Artemisinin and its derivatives: a promising cancer therapy.


Journal

Molecular biology reports
ISSN: 1573-4978
Titre abrégé: Mol Biol Rep
Pays: Netherlands
ID NLM: 0403234

Informations de publication

Date de publication:
Aug 2020
Historique:
received: 09 04 2020
accepted: 15 07 2020
pubmed: 28 7 2020
medline: 27 5 2021
entrez: 26 7 2020
Statut: ppublish

Résumé

The world is experiencing a cancer epidemic and an increase in the prevalence of the disease. Cancer remains a major killer, accounting for more than half a million deaths annually. There is a wide range of natural products that have the potential to treat this disease. One of these products is artemisinin; a natural product from Artemisia plant. The Nobel Prize for Medicine was awarded in 2015 for the discovery of artemisinin in recognition of the drug's efficacy. Artemisinin produces highly reactive free radicals by the breakdown of two oxygen atoms that kill cancerous cells. These cells sequester iron and accumulate as much as 1000 times in comparison with normal cells. Generally, chemotherapy is toxic to both cancerous cells and normal cells, while no significant cytotoxicity from artemisinin to normal cells has been found in more than 4000 case studies, which makes it far different than conventional chemotherapy. The pleiotropic response of artemisinin in cancer cells is responsible for growth inhibition by multiple ways including inhibition of angiogenesis, apoptosis, cell cycle arrest, disruption of cell migration, and modulation of nuclear receptor responsiveness. It is very encouraging that artemisinin and its derivatives are anticipated to be a novel class of broad-spectrum antitumor agents based on efficacy and safety. This review aims to highlight these achievements and propose potential strategies to develop artemisinin and its derivatives as a new class of cancer therapeutic agents.

Identifiants

pubmed: 32710388
doi: 10.1007/s11033-020-05669-z
pii: 10.1007/s11033-020-05669-z
doi:

Substances chimiques

Antineoplastic Agents 0
Artemisinins 0
artemisinin 9RMU91N5K2

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

6321-6336

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Auteurs

Bushra Hafeez Kiani (BH)

Department of Biological Sciences, Faculty of Basic and Applied Sciences, International Islamic University, Islamabad, 44000, Pakistan. bushra.hafeez@iiu.edu.pk.

Waqas Khan Kayani (WK)

Department of Plant Breeding, Swedish University of Agricultural Sciences, Växtskyddsvägen 1, 23053, Alnarp, Sweden.

Asma Umer Khayam (AU)

Department of Biochemistry, Faculty of Biological Sciences, Quaid-I-Azam University, Islamabad, 45320, Pakistan.

Erum Dilshad (E)

Department of Bioinformatics and Biosciences, Capital University of Science and Technology, Islamabad, Pakistan.

Hammad Ismail (H)

Department of Biochemistry and Molecular Biology, University of Gujrat, Gujrat, 50700, Pakistan.

Bushra Mirza (B)

Department of Biochemistry, Faculty of Biological Sciences, Quaid-I-Azam University, Islamabad, 45320, Pakistan.

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