Antigen selection in B-cell lymphomas-Tracing the evidence
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14740%2F13%3A00072727" target="_blank" >RIV/00216224:14740/13:00072727 - isvavai.cz</a>
Result on the web
<a href="http://ac.els-cdn.com/S1044579X1300076X/1-s2.0-S1044579X1300076X-main.pdf?_tid=53d1b2dc-bfba-11e3-91ac-00000aab0f6b&acdnat=1397029454_a5ad89568b55191984c5a6ad89549a75" target="_blank" >http://ac.els-cdn.com/S1044579X1300076X/1-s2.0-S1044579X1300076X-main.pdf?_tid=53d1b2dc-bfba-11e3-91ac-00000aab0f6b&acdnat=1397029454_a5ad89568b55191984c5a6ad89549a75</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.semcancer.2013.07.006" target="_blank" >10.1016/j.semcancer.2013.07.006</a>
Alternative languages
Result language
angličtina
Original language name
Antigen selection in B-cell lymphomas-Tracing the evidence
Original language description
While signaling through the B cell receptor (BcR) facilitates B cell development and maintenance, it also carries intertwined risks for the development of lymphomas since malignant B cells can exploit these pathways in order to trigger and fuel clonal expansion. This corruption of the normal B cell response to antigens, leading to sustained BcR signaling, has given great impulse to investigate in detail the role of antigen in lymphomas. Suffice it to conclude from such studies, largely immunogenetics based, that the evidence implicating antigens (exogenous or self) in lymphoma development is substantial and that lymphomagenesis is functionally driven and dynamic, rather than a simple stochastic process. As the paradigm of antigen-driven lymphoma evolves, further investigation will be paramount to the identification of the inciting agent(s) that may be responsible for immunoproliferative neoplasms and also for the development of therapeutic agents targeting effectors of the BcR signalin
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
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Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2013
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Seminars in Cancer Biology
ISSN
1044-579X
e-ISSN
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Volume of the periodical
23
Issue of the periodical within the volume
6
Country of publishing house
GB - UNITED KINGDOM
Number of pages
11
Pages from-to
399-409
UT code for WoS article
000329011000002
EID of the result in the Scopus database
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