| Literature DB >> 32223240 |
Luca Quattrini1, Edoardo Luigi Maria Gelardi2, Vito Coviello1, Stefania Sartini1, Davide Maria Ferraris2, Mattia Mori3, Ichiro Nakano4, Silvia Garavaglia2, Concettina La Motta1.
Abstract
Glioblastoma multiforme (GBM) is the deadliest form of brain tumor. It is known for its ability to escape the therapeutic options available to date thanks to the presence of a subset of cells endowed with stem-like properties and ability to resist to cytotoxic treatments. As the cytosolic enzyme aldehyde dehydrogenase 1A3 turns out to be overexpressed in these kinds of cells, playing a key role for their vitality, treatments targeting this enzyme may represent a successful strategy to fight GBM. In this work, we describe a novel class of imidazo[1,2-a]pyridine derivatives as aldehyde dehydrogenase 1A3 inhibitors, reporting the evidence of their significance as novel drug candidates for the treatment of GBM. Besides showing an interesting functional profile, in terms of activity against the target enzyme and selectivity toward highly homologous isoenzymes, representative examples of the series also showed a nanomolar to picomolar efficacy against patient-derived GBM stem-like cells, thus proving the concept that targeting aldehyde dehydrogenase might represent a novel and promising way to combat GBM by striking its ability to divide immortally.Entities:
Year: 2020 PMID: 32223240 DOI: 10.1021/acs.jmedchem.9b01910
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446