VGLL1 stabilization of cytoplasmic TAZ promotes EGFR expression and maintains tumor initiating cells in breast cancer independent of TEAD

Cell Signal. 2024 Jun:118:111120. doi: 10.1016/j.cellsig.2024.111120. Epub 2024 Feb 28.

Abstract

Vestigial-like family member 1 (VGLL1) is one of the X-linked genes whose expression is elevated in basal-like breast cancer (BLBC) because of X-chromosome isodisomy. As an approach towards understanding its function, we performed correlation study using transcript data of breast cancer patients from cBioPortal for Cancer Genomics. Our analysis identified EGFR as the most correlated transcript with VGLL1. We demonstrate that VGLL1 promotes EGFR expression and increases the frequency of breast tumor initiating cells (CD44high/+CD24low/-). These findings are crucial because an elevated EGFR expression and high frequency of CD44high/+CD24low/- cells are defining features of BLBC, and we provide a new mechanistic insight into how their expressions are controlled. Importantly, VGLL1 regulation of EGFR and CD44high/+CD24low/- population is mediated by the hippo-transducer TAZ which exerts its oncogenic roles by binding and activating TEAD transcription factors. A crucial finding is that TEAD-binding domain of TAZ is dispensable for its regulation of EGFR and CD44high/+CD24low/- cells. Instead, VGLL1 stabilization of cytoplasmic TAZ is essential for these functions. Also, we show that VGLL1/TAZ restricts the surface expression of CD24 which contributes to the increased number of CD44high/+CD24low/- cells. In addition, we observed that VGLL1 represses AXL expression and suppresses claudin-low phenotype, and that is caused by the VGLL1 mediated nuclear expulsion of TAZ. Therefore, EGFR and AXL seem to represent two different breast tumor subtypes, and their differential expressions is controlled by VGLL1.

Keywords: AXL; Basal-like breast cancer; EGFR; TAZ; VGLL1.

MeSH terms

  • Breast Neoplasms* / pathology
  • CD24 Antigen / metabolism
  • Cytoplasm / metabolism
  • DNA-Binding Proteins / metabolism
  • ErbB Receptors / genetics
  • ErbB Receptors / metabolism
  • Female
  • Humans
  • Hyaluronan Receptors / metabolism
  • Neoplastic Stem Cells / metabolism
  • Transcription Factors / metabolism

Substances

  • CD24 Antigen
  • DNA-Binding Proteins
  • EGFR protein, human
  • ErbB Receptors
  • Hyaluronan Receptors
  • Transcription Factors
  • VGLL1 protein, human
  • WWTR1 protein, human