J 2024

Slow Sulfide Donor GYY4137 Increased the Sensitivity of Two Breast Cancer Cell Lines to Paclitaxel by Different Mechanisms

LISKOVA, Veronika, Barbora CHOVANCOVA, Kristina GALVANKOVA, Ladislav KLENA, Katarina MATYASOVA et. al.

Základní údaje

Originální název

Slow Sulfide Donor GYY4137 Increased the Sensitivity of Two Breast Cancer Cell Lines to Paclitaxel by Different Mechanisms

Autoři

LISKOVA, Veronika, Barbora CHOVANCOVA, Kristina GALVANKOVA, Ladislav KLENA, Katarina MATYASOVA, Petr BABULA (203 Česká republika, domácí), Marian GRMAN, Ingeborg REZUCHOVA, Maria BARTOSOVA a Oľga KRIŽANOVÁ (703 Slovensko, domácí)

Vydání

Biomolecules, Basel, MDPI, 2024, 2218-273X

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

10608 Biochemistry and molecular biology

Stát vydavatele

Švýcarsko

Utajení

není předmětem státního či obchodního tajemství

Odkazy

Impakt faktor

Impact factor: 5.500 v roce 2022

Organizační jednotka

Lékařská fakulta

UT WoS

001254538200001

Klíčová slova anglicky

paclitaxel; breast cancer cell lines; apoptosis; slow sulfide donor; metabolism

Štítky

Příznaky

Mezinárodní význam, Recenzováno
Změněno: 19. 8. 2024 10:31, Mgr. Tereza Miškechová

Anotace

V originále

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.