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Truncated WT1 Protein Isoform Expression Is Increased in MCF-7 Cells with Long-Term Estrogen Depletion.

Saavedra-Alonso SantiagoZapata-Benavides PabloMendoza-Gamboa EdgarChavez-Escamilla Ana KarinaArellano-Rodríguez MarielaRodriguez-Padilla Cristina
Published in: International journal of breast cancer (2021)
Modulation of protein isoforms showed differential expression of WT1 isoforms dependent on estrogen receptor. The absence of 52-54 kDa and the presence of the 36-38 kDa protein isoform of WT1 were detected in ER-negative breast cancer cell lines classified as advanced stage cells. Long-term estrogen depletion assay in MCF-7 cells increased the expression of the 36-38 kDa isoform and reduced the 52-54 kDa isoform, and these cells show an increase in the expression of tumor markers of ER and Her2/neu. MCF-7 LTED cells showed low proliferation and insensitivity to tamoxifen compared to MCF-7 cells in normal conditions. These results support the theory about the relationship of the 36-38 kDa isoform of WT1 and the absence of ER function in advanced breast cancer.
Keyphrases
  • induced apoptosis
  • estrogen receptor
  • cell cycle arrest
  • breast cancer cells
  • poor prognosis
  • signaling pathway
  • oxidative stress
  • binding protein
  • heat shock protein
  • cell death
  • small molecule
  • cell proliferation