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MLN2238, a proteasome inhibitor, induces caspase-dependent cell death, cell cycle arrest, and potentiates the cytotoxic activity of chemotherapy agents in rituximab-chemotherapy-sensitive or rituximab-chemotherapy-resistant B-cell lymphoma preclinical models

To further develop therapeutic strategies targeting the proteasome system, we studied the antitumor activity and mechanisms of action of MLN2238, a reversible proteasome inhibitor, in preclinical lymphoma models. Experiments were conducted in rituximab-chemotherapy-sensitive cell lines, rituximab-ch...

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Publicat a:Anticancer Drugs
Autors principals: Gu, Juan J., Hernandez-Ilizaliturri, Francisco J., Mavis, Cory, Czuczman, Natalie M., Deeb, George, Gibbs, John, Skitzki, Joseph J., Patil, Ritesh, Czuczman, Myron S.
Format: Artigo
Idioma:Inglês
Publicat: 2013
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5685502/
https://ncbi.nlm.nih.gov/pubmed/23995855
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/CAD.0000000000000008
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