Targeting ferroptosis in gastrointestinal tumors: Interplay of iron-dependent cell death and autophagy

IF 2.3 3区 生物学 Q3 BIOCHEMICAL RESEARCH METHODS Molecular and Cellular Probes Pub Date : 2025-02-01 DOI:10.1016/j.mcp.2025.102013
Mohamad Hosein Safari , Payman Rahimzadeh , Elmira Alaei , Mina Alimohammadi , Negin Esfandiari , Salman Daneshi , Neda Malgard , Najma Farahani , Afshin Taheriazam , Mehrdad Hashemi
{"title":"Targeting ferroptosis in gastrointestinal tumors: Interplay of iron-dependent cell death and autophagy","authors":"Mohamad Hosein Safari ,&nbsp;Payman Rahimzadeh ,&nbsp;Elmira Alaei ,&nbsp;Mina Alimohammadi ,&nbsp;Negin Esfandiari ,&nbsp;Salman Daneshi ,&nbsp;Neda Malgard ,&nbsp;Najma Farahani ,&nbsp;Afshin Taheriazam ,&nbsp;Mehrdad Hashemi","doi":"10.1016/j.mcp.2025.102013","DOIUrl":null,"url":null,"abstract":"<div><div>Ferroptosis is a regulated cell death mechanism distinct from apoptosis, autophagy, and necroptosis, marked by iron accumulation and lipid peroxidation. Since its identification in 2012, it has developed into a potential therapeutic target, especially concerning GI disorders like PC, HCC, GC, and CRC. This interest arises from the distinctive role of ferroptosis in the progression of diseases, presenting a new avenue for treatment where existing therapies fall short. Recent studies emphasize the promise of focusing on ferroptosis to fight GI cancers, showcasing its unique pathophysiological mechanisms compared to other types of cell death. By comprehending how ferroptosis aids in the onset and advancement of GI diseases, scientists aim to discover novel drug targets and treatment approaches. Investigating ferroptosis in gastrointestinal disorders reveals exciting possibilities for novel therapies, potentially revolutionizing cancer treatment and providing renewed hope for individuals affected by these tumors.</div></div>","PeriodicalId":49799,"journal":{"name":"Molecular and Cellular Probes","volume":"79 ","pages":"Article 102013"},"PeriodicalIF":2.3000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular and Cellular Probes","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0890850825000064","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0

Abstract

Ferroptosis is a regulated cell death mechanism distinct from apoptosis, autophagy, and necroptosis, marked by iron accumulation and lipid peroxidation. Since its identification in 2012, it has developed into a potential therapeutic target, especially concerning GI disorders like PC, HCC, GC, and CRC. This interest arises from the distinctive role of ferroptosis in the progression of diseases, presenting a new avenue for treatment where existing therapies fall short. Recent studies emphasize the promise of focusing on ferroptosis to fight GI cancers, showcasing its unique pathophysiological mechanisms compared to other types of cell death. By comprehending how ferroptosis aids in the onset and advancement of GI diseases, scientists aim to discover novel drug targets and treatment approaches. Investigating ferroptosis in gastrointestinal disorders reveals exciting possibilities for novel therapies, potentially revolutionizing cancer treatment and providing renewed hope for individuals affected by these tumors.
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
靶向胃肠道肿瘤铁下垂:铁依赖性细胞死亡和自噬的相互作用。
铁下垂是一种受调控的细胞死亡机制,不同于细胞凋亡、自噬和坏死下垂,其特征是铁积累和脂质过氧化。自2012年被发现以来,它已发展成为一种潜在的治疗靶点,特别是在PC、HCC、GC和CRC等胃肠道疾病中。这种兴趣源于铁下垂在疾病进展中的独特作用,为现有疗法不足的治疗提供了新的途径。最近的研究强调了关注铁下垂对抗胃肠道癌症的希望,展示了与其他类型的细胞死亡相比,其独特的病理生理机制。通过了解铁下垂如何帮助胃肠道疾病的发生和发展,科学家们的目标是发现新的药物靶点和治疗方法。研究胃肠道疾病中的铁下垂揭示了令人兴奋的新疗法的可能性,可能会彻底改变癌症治疗,并为受这些肿瘤影响的个体提供新的希望。
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
Molecular and Cellular Probes
Molecular and Cellular Probes 生物-生化研究方法
CiteScore
6.80
自引率
0.00%
发文量
52
审稿时长
16 days
期刊介绍: MCP - Advancing biology through–omics and bioinformatic technologies wants to capture outcomes from the current revolution in molecular technologies and sciences. The journal has broadened its scope and embraces any high quality research papers, reviews and opinions in areas including, but not limited to, molecular biology, cell biology, biochemistry, immunology, physiology, epidemiology, ecology, virology, microbiology, parasitology, genetics, evolutionary biology, genomics (including metagenomics), bioinformatics, proteomics, metabolomics, glycomics, and lipidomics. Submissions with a technology-driven focus on understanding normal biological or disease processes as well as conceptual advances and paradigm shifts are particularly encouraged. The Editors welcome fundamental or applied research areas; pre-submission enquiries about advanced draft manuscripts are welcomed. Top quality research and manuscripts will be fast-tracked.
期刊最新文献
Intestinal stem cell-derived extracellular vesicles ameliorate necrotizing enterocolitis injury A magnetic bead-based dual-aptamer sandwich assay for quantitative detection of ciprofloxacin using CRISPR/Cas12a miR-375-3p predicts the severity of endometriosis and regulates cellular progression by targeting NOX4 Rapid diagnostic testing method to detect ROB β-lactamase gene in Neisseria meningitidis Targeting the HLC-1, LC-2/ad, and PC-14 lung cancer cell lines by the silver nanoparticles green-formulated by Descurainia sophia leaf extract
×
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