| Literature DB >> 22559865 |
Carlos Turrado1, Teresa Puig, Javier García-Cárceles, Marta Artola, Bellinda Benhamú, Silvia Ortega-Gutiérrez, Joana Relat, Gloria Oliveras, Adriana Blancafort, Diego Haro, Pedro F Marrero, Ramón Colomer, María L López-Rodríguez.
Abstract
Fatty acid synthase (FASN) is a lipogenic enzyme that is highly expressed in different human cancers. Here we report the development of a new series of polyphenolic compounds 5-30 that have been evaluated for their cytotoxic capacity in SK-Br3 cells, a human breast cancer cell line with high FASN expression. The compounds with an IC(50) < 50 μM have been tested for their ability to inhibit FASN activity. Among them, derivative 30 blocks the 90% of FASN activity at low concentration (4 μM), is highly cytotoxic in a broad panel of tumor cells, induces apoptosis, and blocks the activation of HER2, AKT, and ERK pathways. Remarkably, 30 does not activate carnitine palmitoyltransferase-1 (CPT-1) nor induces in mice weight loss, which are the main drawbacks of other previously described FASN inhibitors. Thus, FASN inhibitor 30 may aid the validation of this enzyme as a therapeutic target for the treatment of cancer.Entities:
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Year: 2012 PMID: 22559865 DOI: 10.1021/jm2016045
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446