Withaphysalin Derivatives from Iochroma arborescens Induce Antiproliferative and Antimigratory Activities in vitro.

IF 2.1 4区 医学 Q3 CHEMISTRY, MEDICINAL Planta medica Pub Date : 2024-10-01 Epub Date: 2024-08-19 DOI:10.1055/a-2381-5060
Rodrigo Elísio de Sá, Gisele Santos de Araújo, Fabrício Dos Santos Machado, Jessica Maria Teles Souza, Ayslan Batista Barros, Francisco das Chagas Lima Pinto, Joana Deyse Lima Agostinho, Alejandro Pedro Ayala, José Delano Barreto Marinho Filho, Otília Deusdênia Loiola Pessoa, Ana Jérsia Araújo
{"title":"Withaphysalin Derivatives from Iochroma arborescens Induce Antiproliferative and Antimigratory Activities in vitro.","authors":"Rodrigo Elísio de Sá, Gisele Santos de Araújo, Fabrício Dos Santos Machado, Jessica Maria Teles Souza, Ayslan Batista Barros, Francisco das Chagas Lima Pinto, Joana Deyse Lima Agostinho, Alejandro Pedro Ayala, José Delano Barreto Marinho Filho, Otília Deusdênia Loiola Pessoa, Ana Jérsia Araújo","doi":"10.1055/a-2381-5060","DOIUrl":null,"url":null,"abstract":"<p><p>Withanolides are steroidal lactones commonly found in plants of the Solanaceae family that have significant medicinal value. In this study, three withanolides extracted from <i>Iochroma arborescens</i> leaves were isolated and characterized. These included withaphysalin F (3: ) and two newly identified epimeric compounds: 18<i>R</i>- and 18<i>S</i>-<i>O</i>-methyl-withaphysalin F (1: and 2: ). Their structures were elucidated by NMR, IR, MS, CD, and X-ray diffraction analysis, and their potential against cell proliferation and migration was investigated. The cytotoxic assay revealed activity against different tumor and non-tumor cell lines. (18<i>S</i>)-<i>O</i>-methyl-withaphysalin F (2: ) presented cell death effects after at least 6 hours of exposure. MDA-MB-231 cells were exposed to 0.06 and 0.6 µM of (18<i>S</i>)-<i>O</i>-methyl-withaphysalin F (2: ), and reductions in cell adhesion, migration, and clonogenicity were observed. Morphological analysis revealed negative regulation in filopodia, salience, and roughness, as well as alterations in cellular microarchitecture. These results provide clues as to the effects of (18<i>S</i>)-<i>O</i>-methyl-withaphysalin F (2: ), allowing new molecular modifications to improve potency and selectivity and increase our antineoplastic arsenal.</p>","PeriodicalId":20127,"journal":{"name":"Planta medica","volume":" ","pages":"938-948"},"PeriodicalIF":2.1000,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Planta medica","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1055/a-2381-5060","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/8/19 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0

Abstract

Withanolides are steroidal lactones commonly found in plants of the Solanaceae family that have significant medicinal value. In this study, three withanolides extracted from Iochroma arborescens leaves were isolated and characterized. These included withaphysalin F (3: ) and two newly identified epimeric compounds: 18R- and 18S-O-methyl-withaphysalin F (1: and 2: ). Their structures were elucidated by NMR, IR, MS, CD, and X-ray diffraction analysis, and their potential against cell proliferation and migration was investigated. The cytotoxic assay revealed activity against different tumor and non-tumor cell lines. (18S)-O-methyl-withaphysalin F (2: ) presented cell death effects after at least 6 hours of exposure. MDA-MB-231 cells were exposed to 0.06 and 0.6 µM of (18S)-O-methyl-withaphysalin F (2: ), and reductions in cell adhesion, migration, and clonogenicity were observed. Morphological analysis revealed negative regulation in filopodia, salience, and roughness, as well as alterations in cellular microarchitecture. These results provide clues as to the effects of (18S)-O-methyl-withaphysalin F (2: ), allowing new molecular modifications to improve potency and selectivity and increase our antineoplastic arsenal.

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
Iochroma arborescens 中的 Withaphysalin 衍生物在体外诱导抗增殖和抗移植物活性。
Withanolides 是茄科植物中常见的甾体内酯,具有重要的药用价值。本研究分离并鉴定了从 Iochroma arborescens 叶子中提取的三种岩白菜素内酯。其中包括岩白菜素 F(3:)和两种新鉴定的外延化合物:18R- 和 18S-O-methyl-withaphysalin F(1: 和 2: )。通过 NMR、IR、MS、CD 和 X 射线衍射分析阐明了它们的结构,并研究了它们对细胞增殖和迁移的潜力。细胞毒性试验显示了它们对不同肿瘤和非肿瘤细胞株的活性。(18S)-O-methyl-withaphysalin F (2: ) 至少暴露 6 小时后才会导致细胞死亡。MDA-MB-231 细胞暴露于 0.06 和 0.6 µM 的 (18S)-O-methyl-withaphysalin F (2: )后,细胞粘附性、迁移性和克隆生成性降低。形态学分析表明,丝状体、显著性和粗糙度出现负调控,细胞微结构也发生了改变。这些结果提供了(18S)-O-甲基石杉碱 F (2:)作用的线索,允许进行新的分子修饰以提高效力和选择性,并增加我们的抗肿瘤药物库。
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
Planta medica
Planta medica 医学-药学
CiteScore
5.10
自引率
3.70%
发文量
101
审稿时长
1.8 months
期刊介绍: Planta Medica is one of the leading international journals in the field of natural products – including marine organisms, fungi as well as micro-organisms – and medicinal plants. Planta Medica accepts original research papers, reviews, minireviews and perspectives from researchers worldwide. The journal publishes 18 issues per year. The following areas of medicinal plants and natural product research are covered: -Biological and Pharmacological Activities -Natural Product Chemistry & Analytical Studies -Pharmacokinetic Investigations -Formulation and Delivery Systems of Natural Products. The journal explicitly encourages the submission of chemically characterized extracts.
期刊最新文献
New constituents from Zanthoxylum rhoifolium Lam. Phytochemical characterization and comparative analysis of cycloartane-type triterpenes in Astragalus adsurgens and Astragalus membranaceus. Aloe vera and the Proliferative Phase of Cutaneous Wound Healing: Status Quo Report on Active Principles, Mechanisms, and Applications. Turkish Astragalus Species: Botanical Aspects, Secondary Metabolites, and Biotransformation. Betulinic Acid Acts in Synergism with Imatinib Mesylate, Triggering Apoptosis in MDR Leukemia Cells.
×
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