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The proteasomeinhibitor bortezomib is an efficacious apoptotic agent in many tumor cells.
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Bortezomib is the first proteasomeinhibitor drug tested in human patients.
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However, a significant proportion of patients who receive a proteasomeinhibitor-containing regime show cardiotoxicity.
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Therefore, the proteasomeinhibitor MG132 should be further evaluated for combination therapy with TRAIL.
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The introduction of proteasomeinhibitor and immunomodulatory drugs has considerably changed the treatment paradigm of multiple myeloma.
Usage of proteasome inhibitors in English
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That system is a target for anticancer strategies by using proteasomeinhibitors.
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Nevertheless, the mechanisms of apoptosis induced by proteasomeinhibitors remain unclear.
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Both Kyprolis and Velcade are members of a class known as proteasomeinhibitors.
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Overall, these findings suggest proteasomeinhibitors as potential latency reversing agents.
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Overall, we determined the unique and novel mechanism of FOXM1 suppression by proteasomeinhibitors.
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Identification of capzimin offers an alternative path to develop proteasomeinhibitors for cancer therapy.
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We identified proteasomeinhibitors as the first type of drugs that target FOXM1 in cancer cells.
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This suggests that proteasomeinhibitors could also be used for rapidly reducing autoantibody production in autoimmune diseases.
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Overcoming resistance of tumor cells to anticancer agents, such as proteasomeinhibitors, could improve their clinical efficacy.
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These results indicate that p53 downstream targets can collectively modulate apoptotic response to bortezomib and other proteasomeinhibitors.
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The introduction of newer proteasomeinhibitors with activity in bortezomib-resistant disease and reduced toxicity profiles may yield further benefits.
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This was confirmed by the lack of inhibition of IAV entry by proteasomeinhibitors in a virus-like particle fusion assay.
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Pretreatment of DC with proteasomeinhibitors strongly enhanced the immunogenicity of single viral synthetic as well as bulk LCL peptides.
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This screen identified 100 genes whose knockdown affected lethality to bortezomib and to a structurally diverse set of other proteasomeinhibitors.
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The use of proteasomeinhibitors to target cancer's dependence on altered protein homeostasis has been greatly limited by intrinsic a …
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Moreover, proteasomeinhibitors reduced receptor internalization and degradation, thus implicating a role for the ubiquitination machinery in the trafficking of the beta2AR.