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EP4 receptor agonist L-902688 augments cytotoxic activities of ibrutinib, idelalisib, and venetoclax against chronic lymphocytic leukemia cells
ID
Nabergoj, Sanja
(
Author
),
ID
Markovič, Tijana
(
Author
),
ID
Avsec, Damjan
(
Author
),
ID
Gobec, Martina
(
Author
),
ID
Podgornik, Helena
(
Author
),
ID
Jakopin, Žiga
(
Author
),
ID
Mlinarič-Raščan, Irena
(
Author
)
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https://www.sciencedirect.com/science/article/pii/S0006295220305888
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Abstract
Treatment of patients with relapsed or refractory chronic lymphocytic leukemia (CLL) has significantly improved more recently with the approval of several new agents, including ibrutinib, idelalisib, and venetoclax. Despite the outstanding efficacies observed with these agents, these treatments are sometimes discontinued due to toxicity, unresponsiveness, transformation of the disease and/or resistance. Constitutive NF-κB activation that protects CLL cells from apoptotic stimuli represents one of molecular mechanisms that underlie the emergence of drug resistance. As prostaglandin E (EP)4 receptor agonists have been shown to successfully inhibit the NF-κB pathway in B-cell lymphoma cells, we investigated the potential of the highly specific EP4 receptor agonist L-902688 for the potential treatment of patients with CLL. We show here that low micromolar concentrations of L-902688 can indeed induce selective cytotoxicity towards several B-cell malignancies, including CLL. Moreover, L-902688-mediated activation of the EP4 receptor in patient derived CLL cells resulted in inhibition of the NF-κB pathway, cell proliferation, and induction of apoptosis. Most importantly, we show for the first time that in combination with ibrutinib, idelalisib, or venetoclax, L-902688 induces synergistic cytotoxic activity against patient derived CLL cells. To conclude, the modulation of NF-κB activity by EP4 receptor agonists represents an innovative approach to improve the treatment of patients with CLL. In particular, EP4 receptor agonists appear to represent promising adjuncts to the already existing therapies for patients with CLL due to these promising synergistic activities.
Language:
English
Keywords:
chronic lymphocytic leukemia
,
L-902688
,
NF-κB inhibition
,
prostaglandin E4
,
receptor
,
synergistic cytotoxic activity
,
prostaglandin E4 receptor
Work type:
Article
Typology:
1.01 - Original Scientific Article
Organization:
FFA - Faculty of Pharmacy
Publication status:
Published
Publication version:
Version of Record
Year:
2021
Number of pages:
14 str.
Numbering:
Vol. 183, art. 114352
PID:
20.500.12556/RUL-138397
UDC:
616.155.392+577.27
ISSN on article:
0006-2952
DOI:
10.1016/j.bcp.2020.114352
COBISS.SI-ID:
43415299
Publication date in RUL:
19.07.2022
Views:
2300
Downloads:
130
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Record is a part of a journal
Title:
Biochemical pharmacology
Shortened title:
Biochem. pharmacol.
Publisher:
Elsevier
ISSN:
0006-2952
COBISS.SI-ID:
276759
Licences
License:
CC BY-NC-ND 4.0, Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
Link:
http://creativecommons.org/licenses/by-nc-nd/4.0/
Description:
The most restrictive Creative Commons license. This only allows people to download and share the work for no commercial gain and for no other purposes.
Secondary language
Language:
Slovenian
Keywords:
prostaglandin E4
,
receptorji
,
sinergistična citotoksična aktivnost
,
celice kronične limfocitne levkemije
,
kronična limfocitna levkemija
,
citotoksičnost
Projects
Funder:
ARRS - Slovenian Research Agency
Project number:
P1-0208
Name:
Farmacevtska kemija: načrtovanje, sinteza in vrednotenje učinkovin
Funder:
ARRS - Slovenian Research Agency
Project number:
NC-0004
Name:
NOBIL - Novi biološki označevalci v levkemiji
Funder:
EC - European Commission
Funding programme:
European Regional Development Fund
Acronym:
EATRIS-TRI.SI
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