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@article{2417662,
author = {Liskova, Veronika and Chovancova, Barbora and Galvankova, Kristina and Klena, Ladislav and Matyasova, Katarina and Babula, Petr and Grman, Marian and Rezuchova, Ingeborg and Bartosova, Maria and Križanová, Oľga},
article_location = {Basel},
article_number = {6},
doi = {http://dx.doi.org/10.3390/biom14060651},
keywords = {paclitaxel; breast cancer cell lines; apoptosis; slow sulfide donor; metabolism},
language = {eng},
issn = {2218-273X},
journal = {Biomolecules},
title = {Slow Sulfide Donor GYY4137 Increased the Sensitivity of Two Breast Cancer Cell Lines to Paclitaxel by Different Mechanisms},
url = {https://www.mdpi.com/2218-273X/14/6/651},
volume = {14},
year = {2024}
}
TY - JOUR
ID - 2417662
AU - Liskova, Veronika - Chovancova, Barbora - Galvankova, Kristina - Klena, Ladislav - Matyasova, Katarina - Babula, Petr - Grman, Marian - Rezuchova, Ingeborg - Bartosova, Maria - Križanová, Oľga
PY - 2024
TI - Slow Sulfide Donor GYY4137 Increased the Sensitivity of Two Breast Cancer Cell Lines to Paclitaxel by Different Mechanisms
JF - Biomolecules
VL - 14
IS - 6
SP - 1-17
EP - 1-17
PB - MDPI
SN - 2218273X
KW - paclitaxel
KW - breast cancer cell lines
KW - apoptosis
KW - slow sulfide donor
KW - metabolism
UR - https://www.mdpi.com/2218-273X/14/6/651
N2 - Paclitaxel (PTX) is a chemotherapeutic agent affecting microtubule polymerization. The efficacy of PTX depends on the type of tumor, and its improvement would be beneficial in patients' treatment. Therefore, we tested the effect of slow sulfide donor GYY4137 on paclitaxel sensitivity in two different breast cancer cell lines, MDA-MB-231, derived from a triple negative cell line, and JIMT1, which overexpresses HER2 and is resistant to trastuzumab. In JIMT1 and MDA-MB-231 cells, we compared IC50 and some metabolic (apoptosis induction, lactate/pyruvate conversion, production of reactive oxygen species, etc.), morphologic (changes in cytoskeleton), and functional (migration, angiogenesis) parameters for PTX and PTX/GYY4137, aiming to determine the mechanism of the sensitization of PTX. We observed improved sensitivity to paclitaxel in the presence of GYY4137 in both cell lines, but also some differences in apoptosis induction and pyruvate/lactate conversion between these cells. In MDA-MB-231 cells, GYY4137 increased apoptosis without affecting the IP3R1 protein, changing the morphology of the cytoskeleton. A mechanism of PTX sensitization by GYY4137 in JIMT1 cells is distinct from MDA-MB-231, and remains to be further elucidated. We suggest different mechanisms of action for H2S on the paclitaxel treatment of MDA-MB-231 and JIMT1 breast cancer cell lines.
ER -
LISKOVA, Veronika, Barbora CHOVANCOVA, Kristina GALVANKOVA, Ladislav KLENA, Katarina MATYASOVA, Petr BABULA, Marian GRMAN, Ingeborg REZUCHOVA, Maria BARTOSOVA a Oľga KRIŽANOVÁ. Slow Sulfide Donor GYY4137 Increased the Sensitivity of Two Breast Cancer Cell Lines to Paclitaxel by Different Mechanisms. \textit{Biomolecules}. Basel: MDPI, 2024, roč.~14, č.~6, s.~1-17. ISSN~2218-273X. Dostupné z: https://dx.doi.org/10.3390/biom14060651.
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