The proteasome inhibitor PS-341 potentiates sensitivity of multiple myeloma cells to conventional chemotherapeutic agents: therapeutic applications.
By N. Mitsiades, C. Mitsiades, P. Richardson, V. Poulaki, Y. Tai, D. Chauhan, G. Fanourakis, Xuesong Gu, Charles Bailey, Marie G. Joseph and 5 more. Blood, 2003
747 citations recorded by the source corpus.
Subfields: Molecular Biology, Oncology
View Paper: https://www.semanticscholar.org/paper/b14df5fb59dcd99cbe4972f8fa68033b17f6850b
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In Molecular Biology
In Oncology
Citations in the corpus
- Anthracyclines: Molecular Advances and Pharmacologic Developments in Antitumor Activity and Cardiotoxicity (2004, background): “proteasome inhibitor PS-341 sensitized multiple myeloma cell lines and patient cells to DOX, including cells resistant to either drug or cells isolated from a patient who had relapsed after proteasome inhibitor monotherapy (Mitsiades et al., 2003).”
- Is NF-κB a good target for cancer therapy? Hopes and pitfalls (2009, background): “Although bortezomib affects other signalling pathways, its efficacy may in part be due to inhibition of NF-κB activit”
- Understanding multiple myeloma pathogenesis in the bone marrow to identify new therapeutic targets (2007, background): “For example, gene and protein profiling of bortezomib-treated multiple myeloma cells shows cleavage of DNA repair enzyme”
- The proteasome: a suitable antineoplastic target (2004, positive): “Others have shown that low-dose bortezomib sensitizes chemotherapy-resistant multiple-myeloma cells and cells obtained from a patient with relapsed disease to chemotherapy with doxorubicin and melphala”