Proteasome inhibitors - molecular basis and current perspectives in multiple myeloma
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14110%2F14%3A00075479" target="_blank" >RIV/00216224:14110/14:00075479 - isvavai.cz</a>
Alternative codes found
RIV/61988987:17110/14:A1501CGD RIV/65269705:_____/14:00061495 RIV/00843989:_____/14:E0104311
Result on the web
<a href="http://dx.doi.org/10.1111/jcmm.12279" target="_blank" >http://dx.doi.org/10.1111/jcmm.12279</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1111/jcmm.12279" target="_blank" >10.1111/jcmm.12279</a>
Alternative languages
Result language
angličtina
Original language name
Proteasome inhibitors - molecular basis and current perspectives in multiple myeloma
Original language description
Inhibition of proteasome, a proteolytic complex responsible for the degradation of ubiquitinated proteins, has emerged as a powerful strategy for treatment of multiple myeloma (MM), a plasma cell malignancy. First-in-class agent, bortezomib, has demonstrated great positive therapeutic efficacy in MM, both in pre-clinical and in clinical studies. However, despite its high efficiency, a large proportion of patients do not achieve sufficient clinical response. Therefore, the development of a second-generation of proteasome inhibitors (PIs) with improved pharmacological properties was needed. Recently, several of these new agents have been introduced into clinics including carfilzomib, marizomib and ixazomib. Further, new orally administered second-generation PI oprozomib is being investigated. This review provides an overview of main mechanisms of action of PIs in MM, focusing on the ongoing development and progress of novel anti-proteasome therapeutics.
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
FD - Oncology and haematology
OECD FORD branch
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Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>Z - Vyzkumny zamer (s odkazem do CEZ)
Others
Publication year
2014
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Journal of Cellular and Molecular Medicine
ISSN
1582-4934
e-ISSN
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Volume of the periodical
18
Issue of the periodical within the volume
6
Country of publishing house
US - UNITED STATES
Number of pages
15
Pages from-to
947-961
UT code for WoS article
000340390500001
EID of the result in the Scopus database
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