Unveiling the Anti-cancer Potential of Vulpinic Acid: A Selective Therapeutic Agent Against Oral Squamous Cell Carcinoma.

IF 3.5 4区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Dilara Nur Şengüm, Ayşe Hale Alkan, Fatma Zeynep Bozkurt, Pelin Mutlu, Demet Cansaran-Duman
{"title":"Unveiling the Anti-cancer Potential of Vulpinic Acid: A Selective Therapeutic Agent Against Oral Squamous Cell Carcinoma.","authors":"Dilara Nur Şengüm, Ayşe Hale Alkan, Fatma Zeynep Bozkurt, Pelin Mutlu, Demet Cansaran-Duman","doi":"10.2174/0109298673440776260127212434","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Lip and oral cavity cancers are among the most common types of cancer worldwide and remain a major health problem due to poor prognosis and treatment- related side effects. Therefore, identifying new naturally derived compounds with selective cytotoxic effects on oral cancer cells is essential. Vulpinic acid, a lichenderived secondary metabolite, has shown antioxidant and anticancer activities in various cancer types. However, its effects on oral cancer cells have not yet been clarified. This study aims to investigate the cytotoxic and apoptotic effects of vulpinic acid on oral cancer cells and to explore its possible molecular mechanisms.</p><p><strong>Methods: </strong>The cytotoxic effect of vulpinic acid on OSC-19 oral cancer and MRC-5 normal fibroblast cells was assessed using xCELLigence analysis. The impact of vulpinic acid on cell cycle progression, apoptotic mechanisms, colony formation, wound healing, and molecular-level effects was analyzed using flow cytometry, mitochondrial membrane potential assay, and qRT-PCR. The effect of vulpinic acid on BIRC5 protein levels was further confirmed by western blot analysis.</p><p><strong>Results: </strong>The results showed that the IC50 value of vulpinic acid was 59 μM in OSC-19 cells and 114 μM in MRC-5 cells, demonstrating its selective cytotoxic effect on oral cancer cells. Vulpinic acid treatment suppressed colony formation by 55.5% and reduced cell migration by 71.2-fold at 96 h. Cell cycle analysis revealed that vulpinic acid induced G1 phase arrest, while apoptosis analysis showed a decrease in mitochondrial membrane potential. qRT-PCR analysis revealed an upregulation of pro-apoptotic genes (BID, CASP4, CASP7, BAK1, BCL2L2) and downregulation of the anti-apoptotic gene survivin (BIRC5). According to western blot analysis, BIRC5 protein expression decreased 2.39-fold following vulpinic acid treatment.</p><p><strong>Discussion: </strong>These findings indicate that vulpinic acid has the potential to be considered as an anti-cancer agent.</p><p><strong>Conclusion: </strong>Further in vivo and clinical studies are required to validate its therapeutic efficacy and safety profile.</p>","PeriodicalId":10984,"journal":{"name":"Current medicinal chemistry","volume":" ","pages":""},"PeriodicalIF":3.5000,"publicationDate":"2026-05-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current medicinal chemistry","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.2174/0109298673440776260127212434","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: Lip and oral cavity cancers are among the most common types of cancer worldwide and remain a major health problem due to poor prognosis and treatment- related side effects. Therefore, identifying new naturally derived compounds with selective cytotoxic effects on oral cancer cells is essential. Vulpinic acid, a lichenderived secondary metabolite, has shown antioxidant and anticancer activities in various cancer types. However, its effects on oral cancer cells have not yet been clarified. This study aims to investigate the cytotoxic and apoptotic effects of vulpinic acid on oral cancer cells and to explore its possible molecular mechanisms.

Methods: The cytotoxic effect of vulpinic acid on OSC-19 oral cancer and MRC-5 normal fibroblast cells was assessed using xCELLigence analysis. The impact of vulpinic acid on cell cycle progression, apoptotic mechanisms, colony formation, wound healing, and molecular-level effects was analyzed using flow cytometry, mitochondrial membrane potential assay, and qRT-PCR. The effect of vulpinic acid on BIRC5 protein levels was further confirmed by western blot analysis.

Results: The results showed that the IC50 value of vulpinic acid was 59 μM in OSC-19 cells and 114 μM in MRC-5 cells, demonstrating its selective cytotoxic effect on oral cancer cells. Vulpinic acid treatment suppressed colony formation by 55.5% and reduced cell migration by 71.2-fold at 96 h. Cell cycle analysis revealed that vulpinic acid induced G1 phase arrest, while apoptosis analysis showed a decrease in mitochondrial membrane potential. qRT-PCR analysis revealed an upregulation of pro-apoptotic genes (BID, CASP4, CASP7, BAK1, BCL2L2) and downregulation of the anti-apoptotic gene survivin (BIRC5). According to western blot analysis, BIRC5 protein expression decreased 2.39-fold following vulpinic acid treatment.

Discussion: These findings indicate that vulpinic acid has the potential to be considered as an anti-cancer agent.

Conclusion: Further in vivo and clinical studies are required to validate its therapeutic efficacy and safety profile.

揭示口服鳞状细胞癌选择性治疗剂Vulpinic Acid的抗癌潜力。
简介:唇癌和口腔癌是世界上最常见的癌症类型之一,由于预后差和治疗相关的副作用,仍然是一个主要的健康问题。因此,鉴定出对口腔癌细胞具有选择性细胞毒性作用的新的天然化合物是必要的。Vulpinic acid是地衣衍生的次级代谢物,在多种癌症中显示出抗氧化和抗癌活性。然而,其对口腔癌细胞的作用尚未明确。本研究旨在探讨vulpinic acid对口腔癌细胞的细胞毒和凋亡作用,并探讨其可能的分子机制。方法:采用xCELLigence法观察vulpinic酸对OSC-19口腔癌和MRC-5正常成纤维细胞的细胞毒作用。利用流式细胞术、线粒体膜电位测定和qRT-PCR分析vulpinic酸对细胞周期进程、凋亡机制、菌落形成、伤口愈合和分子水平效应的影响。western blot分析进一步证实了vulpinic acid对BIRC5蛋白水平的影响。结果:vulpinic acid对OSC-19细胞的IC50值为59 μM,对MRC-5细胞的IC50值为114 μM,显示了其对口腔癌细胞的选择性细胞毒作用。在96 h时,Vulpinic酸抑制了55.5%的集落形成,减少了71.2倍的细胞迁移。细胞周期分析显示,Vulpinic酸诱导G1期阻滞,而凋亡分析显示线粒体膜电位下降。qRT-PCR分析显示,促凋亡基因(BID、CASP4、CASP7、BAK1、BCL2L2)上调,抗凋亡基因survivin (BIRC5)下调。western blot分析显示,vulpinic酸处理后,BIRC5蛋白表达降低2.39倍。讨论:这些发现表明,vulpinic酸有潜力被认为是一种抗癌剂。结论:需要进一步的体内和临床研究来验证其治疗效果和安全性。
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 求助全文
来源期刊
Current medicinal chemistry
Current medicinal chemistry 医学-生化与分子生物学
CiteScore
8.60
自引率
2.40%
发文量
468
审稿时长
3 months
期刊介绍: Aims & Scope Current Medicinal Chemistry covers all the latest and outstanding developments in medicinal chemistry and rational drug design. Each issue contains a series of timely in-depth reviews and guest edited thematic issues written by leaders in the field covering a range of the current topics in medicinal chemistry. The journal also publishes reviews on recent patents. Current Medicinal Chemistry is an essential journal for every medicinal chemist who wishes to be kept informed and up-to-date with the latest and most important developments.
×
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
小红书