Clinical Epigenetics (Dec 2023)

In-silico guided chemical exploration of KDM4A fragments hits

  • Jessica Lombino,
  • Rosario Vallone,
  • Maura Cimino,
  • Maria Rita Gulotta,
  • Giada De Simone,
  • Maria Agnese Morando,
  • Raffaele Sabbatella,
  • Simona Di Martino,
  • Mario Fogazza,
  • Federica Sarno,
  • Claudia Coronnello,
  • Maria De Rosa,
  • Chiara Cipollina,
  • Lucia Altucci,
  • Ugo Perricone,
  • Caterina Alfano

DOI
https://doi.org/10.1186/s13148-023-01613-7
Journal volume & issue
Vol. 15, no. 1
pp. 1 – 16

Abstract

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Abstract Background Lysine demethylase enzymes (KDMs) are an emerging class of therapeutic targets, that catalyse the removal of methyl marks from histone lysine residues regulating chromatin structure and gene expression. KDM4A isoform plays an important role in the epigenetic dysregulation in various cancers and is linked to aggressive disease and poor clinical outcomes. Despite several efforts, the KDM4 family lacks successful specific molecular inhibitors. Results Herein, starting from a structure-based fragments virtual screening campaign we developed a synergic framework as a guide to rationally design efficient KDM4A inhibitors. Commercial libraries were used to create a fragments collection and perform a virtual screening campaign combining docking and pharmacophore approaches. The most promising compounds were tested in-vitro by a Homogeneous Time-Resolved Fluorescence-based assay developed for identifying selective substrate-competitive inhibitors by means of inhibition of H3K9me3 peptide demethylation. 2-(methylcarbamoyl)isonicotinic acid was identified as a preliminary active fragment, displaying inhibition of KDM4A enzymatic activity. Its chemical exploration was deeply investigated by computational and experimental approaches which allowed a rational fragment growing process. The in-silico studies guided the development of derivatives designed as expansion of the primary fragment hit and provided further knowledge on the structure–activity relationship. Conclusions Our study describes useful insights into key ligand-KDM4A protein interaction and provides structural features for the development of successful selective KDM4A inhibitors.

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