Please use this identifier to cite or link to this item: https://doi.org/10.3390/molecules24040734
Title: Potential of zerumbone as an anti-cancer agent
Authors: Girisa, S.
Shabnam, B.
Monisha, J.
Fan, L. 
Halim, C.E. 
Arfuso, F.
Ahn, K.S.
Sethi, G. 
Kunnumakkara, A.B.
Keywords: Akt
Apoptosis
Cancer
FOXO1
IL-6/JAK2/STAT3
NF-?B
Zerumbone
Issue Date: 2019
Publisher: MDPI AG
Citation: Girisa, S., Shabnam, B., Monisha, J., Fan, L., Halim, C.E., Arfuso, F., Ahn, K.S., Sethi, G., Kunnumakkara, A.B. (2019). Potential of zerumbone as an anti-cancer agent. Molecules 24 (4) : 734. ScholarBank@NUS Repository. https://doi.org/10.3390/molecules24040734
Rights: Attribution 4.0 International
Abstract: Cancer is still a major risk factor to public health globally, causing approximately 9.8 million deaths worldwide in 2018. Despite advances in conventional treatment modalities for cancer treatment, there are still few effective therapies available due to the lack of selectivity, adverse side effects, non-specific toxicities, and tumour recurrence. Therefore, there is an immediate need for essential alternative therapeutics, which can prove to be beneficial and safe against cancer. Various phytochemicals from natural sources have been found to exhibit beneficial medicinal properties against various human diseases. Zerumbone is one such compound isolated from Zingiber zerumbet Smith that possesses diverse pharmacological properties including those of antioxidant, antibacterial, antipyretic, anti-inflammatory, immunomodulatory, as well as anti-neoplastic. Zerumbone has shown its anti-cancer effects by causing significant suppression of proliferation, survival, angiogenesis, invasion, and metastasis through the molecular modulation of different pathways such as NF-?B, Akt, and IL-6/JAK2/STAT3 (interleukin-6/janus kinase-2/signal transducer and activator of transcription 3) and their downstream target proteins. The current review briefly summarizes the modes of action and therapeutic potential of zerumbone against various cancers. © 2019 by the authors.
Source Title: Molecules
URI: https://scholarbank.nus.edu.sg/handle/10635/209598
ISSN: 1420-3049
DOI: 10.3390/molecules24040734
Rights: Attribution 4.0 International
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