Development of a Benzoxazine-derived Inhibitor Targeting Epithelial-to-Mesenchymal Transition in Lung Cancer

Naphatson Phansom1,2, Zin Zin Ei2,3, Bhurichaya Innets2,3

  • 1Graduate Program of Biomedical Sciences, Faculty of Science, Rangsit University, Pathumthani, Thailand.

Anticancer Research
|June 27, 2025
PubMed
Abstract

Insights

The novel compound 2,4-diMBD inhibits epithelial-mesenchymal transition (EMT) in lung cancer cells. This compound shows promise for reducing lung cancer metastasis by suppressing key EMT markers.

Area of Science:

  • Oncology
  • Molecular Biology
  • Cancer Research

Background:

  • Epithelial-mesenchymal transition (EMT) is crucial for lung cancer metastasis.
  • Targeting EMT is a potential therapeutic strategy for lung cancer.

Purpose of the Study:

  • To investigate the EMT inhibitory effects of a new compound, 6,6'-(butylazanediyl) bis (methylene) bis (2,4-dimethylphenol) (2,4-diMBD).
  • To evaluate the anti-metastatic potential of 2,4-diMBD in human lung cancer cells.

Main Methods:

  • Cell viability, colony formation, and wound-healing assays were used to assess cell proliferation and migration.
  • Immunofluorescence and real-time quantitative PCR were employed to examine protein and mRNA expression levels.

Main Results:

  • 2,4-diMBD significantly inhibited lung cancer cell colony formation and migration.
  • The compound reduced the expression of key EMT markers, including Snail, Slug, and ZEB, at both mRNA and protein levels.
  • These findings indicate that 2,4-diMBD suppresses EMT in lung cancer cells.

Conclusions:

  • 2,4-diMBD demonstrates anti-metastatic properties in lung cancer by inhibiting EMT.
  • The compound represents a promising therapeutic candidate for lung cancer treatment.