Flow cytometric monitoring of the in vitro inhibition of the phosphorylation of CRKL and of SRC family kinases in patients with chronic myelogenous leukemia treated with tyrosine kinase inhibitors
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15110%2F15%3A33150317" target="_blank" >RIV/61989592:15110/15:33150317 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/00098892:_____/15:#0000904
Výsledek na webu
<a href="http://dx.doi.org/10.1111/ijlh.12258" target="_blank" >http://dx.doi.org/10.1111/ijlh.12258</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1111/ijlh.12258" target="_blank" >10.1111/ijlh.12258</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Flow cytometric monitoring of the in vitro inhibition of the phosphorylation of CRKL and of SRC family kinases in patients with chronic myelogenous leukemia treated with tyrosine kinase inhibitors
Popis výsledku v původním jazyce
Sir, Monitoring BCR-ABL1 kinase activity by assaying CRKL phosphorylation (P-CRKL), a technique first introduced by Gorre et al, has proven to be a reliable method for the assessment of the sensitivity and/or resistance of leukemia cells from CML patients to tyrosine kinase inhibitors (TKIs) . In BCR-ABL1-positive cells, P-CRKL is inhibited by TKIs, including imatinib (IM), dasatinib (DAS) and nilotinib (NIL), in a dose-dependent manner. Originally, Western blotting with anti-CRKL antibody was used by several laboratories, including our own, to detect the change in phosphorylation of CRKL. These assays usually involve in vitro analyses of mononuclear cells in which the status of BCR-ABL1 kinase inhibition induced by TKI is measured, or in vivo analysesusing freshly drawn samples. A predictive value was established for the extent of inhibition (e.g., for 50% reduction) of P-CRKL from baseline during a defined time interval of treatment. Later, a flow cytometry method to measure in vivo
Název v anglickém jazyce
Flow cytometric monitoring of the in vitro inhibition of the phosphorylation of CRKL and of SRC family kinases in patients with chronic myelogenous leukemia treated with tyrosine kinase inhibitors
Popis výsledku anglicky
Sir, Monitoring BCR-ABL1 kinase activity by assaying CRKL phosphorylation (P-CRKL), a technique first introduced by Gorre et al, has proven to be a reliable method for the assessment of the sensitivity and/or resistance of leukemia cells from CML patients to tyrosine kinase inhibitors (TKIs) . In BCR-ABL1-positive cells, P-CRKL is inhibited by TKIs, including imatinib (IM), dasatinib (DAS) and nilotinib (NIL), in a dose-dependent manner. Originally, Western blotting with anti-CRKL antibody was used by several laboratories, including our own, to detect the change in phosphorylation of CRKL. These assays usually involve in vitro analyses of mononuclear cells in which the status of BCR-ABL1 kinase inhibition induced by TKI is measured, or in vivo analysesusing freshly drawn samples. A predictive value was established for the extent of inhibition (e.g., for 50% reduction) of P-CRKL from baseline during a defined time interval of treatment. Later, a flow cytometry method to measure in vivo
Klasifikace
Druh
J<sub>x</sub> - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
CEP obor
FD - Onkologie a hematologie
OECD FORD obor
—
Návaznosti výsledku
Projekt
<a href="/cs/project/NT12218" target="_blank" >NT12218: Individualizovaná léčba chronických myeloproliferativních stavů a myelodysplastického syndromu - studie buněčné metabolomiky</a><br>
Návaznosti
S - Specificky vyzkum na vysokych skolach
Ostatní
Rok uplatnění
2015
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
International Journal of Laboratory Hematology
ISSN
1751-553X
e-ISSN
—
Svazek periodika
37
Číslo periodika v rámci svazku
1
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
5
Strana od-do
"e11"-"e15"
Kód UT WoS článku
—
EID výsledku v databázi Scopus
—