Elucidating the anti-melanoma effect and mechanisms of Hispolon.
Animals
Antineoplastic Agents
/ administration & dosage
Apoptosis
/ drug effects
Catechols
/ administration & dosage
Cell Proliferation
/ drug effects
Dose-Response Relationship, Drug
Melanoma, Experimental
/ drug therapy
Mice
Mitochondria
/ drug effects
Oxidative Stress
/ drug effects
Reactive Oxygen Species
/ metabolism
Skin Neoplasms
/ drug therapy
Journal
Life sciences
ISSN: 1879-0631
Titre abrégé: Life Sci
Pays: Netherlands
ID NLM: 0375521
Informations de publication
Date de publication:
01 Sep 2020
01 Sep 2020
Historique:
received:
31
03
2020
revised:
11
04
2020
accepted:
14
04
2020
pubmed:
11
5
2020
medline:
1
9
2020
entrez:
11
5
2020
Statut:
ppublish
Résumé
There is a rapid increase in the incidence of melanoma which has led to a global crisis. Thus, there is a great need for developing novel, safe and effective drugs for the treatment of melanoma. Hispolon is a small molecular weight polyphenol derived from Phellinus linteus, which has antioxidant, anti-inflammatory and anti-proliferative activities. Hispolon has been reported to induce apoptosis in gastric cancer, hepatocellular carcinoma, and myeloid leukemia. However, the anticancer effect in melanoma is not well elucidated. Thus, our present study was to investigate the anti-cancer effect of hispolon on melanoma cancer cells. B16BL6 cells were treated with different concentrations of hispolon for 24 h and the effect on oxidative stress, mitochondrial functions, apoptosis and cell proliferation were studied. Hispolon is a potent generator of reactive oxygen species, nitrite and lipid peroxide levels. Furthermore, it significantly inhibits the expression of Bcl-2 and promotes the expression of Bax, increases the activity of caspase 1 and 3, inhibits mitochondrial Complex I and IV activities. By the above mechanisms, hispolon dose-dependently exhibited the antimelanoma effect similar to the well established pharmacological agent, curcumin. Thus, hispolon can be a potent anti-melanoma drug in the future if the pharmacodynamic effects and the toxicological studies are appropriately carried out.
Identifiants
pubmed: 32387411
pii: S0024-3205(20)30450-1
doi: 10.1016/j.lfs.2020.117702
pii:
doi:
Substances chimiques
Antineoplastic Agents
0
Catechols
0
Reactive Oxygen Species
0
hispolon
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
117702Informations de copyright
Copyright © 2020 Elsevier Inc. All rights reserved.