Physcion and Physcion 8-O-β-D-glucopyranoside: Natural Anthraquinones with Potential Anticancer Activities.

Physcion anthraquinone anticancer chemosensitization natural products physcion 8-O-β-D-glucopyranoside

Journal

Current drug targets
ISSN: 1873-5592
Titre abrégé: Curr Drug Targets
Pays: United Arab Emirates
ID NLM: 100960531

Informations de publication

Date de publication:
2021
Historique:
received: 06 03 2020
revised: 18 05 2020
accepted: 09 06 2020
pubmed: 15 10 2020
medline: 27 11 2021
entrez: 14 10 2020
Statut: ppublish

Résumé

Nature has provided prodigious reservoirs of pharmacologically active compounds for drug development since times. Physcion and physcion 8-O-β-D-glucopyranoside (PG) are bioactive natural anthraquinones which exert anti-inflammatory and anticancer properties with minimum or no adverse effects. Moreover, physcion also exhibits anti-microbial and hepatoprotective properties, while PG is known to have anti-sepsis as well as ameliorative activities against dementia. This review aims to highlight the natural sources and anticancer activities of physcion and PG, along with associated mechanisms of actions. On the basis of the literature, physcion and PG regulate multitudinous cell signaling pathways through the modulation of various regulators of cell cycle, protein kinases, microRNAs, transcriptional factors, and apoptosis linked proteins resulting in the effective killing of cancerous cells in vitro as well as in vivo. Both compounds effectively suppress metastasis, furthermore, physcion acts as an inhibitor of 6PGD and also plays an important role in chemosensitization. This review article suggests that physcion and PG are potent anticancer drug candidates, but further investigations on their mechanism of action and pre-clinical trials are mandatory in order to comprehend the full potential of these natural cancer killers in anticancer remedies.

Identifiants

pubmed: 33050858
pii: CDT-EPUB-110643
doi: 10.2174/1389450121999201013154542
doi:

Substances chimiques

Antineoplastic Agents 0
Glucosides 0
physcion 8-O-glucopyranoside 0
physcione H6PT94IV61
Emodin KA46RNI6HN

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

488-504

Informations de copyright

Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

Auteurs

Muhammad Adnan (M)

Department of Zoology, Faculty of Life Sciences, Government College University, Faisalabad, Pakistan.

Azhar Rasul (A)

Department of Zoology, Faculty of Life Sciences, Government College University, Faisalabad, Pakistan.

Ghulam Hussain (G)

Department of Physiology, Faculty of Life Sciences, Government College University, Faisalabad, Pakistan.

Muhammad Ajmal Shah (MA)

Department of Pharmacognosy, Faculty of Pharmaceutical Sciences, Government College University, Faisalabad, Pakistan.

Iqra Sarfraz (I)

Department of Zoology, Faculty of Life Sciences, Government College University, Faisalabad, Pakistan.

Bushra Nageen (B)

Department of Zoology, Faculty of Life Sciences, Government College University, Faisalabad, Pakistan.

Ammara Riaz (A)

Department of Zoology, Faculty of Life Sciences, Government College University, Faisalabad, Pakistan.

Rida Khalid (R)

Department of Zoology, Faculty of Life Sciences, Government College University, Faisalabad, Pakistan.

Muhammad Asrar (M)

Department of Zoology, Faculty of Life Sciences, Government College University, Faisalabad, Pakistan.

Zeliha Selamoglu (Z)

Department of Medical Biology, Faculty of Medicine, Nigde Ömer Halisdemir University, Nigde, Campus 51240, Turkey.

Şevki Adem (Ş)

Department of Chemistry, Faculty of Sciences, Cankiri Karatekin University, UluyazI Campus Cankiri, Turkey.

Satyajit D Sarker (SD)

School of Pharmacy & Biomolecular Sciences, Liverpool John Moores University, England, United Kingdom.

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Classifications MeSH