Elucidating the anti-melanoma effect and mechanisms of Hispolon.


Journal

Life sciences
ISSN: 1879-0631
Titre abrégé: Life Sci
Pays: Netherlands
ID NLM: 0375521

Informations de publication

Date de publication:
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

117702

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Ahmed Al Saqr (A)

Department of Drug Discovery and Development, Harrison School of Pharmacy, Auburn University, AL 36849; Department of Pharmaceutics, College of Pharmacy, Prince Sattam Bin Abdulaziz University, Alkharj, Saudi Arabia.

Mohammed Majrashi (M)

Department of Drug Discovery and Development, Harrison School of Pharmacy, Auburn University, AL 36849; Department of Pharmacology, Faculty of Medicine, University of Jeddah, Saudi Arabia.

Hamad Alrbyawi (H)

Department of Drug Discovery and Development, Harrison School of Pharmacy, Auburn University, AL 36849; Pharmaceutics and Pharmaceutical Technology Department, College of Pharmacy, Taibah University, Saudi Arabia.

Manoj Govindarajulu (M)

Department of Drug Discovery and Development, Harrison School of Pharmacy, Auburn University, AL 36849.

Ayaka Fujihashi (A)

Department of Drug Discovery and Development, Harrison School of Pharmacy, Auburn University, AL 36849.

Subbaraju Gottumukkala (S)

NATSOL Laboratories Private Limited, Visakhapatnam, Andhra Pradesh, India.

Ishwor Poudel (I)

Department of Drug Discovery and Development, Harrison School of Pharmacy, Auburn University, AL 36849.

Robert D Arnold (RD)

Department of Drug Discovery and Development, Harrison School of Pharmacy, Auburn University, AL 36849.

R Jayachandra Babu (RJ)

Department of Drug Discovery and Development, Harrison School of Pharmacy, Auburn University, AL 36849. Electronic address: ramapjb@auburn.edu.

Muralikrishnan Dhanasekaran (M)

Department of Drug Discovery and Development, Harrison School of Pharmacy, Auburn University, AL 36849. Electronic address: dhanamu@auburn.edu.

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Classifications MeSH