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Merck

Desmethylclomipramine induces the accumulation of autophagy markers by blocking autophagic flux.

Journal of cell science (2009-08-27)
Mario Rossi, Eliana Rosa Munarriz, Stefano Bartesaghi, Marco Milanese, David Dinsdale, Maria Azucena Guerra-Martin, Edward T W Bampton, Paul Glynn, Giambattista Bonanno, Richard A Knight, Pierluigi Nicotera, Gerry Melino
ABSTRAKT

Alterations in the autophagic pathway are associated with the onset and progression of various diseases. However, despite the therapeutic potential for pharmacological modulators of autophagic flux, few such compounds have been characterised. Here we show that clomipramine, an FDA-approved drug long used for the treatment of psychiatric disorders, and its active metabolite desmethylclomipramine (DCMI) interfere with autophagic flux. Treating cells with DCMI caused a significant and specific increase in autophagosomal markers and a concomitant blockage of the degradation of autophagic cargo. This observation might be relevant in therapy in which malignant cells exploit autophagy to survive stress conditions, rendering them more susceptible to the action of cytotoxic agents. In accordance, DCMI-mediated obstruction of autophagic flux increased the cytotoxic effect of chemotherapeutic agents. Collectively, our studies describe a new function of DCMI that can be exploited for the treatment of pathological conditions in which manipulation of autophagic flux is thought to be beneficial.

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Sigma-Aldrich
Norclomipramine hydrochloride, ≥98% (TLC), powder
Supelco
N-Desmethylclomipramine hydrochloride solution, 1.0 mg/mL in methanol (as free base), ampule of 1 mL, certified reference material, Cerilliant®