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In this context, the investigation employed A2780 and IGROV1 cells, along with their cisplatin-resistant counterparts, A2780/CP70 and IGROV1-R10, to explore SFNs potential in overcoming cisplatin resistance

[1] The cyclic disulfide structure is thought to contribute to conformational rigidity and resistance to peptide degradation in biological environments. Pharmacokinetic studies in murine plasma indicated a plasma half-life of approximately 4 minutes under in vitro conditions, reflecting rapid enzymatic metabolism of the peptide backbone

Quantification of the glutathione redox potential in triple clt1 clt2 clt3 mutants, perturbed in chloroplast envelope glutathione transport, revealed an increase of about 20 mV in the cytosol while the plastidial potential was not affected (Maughan et al., 2010)

95% CI, 2.0511.41), with persistence of increased risk in the emphysema group without bronchial obstruction (OR =4.33