The potential role of the heparin-binding growth factor pleiotrophin in breast cancer

Breast Cancer Res Treat. 1994;31(2-3):309-14. doi: 10.1007/BF00666163.

Abstract

We propose that the secreted protein pleiotrophin (PTN) is a major factor in the malignant progression of breast cancer. This hypothesis is based on the growth-stimulatory effects of PTN on cells in vitro and in vivo and on its high levels of expression in 60% of tumor samples from breast cancer patients. The stimulation of proliferation and tube formation of endothelial cells by PTN suggests that it can serve as an angiogenesis factor during tumor growth. We hypothesize that PTN has the potential to support growth of breast cancer at its primary site and to enhance the ability of tumor cells to metastasize. Furthermore, we suggest that specific endocrine signals interact to regulate the expression of PTN in vitro and in vivo. Finally, we propose that understanding the functions of PTN and its hormonal regulation can lead to the development of novel therapeutic strategies for breast cancer.

Publication types

  • Review

MeSH terms

  • Breast Neoplasms / genetics
  • Breast Neoplasms / metabolism
  • Breast Neoplasms / pathology*
  • Carrier Proteins / biosynthesis
  • Carrier Proteins / genetics
  • Carrier Proteins / pharmacology
  • Carrier Proteins / physiology*
  • Cell Division / drug effects
  • Cytokines / biosynthesis
  • Cytokines / genetics
  • Cytokines / pharmacology
  • Cytokines / physiology*
  • Gene Expression Regulation, Neoplastic / drug effects
  • Growth Substances / physiology
  • Humans
  • Neoplasm Metastasis / physiopathology
  • Neoplasm Proteins / biosynthesis
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / physiology*
  • Neovascularization, Pathologic / physiopathology
  • Receptors, Estrogen / physiology
  • Receptors, Progesterone / physiology
  • Tamoxifen / pharmacology
  • Tretinoin / pharmacology
  • Tumor Cells, Cultured / drug effects

Substances

  • Carrier Proteins
  • Cytokines
  • Growth Substances
  • Neoplasm Proteins
  • Receptors, Estrogen
  • Receptors, Progesterone
  • Tamoxifen
  • pleiotrophin
  • Tretinoin