Brk/PTK6 and Involucrin Expression May Predict Breast Cancer Cell Responses to Vitamin D3

Int J Mol Sci. 2023 Jun 28;24(13):10757. doi: 10.3390/ijms241310757.

Abstract

The process of human embryonic mammary development gives rise to the structures in which mammary cells share a developmental lineage with skin epithelial cells such as keratinocytes. As some breast carcinomas have previously been shown to express high levels of involucrin, a marker of keratinocyte differentiation, we hypothesised that some breast tumours may de-differentiate to a keratinocyte-derived 'evolutionary history'. To confirm our hypothesis, we investigated the frequency of involucrin expression along with that of Brk, a tyrosine kinase expressed in up to 86% of breast carcinomas whose normal expression patterns are restricted to differentiating epithelial cells, most notably those in the skin (keratinocytes) and the gastrointestinal tract. We found that involucrin, a keratinocyte differentiation marker, was expressed in a high proportion (78%) of breast carcinoma samples and cell lines. Interestingly, tumour samples found to express high levels of involucrin were also shown to express Brk. 1,25-dihydroxyvitamin D3, a known differentiation agent and potential anti-cancer agent, decreased proliferation in the breast cancer cell lines that expressed both involucrin and Brk, whereas the Brk/involucrin negative cell lines tested were less susceptible. In addition, responses to 1,25-dihydroxyvitamin D3 were not correlated with vitamin D receptor expression. These data contribute to the growing body of evidence suggesting that cellular responses to 1,25-dihydroxyvitamin D3 are potentially independent of vitamin D receptor status and provide an insight into potential markers, such as Brk and/or involucrin that could predict therapeutic responses to 1,25-dihydroxyvitamin D3.

Keywords: 1,25-dihydroxyvitamin D3; breast cancer; breast tumour kinase (Brk); differentiation; involucrin; protein tyrosine kinase 6 (PTK6).

MeSH terms

  • Breast Neoplasms* / metabolism
  • Calcitriol
  • Cholecalciferol
  • Female
  • Humans
  • Neoplasm Proteins / metabolism
  • Protein-Tyrosine Kinases
  • Receptors, Calcitriol*

Substances

  • Receptors, Calcitriol
  • involucrin
  • Cholecalciferol
  • Calcitriol
  • PTK6 protein, human
  • Neoplasm Proteins
  • Protein-Tyrosine Kinases