Overexpression of Glyoxalase 2 in Human Breast Cancer Cells: Implications for Cell Proliferation and Doxorubicin Resistance.
Humans
Doxorubicin
/ pharmacology
Drug Resistance, Neoplasm
/ genetics
Cell Proliferation
/ drug effects
Breast Neoplasms
/ metabolism
Female
Lactoylglutathione Lyase
/ metabolism
MCF-7 Cells
Cell Line, Tumor
Gene Expression Regulation, Neoplastic
/ drug effects
Protein Processing, Post-Translational
Oxidative Stress
/ drug effects
Cell Cycle
/ drug effects
Thiolester Hydrolases
S-glutathionylation
breast cancer cells
glyoxalase 2 (Glo2)
nucleus
proliferation
redox metabolism
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
10 Oct 2024
10 Oct 2024
Historique:
received:
18
07
2024
revised:
02
10
2024
accepted:
07
10
2024
medline:
26
10
2024
pubmed:
26
10
2024
entrez:
26
10
2024
Statut:
epublish
Résumé
Glyoxalase 2 (Glo2) is an enzyme of the glyoxalase system whose pathway parallels glycolysis and which aims to remove methylglyoxal (MGO). This study analyzed the possible additional roles of the Glo2 enzyme in breast cancer (MCF7) and non-cancer (HDF) cell lines, investigating its presence at the nuclear level and its potential involvement in cell proliferation and chemotherapy resistance. The results revealed that Glo2 is overexpressed in cancer cells, and its expression is higher during the proliferative (S and G2/M) phases of the cell cycle. The study also examined a post-translational modification (PTM) in which Glo2 could be involved, with S-glutathionylation revealing that Glo2 enhances this PTM in cancer cells both in the cytoplasm and nucleus. Inhibition of Glo2 by p-NCBG resulted in increased sensitivity to doxorubicin, a common chemotherapeutic agent. This suggests that Glo2 increases cancer cell resistance to chemotherapy, potentially through its role in regulating oxidative stress. These results highlight Glo2 as a potential therapeutic target to improve the efficacy of existing treatments.
Identifiants
pubmed: 39456676
pii: ijms252010888
doi: 10.3390/ijms252010888
pii:
doi:
Substances chimiques
Doxorubicin
80168379AG
Lactoylglutathione Lyase
EC 4.4.1.5
hydroxyacylglutathione hydrolase
EC 3.1.2.6
Thiolester Hydrolases
EC 3.1.2.-
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM