AXL is crucial for E1A-enhanced therapeutic efficiency of EGFR tyrosine kinase inhibitors through NFI in breast cancer

  • Chih Ming Su
  • , Tung Wei Hsu
  • , Shian Ying Sung
  • , Ming Te Huang
  • , Kuan Chou Chen
  • , Chih Yang Huang
  • , Chien Yi Chiang
  • , Yen Hao Su*
  • , Hsin An Chen*
  • , Po Hsiang Liao*
  • *Corresponding author for this work

    Research output: Contribution to journalJournal articlepeer-review

    4 Citations (Scopus)

    Abstract

    AXL which is a chemosensitizer protein for breast cancer cells in response to epidermal growth factor receptor-tyrosine kinase inhibitor and suppresses tumor growth. The clinical information show nuclear factor I (NFI)-C and NFI-X expression correlate with AXL expression in breast cancer patients. Following, we establish serial deletions of AXL promoter to identify regions required for Adenovirus-5 early region 1A (E1A)-mediated AXL suppression. All of the NFI family members were extensively studied for their expression and functions in regulating AXL. Moreover, E1A post-transcriptionally downregulates AXL expression through NFI. NFI-C and NFI-X, not NFI-A and NFI-B, resulting in cell death in response to EGFR-TKI. Our finding suggests that NFI-C and NFI-X are crucial regulators for AXL and significantly correlated with poor survival of breast cancer patients.

    Original languageEnglish
    Pages (from-to)1278-1287
    Number of pages10
    JournalEnvironmental Toxicology
    Volume36
    Issue number7
    Early online date18 Mar 2021
    DOIs
    Publication statusPublished - Jul 2021

    User-Defined Keywords

    • AXL
    • breast cancer
    • EGFR tyrosine kinase inhibitor
    • nuclear factor I

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