Advancements and recent explorations of anti-cancer activity of chrysin: from molecular targets to therapeutic perspective

Abhilasha Sood, Arpit Mehrotra, Ujjawal Sharma, D. Aggarwal, Tejveer Singh, M. Shahwan, A. Jairoun, Isha Rani, S. Ramniwas, H. Tuli, Vikas Yadav, Manoj Kumar
{"title":"Advancements and recent explorations of anti-cancer activity of chrysin: from molecular targets to therapeutic perspective","authors":"Abhilasha Sood, Arpit Mehrotra, Ujjawal Sharma, D. Aggarwal, Tejveer Singh, M. Shahwan, A. Jairoun, Isha Rani, S. Ramniwas, H. Tuli, Vikas Yadav, Manoj Kumar","doi":"10.37349/etat.2024.00230","DOIUrl":null,"url":null,"abstract":"In recent times, there have been notable advancements in comprehending the potential anti-cancer effects of chrysin (CH), a naturally occurring flavonoid compound found abundantly in various plant sources like honey, propolis, and certain fruits and vegetables. This active compound has garnered significant attention due to its promising therapeutic qualities and minimal toxicity. CH’s ability to combat cancer arises from its multifaceted mechanisms of action, including the initiation of apoptosis and the inhibition of proliferation, angiogenesis, metastasis, and cell cycle progression. CH also displays potent antioxidant and anti-inflammatory properties, effectively counteracting the harmful molecules that contribute to DNA damage and the development of cancer. Furthermore, CH has exhibited the potential to sensitize cancer cells to traditional chemotherapy and radiotherapy, amplifying the effectiveness of these treatments while reducing their negative impact on healthy cells. Hence, in this current review, the composition, chemistry, mechanisms of action, safety concerns of CH, along with the feasibility of its nanoformulations. To conclude, the recent investigations into CH’s anti-cancer effects present a compelling glimpse into the potential of this natural compound as a complementary therapeutic element in the array of anti-cancer approaches, providing a safer and more comprehensive method of combating this devastating ailment.","PeriodicalId":73002,"journal":{"name":"Exploration of targeted anti-tumor therapy","volume":"45 34","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Exploration of targeted anti-tumor therapy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.37349/etat.2024.00230","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

In recent times, there have been notable advancements in comprehending the potential anti-cancer effects of chrysin (CH), a naturally occurring flavonoid compound found abundantly in various plant sources like honey, propolis, and certain fruits and vegetables. This active compound has garnered significant attention due to its promising therapeutic qualities and minimal toxicity. CH’s ability to combat cancer arises from its multifaceted mechanisms of action, including the initiation of apoptosis and the inhibition of proliferation, angiogenesis, metastasis, and cell cycle progression. CH also displays potent antioxidant and anti-inflammatory properties, effectively counteracting the harmful molecules that contribute to DNA damage and the development of cancer. Furthermore, CH has exhibited the potential to sensitize cancer cells to traditional chemotherapy and radiotherapy, amplifying the effectiveness of these treatments while reducing their negative impact on healthy cells. Hence, in this current review, the composition, chemistry, mechanisms of action, safety concerns of CH, along with the feasibility of its nanoformulations. To conclude, the recent investigations into CH’s anti-cancer effects present a compelling glimpse into the potential of this natural compound as a complementary therapeutic element in the array of anti-cancer approaches, providing a safer and more comprehensive method of combating this devastating ailment.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
蛹虫草苷抗癌活性的进展与最新探索:从分子靶点到治疗视角
近来,人们在理解菊黄素(CH)的潜在抗癌作用方面取得了显著进展。菊黄素是一种天然黄酮类化合物,大量存在于蜂蜜、蜂胶和某些水果蔬菜等各种植物中。这种活性化合物因其良好的治疗效果和极低的毒性而备受关注。CH 的抗癌能力源于其多方面的作用机制,包括启动细胞凋亡和抑制细胞增殖、血管生成、转移和细胞周期进展。CH 还具有强大的抗氧化和抗炎特性,可有效抵消导致 DNA 损伤和癌症发展的有害分子。此外,CH 还显示出使癌细胞对传统化疗和放疗敏感的潜力,从而提高这些疗法的效果,同时减少其对健康细胞的负面影响。因此,本综述将对 CH 的成分、化学性质、作用机制、安全性问题以及其纳米制剂的可行性进行探讨。总之,最近对 CH 抗癌效果的研究让人们看到了这种天然化合物作为一系列抗癌方法中的补充治疗元素的潜力,为抗击这种毁灭性疾病提供了一种更安全、更全面的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
2.80
自引率
0.00%
发文量
0
审稿时长
13 weeks
期刊最新文献
Correction: Deep learning based automated epidermal growth factor receptor and anaplastic lymphoma kinase status prediction of brain metastasis in non-small cell lung cancer Advancements and recent explorations of anti-cancer activity of chrysin: from molecular targets to therapeutic perspective Resistance to immune checkpoint inhibitors in colorectal cancer with deficient mismatch repair/microsatellite instability: misdiagnosis, pseudoprogression and/or tumor heterogeneity? Immunotherapy in thymic epithelial tumors: tissue predictive biomarkers for immune checkpoint inhibitors Spheroids and organoids derived from colorectal cancer as tools for in vitro drug screening
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1