Results 21 to 30 of about 1,442,074 (300)

Proteasome inhibitors block DNA repair and radiosensitize non-small cell lung cancer. [PDF]

open access: yesPLoS ONE, 2013
Despite optimal radiation therapy (RT), chemotherapy and/or surgery, a majority of patients with locally advanced non-small cell lung cancer (NSCLC) fail treatment. To identify novel gene targets for improved tumor control, we performed whole genome RNAi
Kyle R Cron   +8 more
doaj   +1 more source

Assembly of the Drosophila 26 S proteasome is accompanied by extensive subunit rearrangements [PDF]

open access: yes, 2002
The subunit contacts in the regulatory complex of the Drosophila 26 S proteasome were studied through the cross-linking of closely spaced subunits of the complex, and analysis of the cross-linking pattern in an immunoblot assay with the use of subunit ...
Kapelari, Barbara   +13 more
core   +2 more sources

Inhibition of proteasomal degradation of rpn4 impairs nonhomologous end-joining repair of DNA double-strand breaks. [PDF]

open access: yesPLoS ONE, 2010
BACKGROUND: The proteasome homeostasis in Saccharomyces cerevisiae is regulated by a negative feedback circuit in which the transcription factor Rpn4 induces the proteasome genes and is rapidly degraded by the assembled proteasome.
Donghong Ju   +4 more
doaj   +1 more source

Dss1 Is a 26S Proteasome Ubiquitin Receptor [PDF]

open access: yes, 2014
The ubiquitin-proteasome system is the major pathway for protein degradation in eukaryotic cells. Proteins to be degraded are conjugated to ubiquitin chains that act as recognition signals for the 26S proteasome.
Hardwick, Kevin G.   +20 more
core   +1 more source

Bortezomib Amplifies Effect on Intracellular Proteasomes by Changing Proteasome Structure

open access: yesEBioMedicine, 2015
The proteasome inhibitor Bortezomib is used to treat multiple myeloma (MM). Bortezomib inhibits protein degradation by inactivating proteasomes' active-sites. MM cells are exquisitely sensitive to Bortezomib – exhibiting a low-nanomolar IC50 – suggesting
David S. Pitcher   +5 more
doaj   +1 more source

Experimental and computational analysis of polyglutamine-mediated cytotoxicity. [PDF]

open access: yesPLoS Computational Biology, 2010
Expanded polyglutamine (polyQ) proteins are known to be the causative agents of a number of human neurodegenerative diseases but the molecular basis of their cytoxicity is still poorly understood.
Matthew Y Tang   +3 more
doaj   +1 more source

Proteasome inhibition induces IKK-dependent interleukin-8 expression in triple negative breast cancer cells: Opportunity for combination therapy. [PDF]

open access: yesPLoS ONE, 2018
Triple negative breast cancer (TNBC) cells express increased levels of the pro-inflammatory and pro-angiogenic chemokine interleukin-8 (IL-8, CXCL8), which promotes their proliferation and migration.
Mohammad M Uddin   +4 more
doaj   +1 more source

Immunoproteasome Activity and Content Determine Hematopoietic Cell Sensitivity to ONX-0914 and to the Infection of Cells with Lentiviruses

open access: yesCells, 2021
Proteasomes are intracellular structures responsible for protein degradation. The 20S proteasome is a core catalytic element of the proteasome assembly.
Elmira Vagapova   +8 more
doaj   +1 more source

Proteasome inhibition in hematologic malignancies

open access: yesAnnals of Medicine, 2004
Hematologic malignancies, including multiple myeloma (MM), will account for more than 100,000 new cases of cancer and over 57,000 deaths in the United States in 2003. Treatment of MM is a serious challenge, because despite a variety of available therapies, median survival is short.
Paul G, Richardson   +3 more
openaire   +2 more sources

Evaluation of the NRF1-proteasome axis as a therapeutic target in breast cancer

open access: yesScientific Reports, 2023
Proteasomes are multi-subunit complexes that specialize in protein degradation. Cancer cells exhibit a heightened dependence on proteasome activity, presumably to support their enhanced proliferation and other cancer-related characteristics.
Holly A. Byers   +7 more
doaj   +1 more source

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