These factors were calculated by integrating the A280 values from the polysome tracings selelck kinase inhibitor for the appropriate fractions from multiple independent experiments on WT and mutant extracts, yielding the following average values, HPWT 0. 308, HP4G 0. 114, LPWT 0. 276, LP4G 0. 149, 80SWT 0. 416, 80S4G 0. 738. Cisplatin is an effective antitumor agent widely used for the treatment of different tumor types. In spite of the efficacy, the curative poten tial of such an antitumor drug is limited by the occurrence of resistance. Most information about genetic alterations and cellular mechanisms contributing to drug response resistance comes from mammalian cell systems. Several mechanisms of resistance to cisplatin have been described including reduced drug accumulation, enhanced repair and increased expression of defence factors.
Some lines of evidence support the concept that altered expression of sub sets of genes may be important in determining Inhibitors,Modulators,Libraries the sensitiv ity resistance to antitumor agents including cisplatin. Given the powerful molecular tools now available, the com bination of molecular pharmacology and molecular biology approaches in studying model organisms could lead to a rapid progress in the discovery of strategies to overcome drug resistance. The ease by which yeast can be manipulated together with similarities of yeast cells to cells of more com plex metazoans makes many yeast species, very attractive models for the investigation of conserved evolutionary processes occurring in eukaryotes. Using DNA microarrays, we previously found that in fission yeast cisplatin activates a stress response involving various gene groups.
In particu lar, among the transcripts up regulated by cisplatin in the sensitive strain, several genes Inhibitors,Modulators,Libraries belonging to the ubiquitin proteasome pathway were identified. The Ub proteasome pathway is implicated in the regula tion of a variety of cellular functions and plays a major role in stress response. In fact, by degrading misfolded and damaged proteins, the pathway controls processes includ ing cell cycle, cell death and DNA repair. The protea some recognizes ubiquitinated substrates through its Ub receptors and digest them into peptides and free Ubs. The pathway includes Ub activating enzymes, Ub conju gating enzymes and Ub ligases, all acting in con cert to tag substrates with Ub chains.
Proteins may be monoubiquitinated or the Ub monomer may act as a point of attachment for additional Ub monomers, result ing in polyubiquitination. The specific biological signal mediated by a polyubiquitin chain is determined, in part, by the chain topology, which is assigned by the Ub lysine Inhibitors,Modulators,Libraries residue used for chain extension. Inhibitors,Modulators,Libraries Lys48 linked chains have been implicated in targeting proteins for proteasomal degradation, whereas Lys63 linked chains seem to regulate proteins involved in a wide range of processes, including DNA Inhibitors,Modulators,Libraries repair, mRNA translation inhibitor Aurora Kinase Inhibitor and endocytosis.