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@article{2216037,
author = {Farsa, Oldřich and Ballayová, Veronika and Žáčková, Radka and Kollár, Peter and Kauerová, Tereza and Zubáč, Peter},
article_location = {Basel},
article_number = {17},
doi = {http://dx.doi.org/10.3390/ijms23179813},
keywords = {aminopeptidase N; acetamidophenones; Schiff bases; semicarbazones; thiosemicarbazones; inhibition of proliferation},
language = {eng},
issn = {1422-0067},
journal = {International Journal of Molecular Sciences},
title = {Aminopeptidase N Inhibitors as Pointers for Overcoming Antitumor Treatment Resistance},
url = {https://www.mdpi.com/1422-0067/23/17/9813/htm},
volume = {23},
year = {2022}
}
TY - JOUR
ID - 2216037
AU - Farsa, Oldřich - Ballayová, Veronika - Žáčková, Radka - Kollár, Peter - Kauerová, Tereza - Zubáč, Peter
PY - 2022
TI - Aminopeptidase N Inhibitors as Pointers for Overcoming Antitumor Treatment Resistance
JF - International Journal of Molecular Sciences
VL - 23
IS - 17
SP - 1-15
EP - 1-15
PB - Multidisciplinary Digital Publishing Institute
SN - 14220067
KW - aminopeptidase N
KW - acetamidophenones
KW - Schiff bases
KW - semicarbazones
KW - thiosemicarbazones
KW - inhibition of proliferation
UR - https://www.mdpi.com/1422-0067/23/17/9813/htm
N2 - Aminopeptidase N (APN), also known as CD13 antigen or membrane alanyl aminopeptidase, belongs to the M1 family of the MA clan of zinc metallopeptidases. In cancer cells, the inhibition of aminopeptidases including APN causes the phenomenon termed the amino acid deprivation response (AADR), a stress response characterized by the upregulation of amino acid transporters and synthetic enzymes and activation of stress-related pathways such as nuclear factor kB (NFkB) and other pro-apoptotic regulators, which leads to cancer cell death by apoptosis. Recently, APN inhibition has been shown to augment DR4-induced tumor cell death and thus overcome resistance to cancer treatment with DR4-ligand TRAIL, which is available as a recombinant soluble form dulanermin. This implies that APN inhibitors could serve as potential weapons for overcoming cancer treatment resistance. In this study, a series of basically substituted acetamidophenones and the semicarbazones and thiosemicarbazones derived from them were prepared, for which APN inhibitory activity was determined. In addition, a selective anti-proliferative activity against cancer cells expressing APN was demonstrated. Our semicarbazones and thiosemicarbazones are the first compounds of these structural types of Schiff bases that were reported to inhibit not only a zinc-dependent aminopeptidase of the M1 family but also a metalloenzyme.
ER -
FARSA, Oldřich, Veronika BALLAYOVÁ, Radka ŽÁČKOVÁ, Peter KOLLÁR, Tereza KAUEROVÁ a Peter ZUBÁČ. Aminopeptidase N Inhibitors as Pointers for Overcoming Antitumor Treatment Resistance. \textit{International Journal of Molecular Sciences}. Basel: Multidisciplinary Digital Publishing Institute, 2022, roč.~23, č.~17, s.~1-15. ISSN~1422-0067. Dostupné z: https://dx.doi.org/10.3390/ijms23179813.
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