| Literature DB >> 25256790 |
Jürgen Eirich1, Simone Braig, Liliana Schyschka, Phil Servatius, Judith Hoffmann, Sabrina Hecht, Simone Fulda, Stefan Zahler, Iris Antes, Uli Kazmaier, Stephan A Sieber, Angelika M Vollmar.
Abstract
Resistance to chemotherapeutic agents represents a major challenge in cancer research. One approach to this problem is combination therapy, the application of a toxic chemotherapeutic drug together with a sensitizing compound that addresses the vulnerability of cancer cells to induce apoptosis. Here we report the discovery of a new compound class (T8) that sensitizes various cancer cells towards etoposide treatment at subtoxic concentrations. Proteomic analysis revealed protein disulfide isomerase (PDI) as the target of the T8 class. In-depth chemical and biological studies such as the synthesis of optimized compounds, molecular docking analyses, cellular imaging, and apoptosis assays confirmed the unique mode of action through reversible PDI inhibition.Entities:
Keywords: cancer; chemotherapeutics; combination therapy; proteomics; sensitization
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Year: 2014 PMID: 25256790 DOI: 10.1002/anie.201406577
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336