2020
PRIMA-1MET cytotoxic effect correlates with p53 protein reduction in TP53-mutated chronic lymphocytic leukemia cells
JAŠKOVÁ, Zuzana, Šárka PAVLOVÁ, Jitka MALČÍKOVÁ, Yvona BRYCHTOVÁ, Martin TRBUŠEK et. al.Základní údaje
Originální název
PRIMA-1MET cytotoxic effect correlates with p53 protein reduction in TP53-mutated chronic lymphocytic leukemia cells
Autoři
JAŠKOVÁ, Zuzana (703 Slovensko, domácí), Šárka PAVLOVÁ (203 Česká republika, domácí), Jitka MALČÍKOVÁ (203 Česká republika, domácí), Yvona BRYCHTOVÁ (203 Česká republika, domácí) a Martin TRBUŠEK (203 Česká republika, garant, domácí)
Vydání
Leukemia Research, Oxford, Pergamon Press, 2020, 0145-2126
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30205 Hematology
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 3.156
Kód RIV
RIV/00216224:14110/20:00115275
Organizační jednotka
Lékařská fakulta
UT WoS
000509785500002
Klíčová slova anglicky
Chronic lymphocytic leukemia; TP53/p53; PRIMA-1(MET); Apoptosis
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 9. 11. 2020 10:55, Mgr. Tereza Miškechová
Anotace
V originále
TP53 gene defects represent the most unfavorable prognostic factor in chronic lymphocytic leukemia (CLL). Although recently introduced small-molecule B-cell receptor signalling inhibitors have revolutionized CLL treatment, data for ibrutinib still point to impaired prognosis for TP53-affected patients. Among cancer-associated TP53 mutations, missense substitutions predominate and typically result in a high mutated-p53 protein level. Therefore, rescuing the p53 tumor suppressor function through specific small molecules restoring p53 wild-type (wt) conformation represents an attractive therapeutic strategy for cancer patients with TP53 missense mutations. We tested the effect of mutated-p53 reactivating molecule PRIMA-1(MET) in 62 clinical CLL samples characterized for TP53 mutations and p53 protein level. At the subtle PRIMA-1(MET) concentrations (1-4 mu M), most samples manifested concentration-dependent viability decrease and, conversely, apoptosis induction, with the response being similar in both the TP53-mutated and TP53-wt groups, as well as in the TP53-mutated samples with p53 protein stabilization and without it. PRIMA-1(MET) was able to reduce mutated p53 protein in a proportion of TP53-mutated CLL samples, and this reduction correlated with a significantly stronger viability decrease and apoptosis induction than samples with stable p53 levels. CLL cells are mostly sensitive to PRIMA-1(MET) apart from those with stable mutated p53.
Návaznosti
MUNI/A/1105/2018, interní kód MU |
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