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Ana Čampa

2 papers in the library · 21 citations · publishing 2013-2014

Papers

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Biosynthesis of N,N-dimethyltryptamine (DMT) in a melanoma cell line and its metabolization by peroxidases.

Biochemical Pharmacology April 1, 2014 Melissa M. Gomes, J. B. Coimbra, R. O. Clara et al. 21 citations

Tryptophan (TRP) is essential for many physiological processes, and its metabolism changes in some diseases such as infection and cancer. The most studied aspects of TRP metabolism are the kynurenine and serotonin pathways. A minor metabolic route, tryptamine and N,N-dimethyltryptamine (DMT) biosynthesis, has received far less attention, probably because of the very low amounts of these...

Tryptamine and dimethyltryptamine inhibit indoleamine 2,3 dioxygenase and increase the tumor-reactive effect of peripheral blood mononuclear cells.

Cell biochemistry and function July 2013 Melissa Cavalheiro Tourino, Edson Mendes De Oliveira, Luziane Potrich Bellé et al.

Indoleamine 2,3-dioxygenase (IDO) is an interferon-γ (IFN-γ)-induced tryptophan-degrading enzyme, producing kynurenine (KYN) that participates in the mechanism of tumor immune tolerance. Thus, IDO inhibition has been considered a strategy for anticancer therapy. The aim of this study was to identify whether the metabolites originated from the competitive routes of tryptophan metabolism, such as...

DOI: 10.1002/cbf.2980 (opens in new tab) Full text (opens in new tab) Immune escape Kynurenine pathway Tolerance Tryptophan metabolism +1