Cytosolic and mitochondrial ROS production resulted in apoptosis induction in breast cancer cells treated with Crocin: The role of FOXO3a, PTEN and AKT signaling.
Acetylcysteine
/ pharmacology
Antineoplastic Agents
/ pharmacology
Apoptosis
/ drug effects
Bcl-2-Like Protein 11
/ genetics
Carotenoids
/ pharmacology
Caspase 3
/ genetics
Cell Line, Tumor
Cell Survival
/ drug effects
Cytosol
/ drug effects
Forkhead Box Protein O3
/ agonists
Gene Expression Regulation, Neoplastic
Humans
MCF-7 Cells
Mitochondria
/ drug effects
Onium Compounds
/ pharmacology
PTEN Phosphohydrolase
/ genetics
Poly(ADP-ribose) Polymerases
/ genetics
Proto-Oncogene Proteins c-akt
/ antagonists & inhibitors
Proto-Oncogene Proteins c-bcl-2
/ genetics
Reactive Oxygen Species
/ agonists
Signal Transduction
bcl-2-Associated X Protein
/ genetics
AKT survival pathway
Cytosolic ROS
FOXO3a
Mitochondrial damage
PTEN
Journal
Biochemical pharmacology
ISSN: 1873-2968
Titre abrégé: Biochem Pharmacol
Pays: England
ID NLM: 0101032
Informations de publication
Date de publication:
07 2020
07 2020
Historique:
received:
01
12
2019
accepted:
24
04
2020
pubmed:
1
5
2020
medline:
2
12
2020
entrez:
1
5
2020
Statut:
ppublish
Résumé
Different groups have reported the Crocin anticancer activity. We previously showed Crocin-induced apoptosis in rat model of breast and gastric cancers, through the increased Bax/Bcl-2 ratio and caspases activity, as well as the cell cycle arrest in a p53-dependent manner. Since Crocin antioxidant activity has been shown under different conditions, it is interesting to elucidate its apoptotic mechanism. Here, we treated two breast cancer cell lines, MCF-7 and MDA-MB-231, with Crocin. MTT and ROS assays, cell cycle arrest, Bax/Bcl-2 ratio and caspase3 activity were determined. PARP cleavage and expression of some proteins were studied using Western blotting and immunofluorescence. The results indicated stepwise ROS generation in cytosol and mitochondria after Crocin treatment. Attenuating the early ROS level, using diphenyleneiodonium, diminished the sequent mitochondrial damage (decreasing Δψ) and downstream apoptotic signaling. Crocin induced ROS production, FOXO3a expression and nuclear translocation, and then, elevation of the expression of FOXO3a target genes (Bim and PTEN) and caspase-3 activation. Application of N-acetylcysteine blocked AKT/FOXO3a/Bim signaling. FOXO3a knockdown resulted in a decrease of Bim, PTEN and caspase 3, after Crocin treatment. PTEN knockdown caused a decrease in FOXO3a, Bim and caspase 3, in addition to an increase in p-AKT and p-FOXO3a, after Crocin treatment. In conclusion, Crocin induced apoptosis in MCF-7 and MDA-MB-231 human breast cancer cells. The ROS-activated FOXO3a cascade plays a central role in this process. FOXO3a-mediated upregulation of PTEN exerted a further inhibition of the AKT survival pathway. These data provide a new insight into applications of Crocin for cancer therapy.
Identifiants
pubmed: 32353423
pii: S0006-2952(20)30227-6
doi: 10.1016/j.bcp.2020.113999
pii:
doi:
Substances chimiques
Antineoplastic Agents
0
BAX protein, human
0
BCL2 protein, human
0
Bcl-2-Like Protein 11
0
FOXO3 protein, human
0
Forkhead Box Protein O3
0
Onium Compounds
0
Proto-Oncogene Proteins c-bcl-2
0
Reactive Oxygen Species
0
bcl-2-Associated X Protein
0
Carotenoids
36-88-4
diphenyleneiodonium
6HJ411TU98
crocin
877GWI46C2
Poly(ADP-ribose) Polymerases
EC 2.4.2.30
Proto-Oncogene Proteins c-akt
EC 2.7.11.1
PTEN Phosphohydrolase
EC 3.1.3.67
PTEN protein, human
EC 3.1.3.67
CASP3 protein, human
EC 3.4.22.-
Caspase 3
EC 3.4.22.-
Acetylcysteine
WYQ7N0BPYC
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
113999Informations de copyright
Copyright © 2020. Published by Elsevier Inc.
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.