1. Academic Validation
  2. Anticancer Activities of DNA-Alkylating Pyrrole-Imidazole Polyamide Analogs Targeting RUNX Transcription Factors against p53-Mutated Pancreatic Cancer PANC-1 Cells

Anticancer Activities of DNA-Alkylating Pyrrole-Imidazole Polyamide Analogs Targeting RUNX Transcription Factors against p53-Mutated Pancreatic Cancer PANC-1 Cells

  • J Med Chem. 2023 Sep 14;66(17):12059-12068. doi: 10.1021/acs.jmedchem.3c00613.
Yuki Hirose 1 Shinsuke Sato 1 Kaori Hashiya 1 Toshikazu Bando 1 Hiroshi Sugiyama 1 2
Affiliations

Affiliations

  • 1 Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Kyoto 606-8502, Japan.
  • 2 Institute for Integrated Cell-Material Science (WPI-iCeMS), Kyoto University, Sakyo, Kyoto 606-8501, Japan.
Abstract

The runt-related transcription factor (RUNX) family is known to play important roles in the progression of Cancer. Conjugate 1, which covalently binds to the RUNX-binding sequences, was reported to inhibit the binding of RUNX proteins to their target sites and suppress Cancer growth. Here, we evaluated the Anticancer effects of 1 and its analogs 2-4 against p53-mutated PANC-1 pancreatic Cancer cells. We found that they possessed different DNA-alkylating properties in vitro. And conjugates 1-3 were shown to have Anticancer effects by inducing Apoptosis in PANC-1 cells. Furthermore, conjugates 2 and 3 suppressed Cancer growth in PANC-1 xenograft mice, with activity equivalent to a 50-fold dose of gemcitabine. Especially, 3 showed the highest alkylation efficiency, specificity, and better Anticancer effects against pancreatic Cancer than 1 in vivo without significant body weight loss. Our results revealed the potential of our compounds as new candidates for Cancer therapy.

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