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Discovery of a septin-4 covalent binder with antimetastatic activity in a mouse model of melanoma

  • Federica Blua
  • , Chiara Monge
  • , Simone Gastaldi
  • , Nausicaa Clemente
  • , Stefania Pizzimenti
  • , Loretta Lazzarato
  • , Rebecca Senetta
  • , Serena Vittorio
  • , Casimiro Luca Gigliotti
  • , Elena Boggio
  • , Umberto Dianzani
  • , Giulio Vistoli
  • , Alessandra Anna Altomare
  • , Giancarlo Aldini
  • , Chiara Dianzani
  • , Elisabetta Marini
  • , Massimo Bertinaria

Research output: Contribution to journalArticlepeer-review

Abstract

Cancer spreading through metastatic processes is one of the major causes of tumour-related mortality. Metastasis is a complex phenomenon which involves multiple pathways ranging from cell metabolic alterations to changes in the biophysical phenotype of cells and tissues. In the search for new effective anti-metastatic agents, we modulated the chemical structure of the lead compound AA6, in order to find the structural determinants of activity, and to identify the cellular target responsible of the downstream anti-metastatic effects observed. New compounds synthesized were able to inhibit in vitro B16-F10 melanoma cell invasiveness, and one selected compound, CM365, showed in vivo anti-metastatic effects in a lung metastasis mouse model of melanoma. Septin-4 was identified as the most likely molecular target responsible for these effects. This study showed that CM365 is a promising molecule for metastasis prevention, remarkably effective alone or co-administered with drugs normally used in cancer therapy, such as paclitaxel.

Original languageEnglish
Article number107164
JournalBioorganic Chemistry
Volume144
DOIs
Publication statusPublished - Mar 2024

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Anti-metastatic agents
  • Cancer dissemination
  • Invasiveness inhibition
  • Peptide mapping
  • Septin-4

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