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Freire, T. S.

Publications and source records attributed to Freire, T. S..

2 recordsLinked to original sources

Ebselen protects XPC deficient cells through a potentially mitohormetic mechanism

Xeroderma pigmentosum group C fiborblasts (XP-C) are characterized by chronic redox imbalance and elevated H{square}O{square}levels, making them a good model for testing compounds with antioxidant potential for therapeutic purposes. Here, we investigated the effects of ebselen, a compound with glutathione peroxidase (GPx) mimetic activity, in the XP-C model. We found that ebselen behaves as a hormetic compound, protecting cells against H2O2-induced cytotoxicity at low doses but potentiating the cytotoxic effect at higher doses. Accordingly, when administered chronically, ebselen significantly reduces H{square}O{square}production and p53 levels. However, acute treatment with ebselen causes a reduction in O2 consumption (OCR) and extracellular acidification rate (ECAR), indicative of decreased mitochondrial function and metabolic activity. In addition, acute ebselen treatment causes a reduction in the GSH/GSSG ratio and an increase in NRF-2 expression, suggesting that ebselen induces redox stress that triggers an adaptive response, characterizing a possible mitohormetic effect. The reduction in the GSH/GSSG ratio appears to be the initial trigger after acute treatment with ebselen, since concomitant treatment with NAC prevents the reduction in OCR, ECAR and NRF-2 activation, in addition to protecting XP-C cells against lethal doses of ebselen. HighlightsO_LIChronic ebselen treatment reduces H2O2 levels, lowers p53 expression and protects XP-C cells against oxidative insults. C_LIO_LIInitially, ebselen causes mitochondrial stress, which is followed by cellular adaptation and protection against oxidative stress. C_LIO_LIEbselen acts as a hormetic drug, likely through a mitohormetic mechanism. C_LI

biochemistry↗

Beyond IC50 - A computational dynamic model of drug resistance in enzyme inhibition treatment.

Resistance to therapy is a major clinical obstacle to treatment of cancer and communicable diseases. Chronic myeloid leukaemia (CML) is a blood cancer that is treated with Abl1 inhibitors, and is often seen as a model for targeted therapy and drug resistance. Resistance to the first-line treatment occurs in approximately one in four patients. The most common cause of resistance is mutations in the Abl1 enzyme. Different mutant Abl1 enzymes show resistance to different Abl1 inhibitors and the mechanisms that lead to resistance for various mutation and inhibitor combinations are not fully known, making the selection of Abl1 inhibitors for treatment a difficult task. We developed a model based on information of catalysis, inhibition and pharmacokinetics, and applied it to study the effect of three Abl1 inhibitors on mutants of the Abl1 enzyme. From this model, we show that the relative decrease of product formation rate (defined in this work as "inhibitory reduction prowess") is a better indicator of resistance than an examination of the size of the product formation rate or fold-IC50 values for the mutant. We also examine current ideas and practices that guide treatment choice and suggest a new parameter for selecting treatments that could increase the efficacy and thus have a positive impact on patient outcomes.

biophysics↗