Glycyrrhizic acid enhances the anticancer activity of cisplatin in the human ovarian cancer cell line.
Humans
Female
Cisplatin
/ pharmacology
Ovarian Neoplasms
/ drug therapy
Matrix Metalloproteinase 2
/ genetics
Matrix Metalloproteinase 9
/ genetics
Glycyrrhizic Acid
/ pharmacology
Cell Line, Tumor
Drug Resistance, Neoplasm
Apoptosis
Superoxide Dismutase
/ genetics
Antineoplastic Agents
/ pharmacology
Cell Proliferation
Chemotherapy
Cisplatin
Combination treatment
Glycyrrhizic acid
Ovarian cancer
Journal
Toxicology in vitro : an international journal published in association with BIBRA
ISSN: 1879-3177
Titre abrégé: Toxicol In Vitro
Pays: England
ID NLM: 8712158
Informations de publication
Date de publication:
Dec 2023
Dec 2023
Historique:
received:
28
04
2023
revised:
10
08
2023
accepted:
30
08
2023
medline:
23
10
2023
pubmed:
3
9
2023
entrez:
2
9
2023
Statut:
ppublish
Résumé
This study aimed to investigate the effects of glycyrrhizic acid (GL) on the anticancer activity of cisplatin in A2780 ovarian cancer cells. Cultured A2780 cells were treated with different concentrations of GL and cisplatin individually and in combination. The MTT assay, flow cytometry, wound-healing, and clonogenic assay, were used to determine cell viability, apoptosis, migration, and colony formation, respectively. The effects on superoxide dismutase (SOD) activity were also evaluated. QPCR was used to study the effects of individual and combined treatments with GL and cisplatin on the expression levels of migration genes (MMP2 and MMP9), and some apoptosis pathway genes (caspase-3, -8, -9, and BCL2). A synergistic effect was observed between GL and cisplatin (CI < 1). Combination therapy was significantly more effective in reducing cell viability, suppressing migration and colony formation, inducing apoptosis, and altering gene expression compared to single therapies. GL significantly increased SOD activity. The relative expression of caspase -3, -8, and - 9 increased significantly, and the expression levels of MMP2 and MMP9 decreased significantly in the treated cells. Our results indicate that GL enhances the anticancer activity of cisplatin in the A2780 cell line. Therefore, the combination of GL and cisplatin can be proposed as a promising therapeutic strategy for ovarian cancer.
Identifiants
pubmed: 37659683
pii: S0887-2333(23)00136-4
doi: 10.1016/j.tiv.2023.105687
pii:
doi:
Substances chimiques
Cisplatin
Q20Q21Q62J
Matrix Metalloproteinase 2
EC 3.4.24.24
Matrix Metalloproteinase 9
EC 3.4.24.35
Glycyrrhizic Acid
6FO62043WK
Superoxide Dismutase
EC 1.15.1.1
Antineoplastic Agents
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
105687Informations de copyright
Copyright © 2023 Elsevier Ltd. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.