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@article{53250,
   author = {Paukovčeková, Silvia and Krchniaková, Mária and Chlapek, Petr and Neradil, Jakub and Škoda, Jan and Veselská, Renata},
   article_location = {Basel},
   article_number = {15},
   doi = {http://dx.doi.org/10.3390/ijms23158549},
   keywords = {thiosemicarbazones; anthracyclines; anthracenedione; pediatric solid tumors; combined anticancer treatment; checkpoint kinase 1; double strand breaks in DNA},
   language = {eng},
   issn = {1661-6596},
   journal = {International Journal of Molecular Sciences},
   title = {Thiosemicarbazones Can Act Synergistically with Anthracyclines to Downregulate CHEK1 Expression and Induce DNA Damage in Cell Lines Derived from Pediatric Solid Tumors},
   url = {https://www.mdpi.com/1422-0067/23/15/8549},
   volume = {23},
   year = {2022}
}

TY  - JOUR
ID  - 53250
AU  - Paukovčeková, Silvia - Krchniaková, Mária - Chlapek, Petr - Neradil, Jakub - Škoda, Jan - Veselská, Renata
PY  - 2022
TI  - Thiosemicarbazones Can Act Synergistically with Anthracyclines to Downregulate CHEK1 Expression and Induce DNA Damage in Cell Lines Derived from Pediatric Solid Tumors
JF  - International Journal of Molecular Sciences
VL  - 23
IS  - 15
SP  - 1-19
EP  - 1-19
PB  - MDPI
SN  - 1661-6596
KW  - thiosemicarbazones
KW  - anthracyclines
KW  - anthracenedione
KW  - pediatric solid tumors
KW  - combined anticancer treatment
KW  - checkpoint kinase 1
KW  - double strand breaks in DNA
UR  - https://www.mdpi.com/1422-0067/23/15/8549
N2  - Anticancer therapy by anthracyclines often leads to the development of multidrug resistance (MDR), with subsequent treatment failure. Thiosemicarbazones have been previously suggested as suitable anthracycline partners due to their ability to overcome drug resistance through dual Pgp-dependent cytotoxicity-inducing effects. Here, we focused on combining anthracyclines (doxorubicin, daunorubicin, and mitoxantrone) and two thiosemicarbazones (DpC and Dp44mT) for treating cell types derived from the most frequent pediatric solid tumors. Our results showed synergistic effects for all combinations of treatments in all tested cell types. Nevertheless, further experiments revealed that this synergism was independent of Pgp expression but rather resulted from impaired DNA repair control leading to cell death via mitotic catastrophe. The downregulation of checkpoint kinase 1 (CHEK1) expression by thiosemicarbazones and the ability of both types of agents to induce double-strand breaks in DNA may explain the Pgp-independent synergism between anthracyclines and thiosemicarbazones. Moreover, the concomitant application of these agents was found to be the most efficient approach, achieving the strongest synergistic effect with lower concentrations of these drugs. Overall, our study identified a new mechanism that offers an avenue for combining thiosemicarbazones with anthracyclines to treat tumors regardless the Pgp status.
ER  - 

PAUKOVČEKOVÁ, Silvia, Mária KRCHNIAKOVÁ, Petr CHLAPEK, Jakub NERADIL, Jan ŠKODA a Renata VESELSKÁ. Thiosemicarbazones Can Act Synergistically with Anthracyclines to Downregulate CHEK1 Expression and Induce DNA Damage in Cell Lines Derived from Pediatric Solid Tumors. \textit{International Journal of Molecular Sciences}. Basel: MDPI, 2022, roč.~23, č.~15, s.~1-19. ISSN~1661-6596. Dostupné z: https://dx.doi.org/10.3390/ijms23158549.