The development of proteasome inhibitors as anticancer drugs.
By J. Adams. Cancer Cell, 2004
788 citations recorded by the source corpus.
Subfields: Hematology, Molecular Biology, Oncology
View Paper: https://www.semanticscholar.org/paper/9b906348aac7416ead8fecc9816f345ec784e3fd
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Citations in the corpus
- Building ubiquitin chains: E2 enzymes at work (2009, background): “Such drugs might join the proteasome inhibitor Velcade (also known as Bortezomib”
- Mechanisms of Disease: oncogene addiction—a rationale for molecular targeting in cancer therapy (2006, background): “Conversely, inhibitors of the proteosome-ubiquination proteolysis pathway such as bortezomi”
- Targeting the ubiquitin system in cancer therapy (2009, background): “Bortezomib downregulates NF-κB signalling by blocking IκB degradation, which seems to be its prevalent mechanism of action in human tumour”
- The role of the unfolded protein response in tumour development: friend or foe? (2004, neutral): “Proteasome inhibitors are being used to successfully treat patients with multiple myelom”
- Autophagy as a target for anticancer therapy (2011, background): “Inhibitors of mTORC1 Specific chemical inhibitors of the proteasome have emerged as effective antitumor therapies”