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Chb-M', an Inhibitor of the RUNX Family Binding to DNA, Induces Apoptosis in p53 -Mutated Non-Small Cell Lung Cancer and Inhibits Tumor Growth and Repopulation In Vivo.

Yuki HiroseShinsuke SatoKaori HashiyaMitsuharu OogaToshikazu BandoHiroshi Sugiyama
Published in: Journal of medicinal chemistry (2024)
Runt-related transcription factor (RUNX) proteins are considered to play various roles in cancer. Here, we evaluated the anticancer activity of Chb-M' , a compound that specifically and covalently binds to the consensus sequence for RUNX family proteins, in p53 -mutated non-small cell lung cancer cells. Chb-M' killed the cancer cells by inducing apoptosis. The compound showed an anticancer effect comparable to that of the clinically used drugs alectinib and ceritinib in vivo. Notably, Chb-M' extended the cancer-free survival of mice after ending treatment more effectively than did the other two drugs. The results presented here suggest that Chb-M' is an attractive candidate as an anticancer drug applicable to the treatment of non-small cell lung cancer and various other types of cancers.
Keyphrases
  • transcription factor
  • papillary thyroid
  • free survival
  • squamous cell
  • oxidative stress
  • emergency department
  • stem cells
  • cell therapy
  • clinical practice
  • lymph node metastasis
  • cell proliferation
  • nucleic acid
  • pi k akt