Breast Neoplasms / pathology*
  • Carcinoma, Ductal, Breast / blood
  • Carcinoma, Ductal, Breast / genetics
  • Carcinoma, Ductal, Breast / pathology*
  • Carcinoma, Lobular / blood
  • Carcinoma, Lobular / genetics
  • Carcinoma, Lobular / pathology*
  • Case-Control Studies
  • Cohort Studies
  • Extracellular Matrix Proteins / genetics
  • Extracellular Matrix Proteins / metabolism
  • Female
  • Follow-Up Studies
  • Heparan Sulfate Proteoglycans / blood*
  • Heparan Sulfate Proteoglycans / genetics
  • Humans
  • Middle Aged
  • Prognosis
  • Receptor, ErbB-2 / metabolism
  • Receptors, Estrogen / metabolism*
  • Receptors, Progesterone / metabolism
  • Stromal Cells / metabolism*
  • Stromal Cells / pathology

Substances

  • Biomarkers, Tumor
  • Extracellular Matrix Proteins
  • Heparan Sulfate Proteoglycans
  • Receptors, Estrogen
  • Receptors, Progesterone
  • perlecan
  • ERBB2 protein, human
  • Receptor, ErbB-2