Five-Decade Update on Chemopreventive and Other Pharmacological Potential of Kurarinone: a Natural Flavanone

dc.contributor.authorKumar, Shashank
dc.contributor.authorPrajapati, Kumari Sunita
dc.contributor.authorShuaib, Mohd
dc.contributor.authorKushwaha, Prem Prakash
dc.contributor.authorTuli, Hardeep Singh
dc.contributor.authorSingh, Atul Kumar
dc.date.accessioned2024-01-16T14:23:11Z
dc.date.accessioned2024-08-13T10:34:08Z
dc.date.available2024-01-16T14:23:11Z
dc.date.available2024-08-13T10:34:08Z
dc.date.issued2021-09-27T00:00:00
dc.description.abstractIn the present article we present an update on the role of chemoprevention and other pharmacological activities reported on kurarinone, a natural flavanone (from 1970 to 2021). To the best of our knowledge this is the first and exhaustive review of kurarinone. The literature was obtained from different search engine platforms including PubMed. Kurarinone possesses anticancer potential against cervical, lung (non-small and small), hepatic, esophageal, breast, gastric, cervical, and prostate cancer cells. In vivo anticancer potential of kurarinone has been extensively studied in lungs (non-small and small) using experimental xenograft models. In in vitro anticancer studies, kurarinone showed IC50 in the range of 2�62��M while in vivo efficacy was studied in the range of 20�500�mg/kg body weight of the experimental organism. The phytochemical showed higher selectivity toward cancer cells in comparison to respective normal cells. kurarinone inhibits cell cycle progression in G2/M and Sub-G1 phase in a cancer-specific context. It induces apoptosis in cancer cells by modulating molecular players involved in apoptosis/anti-apoptotic processes such as NF-?B, caspase 3/8/9/12, Bcl2, Bcl-XL, etc. The phytochemical inhibits metastasis in cancer cells by modulating the protein expression of Vimentin, N-cadherin, E-cadherin, MMP2, MMP3, and MMP9. It produces a cytostatic effect by modulating p21, p27, Cyclin D1, and Cyclin A proteins in cancer cells. Kurarinone possesses stress-mediated anticancer activity and modulates STAT3 and Akt pathways. Besides, the literature showed that kurarinone possesses anti-inflammatory, anti-drug resistance, anti-microbial (fungal, yeast, bacteria, and Coronavirus), channel and transporter modulation, neuroprotection, and estrogenic activities as well as tyrosinase/diacylglycerol acyltransferase/glucosidase/aldose reductase/human carboxylesterases 2 inhibitory potential. Kurarinone also showed therapeutic potential in the clinical study. Further, we also discussed the isolation, bioavailability, metabolism, and toxicity of Kurarinone in experimental models. � Copyright � 2021 Kumar, Prajapati, Shuaib, Kushwaha, Tuli and Singh.en_US
dc.identifier.doi10.3389/fphar.2021.737137
dc.identifier.issn16639812
dc.identifier.urihttps://doi.org/10.3389/fphar.2021.737137
dc.identifier.urihttps://kr.cup.edu.in/handle/32116/2863
dc.language.isoen_USen_US
dc.publisherFrontiers Media S.A.en_US
dc.subjectanticanceren_US
dc.subjectapoptosisen_US
dc.subjectflavanoneen_US
dc.subjectkurarinoneen_US
dc.subjectmigrationen_US
dc.subjectpharmacological activityen_US
dc.titleFive-Decade Update on Chemopreventive and Other Pharmacological Potential of Kurarinone: a Natural Flavanoneen_US
dc.title.journalFrontiers in Pharmacologyen_US
dc.typeReviewen_US
dc.type.accesstypeOpen Accessen_US

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