利用计算机方法鉴定宫颈癌中强效黄酮类化合物的靶向治疗方法。

Srishti Sharma, Anuja Mishra, Pratibha Pandey
{"title":"利用计算机方法鉴定宫颈癌中强效黄酮类化合物的靶向治疗方法。","authors":"Srishti Sharma, Anuja Mishra, Pratibha Pandey","doi":"10.2174/0118715303362788250616052258","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>The prevalence of cervical cancer has substantially increased, leading to global apprehension. The signaling pathway governs many cellular differentiation processes that occur during embryonic development and adulthood.</p><p><strong>Aim: </strong>Our study has mostly focused on discovering inhibitory plant chemicals, specifically flavonoids, that can block the Notch signaling pathway owing to the numerous adverse effects associated with standard treatments. Thus far, only a few studies have documented these specific flavonoids' ability to inhibit the three essential targets of the Notch signaling system in cervical cancer.</p><p><strong>Methodology: </strong>This study aimed to assess the inhibitory potential of twenty-five potent flavonoids against the Notch signaling pathway components in cervical cancer using various in silico meth ods.</p><p><strong>Results: </strong>Of all the compounds tested, naringenin exhibited the most favorable binding energy (with concrete free binding energy value) against jagged2, notch 2, and notch 3 in cervical cancer.</p><p><strong>Conclusion: </strong>Naringenin could further be evaluated for its anticancer potential in cervical cancer via employing in vitro approaches. To overcome the limitations of current chemotherapeutic procedures, developing naringenin as a novel anticancer drug requires a systematic and strategic approach to rational drug discovery that is both efficient and cost-effective.</p>","PeriodicalId":94316,"journal":{"name":"Endocrine, metabolic & immune disorders drug targets","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Targeted Therapeutic Approach Employing <i>In Silico</i> Methods to Identify Potent Flavonoids in Cervical Cancer.\",\"authors\":\"Srishti Sharma, Anuja Mishra, Pratibha Pandey\",\"doi\":\"10.2174/0118715303362788250616052258\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>The prevalence of cervical cancer has substantially increased, leading to global apprehension. The signaling pathway governs many cellular differentiation processes that occur during embryonic development and adulthood.</p><p><strong>Aim: </strong>Our study has mostly focused on discovering inhibitory plant chemicals, specifically flavonoids, that can block the Notch signaling pathway owing to the numerous adverse effects associated with standard treatments. Thus far, only a few studies have documented these specific flavonoids' ability to inhibit the three essential targets of the Notch signaling system in cervical cancer.</p><p><strong>Methodology: </strong>This study aimed to assess the inhibitory potential of twenty-five potent flavonoids against the Notch signaling pathway components in cervical cancer using various in silico meth ods.</p><p><strong>Results: </strong>Of all the compounds tested, naringenin exhibited the most favorable binding energy (with concrete free binding energy value) against jagged2, notch 2, and notch 3 in cervical cancer.</p><p><strong>Conclusion: </strong>Naringenin could further be evaluated for its anticancer potential in cervical cancer via employing in vitro approaches. To overcome the limitations of current chemotherapeutic procedures, developing naringenin as a novel anticancer drug requires a systematic and strategic approach to rational drug discovery that is both efficient and cost-effective.</p>\",\"PeriodicalId\":94316,\"journal\":{\"name\":\"Endocrine, metabolic & immune disorders drug targets\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-06-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Endocrine, metabolic & immune disorders drug targets\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2174/0118715303362788250616052258\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Endocrine, metabolic & immune disorders drug targets","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/0118715303362788250616052258","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

背景:宫颈癌的患病率大幅上升,导致全球担忧。信号通路控制着胚胎发育和成年期间发生的许多细胞分化过程。目的:我们的研究主要集中在发现抑制性植物化学物质,特别是类黄酮,它可以阻断Notch信号通路,这是由于与标准治疗相关的许多不良反应。到目前为止,只有少数研究证明了这些特定的类黄酮能够抑制宫颈癌中Notch信号系统的三个基本靶点。方法:本研究旨在利用不同的硅片方法评估25种强效黄酮类化合物对宫颈癌Notch信号通路成分的抑制潜力。结果:柚皮素对宫颈癌的jagged2、notch 2和notch 3具有较好的结合能(具有具体的自由结合能值)。结论:柚皮素对宫颈癌的抗肿瘤作用可通过体外实验进一步评价。为了克服目前化疗程序的局限性,开发柚皮素作为一种新的抗癌药物需要一个系统的和战略性的方法来合理地发现药物,既有效又经济。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Targeted Therapeutic Approach Employing In Silico Methods to Identify Potent Flavonoids in Cervical Cancer.

Background: The prevalence of cervical cancer has substantially increased, leading to global apprehension. The signaling pathway governs many cellular differentiation processes that occur during embryonic development and adulthood.

Aim: Our study has mostly focused on discovering inhibitory plant chemicals, specifically flavonoids, that can block the Notch signaling pathway owing to the numerous adverse effects associated with standard treatments. Thus far, only a few studies have documented these specific flavonoids' ability to inhibit the three essential targets of the Notch signaling system in cervical cancer.

Methodology: This study aimed to assess the inhibitory potential of twenty-five potent flavonoids against the Notch signaling pathway components in cervical cancer using various in silico meth ods.

Results: Of all the compounds tested, naringenin exhibited the most favorable binding energy (with concrete free binding energy value) against jagged2, notch 2, and notch 3 in cervical cancer.

Conclusion: Naringenin could further be evaluated for its anticancer potential in cervical cancer via employing in vitro approaches. To overcome the limitations of current chemotherapeutic procedures, developing naringenin as a novel anticancer drug requires a systematic and strategic approach to rational drug discovery that is both efficient and cost-effective.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信