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Uncovering the Anticancer Potential of Polydatin: A Mechanistic Insight

Uncovering the Anticancer Potential of Polydatin: A Mechanistic Insight

Authors :
Muhammad Ajmal Shah
Ayesha Hamid
Hafiza Ishmal Faheem
Azhar Rasul
Tourki A. S. Baokbah
Muhammad Haris
Rimsha Yousaf
Uzma Saleem
Shabnoor Iqbal
Maria Silvana Alves
Zahid Khan
Ghulam Hussain
Ifat Alsharfi
Haroon Khan
Philippe Jeandet
Source :
Molecules, Vol 27, Iss 21, p 7175 (2022)
Publication Year :
2022
Publisher :
MDPI AG, 2022.

Abstract

Polydatin or 3-O-β-d-resveratrol-glucopyranoside (PD), a stilbenoid component of Polygonum cuspicadum (Polygonaceae), has a variety of biological roles. In traditional Chinese medicine, P. cuspicadum extracts are used for the treatment of infections, inflammation, and cardiovascular disorders. Polydatin possesses a broad range of biological activities including antioxidant, anti-inflammatory, anticancer, and hepatoprotective, neuroprotective, and immunostimulatory effects. Currently, a major proportion of the population is victimized with cervical lung cancer, ovarian cancer and breast cancer. PD has been recognized as a potent anticancer agent. PD could effectively inhibit the migration and proliferation of ovarian cancer cells, as well as the expression of the PI3K protein. The malignancy of lung cancer cells was reduced after PD treatments via targeting caspase 3, arresting cancer cells at the S phase and inhibiting NLRP3 inflammasome by downregulation of the NF-κB pathway. This ceases cell cycle, inhibits VEGF, and counteracts ROS in breast cancer. It also prevents cervical cancer by regulating epithelial-to-mesenchymal transition (EMT), apoptosis, and the C-Myc gene. The objective of this review is thus to unveil the polydatin anticancer potential for the treatment of various tumors, as well as to examine the mechanisms of action of this compound.

Details

Language :
English
ISSN :
27217175 and 14203049
Volume :
27
Issue :
21
Database :
Directory of Open Access Journals
Journal :
Molecules
Publication Type :
Academic Journal
Accession number :
edsdoj.4666d5e3a70944ef8462878c6ed5ef14
Document Type :
article
Full Text :
https://doi.org/10.3390/molecules27217175