Also, a major effort is required to better understand pathway redundancy because, although ubi quitin ligases have shown a high degree of substrate spe cificity, their inhibition may be counteracted by the activation of alternative pathway components critical for cell survival maintenance. The level of complexity of the Ub proteasome pathway is high as also deubiquitinases can be regarded selleck chemicals Afatinib as druggable targets. More over, the pairing of the pathway components with differ ent substrates may result in divergent activities. In the present study, we identified three Ub protea some mutants exhibiting hypersensitivity to cisplatin, i. e. Ubp16, Ubc13 and Pmt3. Although with very distinct functions, the proteins encoded by those genes play critical roles for DNA damage response, thereby representing attractive targets to investigate possible mechanisms of cisplatin resistance in human tumor cell systems.

With respect to factors whose loss confers cisplatin resistance, Ufd2 might play a role in cisplatin induced apoptosis. Our screening also highlighted the importance of the b7 subunit of 20S proteasome, whose corresponding human ortholog gene is PSMB4. Since PSMB4 is implicated in proteasomal degradation of SNEV, the absence of PSMB4 may pro duce resistance as a consequence of increased survival favoured by SNEV. To the best of our knowledge, none of the budding yeast homologues of the fission yeast mutants described in the present study has been previously linked to cis platin response. When we compared the present screening results with those obtained in previous global gene expression study, the importance of Lub1 emerged.

Indeed, the corre sponding budding yeast ortholog gene has a precise and important role in DNA damage response and appears to regulate the ubiquitination of both PCNA and histone H2B, through the interaction with UBC13 and UBP10. PCNA is at the very heart of many essential cellular processes, such as DNA replication, repair of DNA damage, chromatin structure maintenance, chro mosome segregation and cell cycle progression. This puts PCNA in a central position in determining the fate of replication fork, which ultimately determines both tumor progression as well as the outcome of anticancer treatment. In addition, recent advances have defined a clear role for histone H2B ubiquitination in transcriptional regulation and the enzymes regulating this post translational modification have been linked to tumorigenesis.

In summary, we can conclude that the cell sensitivity screening shown in the present study, together with evi dences resulting from previous S. pombe gene expres sion analysis, uncover novel putative targets for modulation of cisplatin sensitivity, particularly intriguing towards the discovery of strategies to overcome cisplatin in human tumors. Methods S. pombedeletion library A genome wide deletion Dacomitinib mutant library was constructed in large scale by PCR based targeted mutagenesis at each target ORF, on the base of the S.