Nature's arsenal unleashed: Senegalia modesta derived thymol halts cancer progression by suppressing proangiogenic genes.

IF 1.6 3区 化学 Q3 CHEMISTRY, APPLIED Natural Product Research Pub Date : 2024-12-28 DOI:10.1080/14786419.2024.2446708
Komal Khalid, Mehr Un Nissa Bashir, Muhammad Usman Rashid, Naila Malkani
{"title":"Nature's arsenal unleashed: <i>Senegalia modesta</i> derived thymol halts cancer progression by suppressing proangiogenic genes.","authors":"Komal Khalid, Mehr Un Nissa Bashir, Muhammad Usman Rashid, Naila Malkani","doi":"10.1080/14786419.2024.2446708","DOIUrl":null,"url":null,"abstract":"<p><p>Inhibiting angiogenesis with plant-derived bioactive compounds can inhibit tumour progression. Antiangiogenic potential of <i>Senegalia modesta</i> was analysed by preparing and analysing ethanolic extracts of <i>S.modesta</i> by GC-MS and HPLC to identify bioactive components. In-vivo blood vessel formation assays in mice and chorioallantoic membrane assays (CAM) in eggs were employed to assess the antiangiogenic effects. qPCR was performed to elucidate mRNA expression of proangiogenic genes in MDA-MB-231 cells after exposure to <i>S.modesta</i> and thymol. Molecular docking analysis highlighted the interaction of thymol with VEGF receptors. <i>S.modesta</i> treatment significantly delayed wound healing in mice compared to control group. GC-MS and HPLC analyses thymol as a bioactive compound in <i>S.modesta</i> extract. CAM assay indicated reduced angiogenesis in thymol-treated groups, further confirmed by downregulation of proangiogenic genes. Molecular docking of thymol with VEGFR1/VEGFR2 revealed strong binding affinity, suggesting thymol-mediated receptor blocking. Thymol exhibits antiangiogenic potential and may serve as a promising therapeutic agent against cancer.</p>","PeriodicalId":18990,"journal":{"name":"Natural Product Research","volume":" ","pages":"1-8"},"PeriodicalIF":1.6000,"publicationDate":"2024-12-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Natural Product Research","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1080/14786419.2024.2446708","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
引用次数: 0

Abstract

Inhibiting angiogenesis with plant-derived bioactive compounds can inhibit tumour progression. Antiangiogenic potential of Senegalia modesta was analysed by preparing and analysing ethanolic extracts of S.modesta by GC-MS and HPLC to identify bioactive components. In-vivo blood vessel formation assays in mice and chorioallantoic membrane assays (CAM) in eggs were employed to assess the antiangiogenic effects. qPCR was performed to elucidate mRNA expression of proangiogenic genes in MDA-MB-231 cells after exposure to S.modesta and thymol. Molecular docking analysis highlighted the interaction of thymol with VEGF receptors. S.modesta treatment significantly delayed wound healing in mice compared to control group. GC-MS and HPLC analyses thymol as a bioactive compound in S.modesta extract. CAM assay indicated reduced angiogenesis in thymol-treated groups, further confirmed by downregulation of proangiogenic genes. Molecular docking of thymol with VEGFR1/VEGFR2 revealed strong binding affinity, suggesting thymol-mediated receptor blocking. Thymol exhibits antiangiogenic potential and may serve as a promising therapeutic agent against cancer.

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
大自然的武器库被释放:从麻茸中提取的百里酚通过抑制促血管生成基因来阻止癌症的进展。
植物源性生物活性化合物抑制血管生成可抑制肿瘤进展。采用气相色谱-质谱联用和高效液相色谱法对麻麻乙醇提取物进行了制备和分析,对其抗血管生成活性成分进行了鉴定。采用小鼠体内血管形成试验和鸡蛋绒毛膜尿囊膜试验(CAM)来评估其抗血管生成作用。采用qPCR方法,对MDA-MB-231细胞暴露于麻草和百里酚后的促血管生成基因mRNA表达进行了分析。分子对接分析强调了百里香酚与VEGF受体的相互作用。与对照组相比,麻草治疗明显延迟小鼠伤口愈合。气相色谱-质谱和高效液相色谱法分析了牡丹提取物中百里香酚的活性成分。CAM实验表明,胸腺酚处理组血管生成减少,进一步证实了促血管生成基因的下调。百里香酚与VEGFR1/VEGFR2的分子对接显示出很强的结合亲和力,提示百里香酚介导的受体阻断。百里香酚具有抗血管生成的潜力,是一种很有前途的抗癌药物。
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
Natural Product Research
Natural Product Research 化学-医药化学
CiteScore
5.10
自引率
9.10%
发文量
605
审稿时长
2.1 months
期刊介绍: The aim of Natural Product Research is to publish important contributions in the field of natural product chemistry. The journal covers all aspects of research in the chemistry and biochemistry of naturally occurring compounds. The communications include coverage of work on natural substances of land and sea and of plants, microbes and animals. Discussions of structure elucidation, synthesis and experimental biosynthesis of natural products as well as developments of methods in these areas are welcomed in the journal. Finally, research papers in fields on the chemistry-biology boundary, eg. fermentation chemistry, plant tissue culture investigations etc., are accepted into the journal. Natural Product Research issues will be subtitled either ""Part A - Synthesis and Structure"" or ""Part B - Bioactive Natural Products"". for details on this , see the forthcoming articles section. All manuscript submissions are subject to initial appraisal by the Editor, and, if found suitable for further consideration, to peer review by independent, anonymous expert referees. All peer review is single blind and submission is online via ScholarOne Manuscripts.
期刊最新文献
Research progress on chemical constituents and biological activities of medicinal plants from Euonymus genus. Experimental and computational evaluation of dinaphthodiospyrol F and dinaphthodiospyrol G from Diospyros lotus L. as ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1) inhibitors. Structural characterisation and physicochemical properties of exopolysaccharide produced by Weissella confusa P2. Discovery of secondary metabolites from the marine-derived fungus Gamszarea microspora BTBU20212050. Extraction of Phyllanthus emblica L.flavonoids by ultrasound-assisted enzymatic hydrolysis method and antioxidant stress effects.
×
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:604180095
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