Investigation of the regulation of EGF signaling by miRNAs, delving into the underlying mechanism and signaling pathways in cancer

IF 3.3 3区 生物学 Q3 CELL BIOLOGY Experimental cell research Pub Date : 2024-09-21 DOI:10.1016/j.yexcr.2024.114267
Darmadi Darmadi , Zafar Aminov , Ahmed Hjazi , Roopashree R , Syeda Wajida Kazmi , Yasser Fakri Mustafa , Beneen Hosseen , Abhishek Sharma , Mahmood Hasen Shuhata Alubiady , Salah Hassan Zain Al-Abdeen
{"title":"Investigation of the regulation of EGF signaling by miRNAs, delving into the underlying mechanism and signaling pathways in cancer","authors":"Darmadi Darmadi ,&nbsp;Zafar Aminov ,&nbsp;Ahmed Hjazi ,&nbsp;Roopashree R ,&nbsp;Syeda Wajida Kazmi ,&nbsp;Yasser Fakri Mustafa ,&nbsp;Beneen Hosseen ,&nbsp;Abhishek Sharma ,&nbsp;Mahmood Hasen Shuhata Alubiady ,&nbsp;Salah Hassan Zain Al-Abdeen","doi":"10.1016/j.yexcr.2024.114267","DOIUrl":null,"url":null,"abstract":"<div><div>The EGF receptors (EGFRs) signaling pathway is essential for tumorigenesis and progression of cancer. Emerging evidence suggests that miRNAs are essential regulators of EGF signaling, influencing various pathway components and tumor behavior. This article discusses the underlying mechanisms and clinical implications of miRNA-mediated regulation of EGF signaling in cancer. miRNAs utilize multiple mechanisms to exert their regulatory effects on EGF signaling. They can target EGF ligands, including EGF and TGF-directly, inhibiting their expression and secretion. In addition, miRNAs can modulate EGF signaling indirectly by targeting EGF receptors, downstream signaling molecules, and transcription factors implicated in regulating the EGF pathway. These miRNAs can disrupt the delicate equilibrium of EGF signaling, resulting in aberrant activation and fostering tumor cell proliferation, survival, angiogenesis, and metastasis. The dysregulation of the expression of specific miRNAs has been linked to clinical outcomes in numerous types of cancer. Specific profiles of miRNA expression have been identified as prognostic markers, reflecting tumor characteristics, invasiveness, metastatic potential, and therapeutic response. These miRNAs can serve as potential therapeutic targets for interventions that modulate EGF signaling and improve patient outcomes. Understanding the intricate relationship between miRNAs and EGF signaling in cancer can transform cancer diagnosis, prognosis, and treatment. The identification of specific miRNAs involved in the regulation of the EGF pathway opens the door to the development of targeted therapies and personalized medicine approaches. In addition, miRNA-based interventions promise to overcome therapeutic resistance and improve the efficacy of existing treatments. miRNAs are crucial regulators of EGF signaling in cancer, affecting tumor behavior and clinical outcomes. Further research is required to decipher the complex network of miRNA-mediated EGF signaling regulation and translate these findings into clinically applicable strategies for enhanced cancer treatment.</div></div>","PeriodicalId":12227,"journal":{"name":"Experimental cell research","volume":"442 2","pages":"Article 114267"},"PeriodicalIF":3.3000,"publicationDate":"2024-09-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Experimental cell research","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0014482724003586","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The EGF receptors (EGFRs) signaling pathway is essential for tumorigenesis and progression of cancer. Emerging evidence suggests that miRNAs are essential regulators of EGF signaling, influencing various pathway components and tumor behavior. This article discusses the underlying mechanisms and clinical implications of miRNA-mediated regulation of EGF signaling in cancer. miRNAs utilize multiple mechanisms to exert their regulatory effects on EGF signaling. They can target EGF ligands, including EGF and TGF-directly, inhibiting their expression and secretion. In addition, miRNAs can modulate EGF signaling indirectly by targeting EGF receptors, downstream signaling molecules, and transcription factors implicated in regulating the EGF pathway. These miRNAs can disrupt the delicate equilibrium of EGF signaling, resulting in aberrant activation and fostering tumor cell proliferation, survival, angiogenesis, and metastasis. The dysregulation of the expression of specific miRNAs has been linked to clinical outcomes in numerous types of cancer. Specific profiles of miRNA expression have been identified as prognostic markers, reflecting tumor characteristics, invasiveness, metastatic potential, and therapeutic response. These miRNAs can serve as potential therapeutic targets for interventions that modulate EGF signaling and improve patient outcomes. Understanding the intricate relationship between miRNAs and EGF signaling in cancer can transform cancer diagnosis, prognosis, and treatment. The identification of specific miRNAs involved in the regulation of the EGF pathway opens the door to the development of targeted therapies and personalized medicine approaches. In addition, miRNA-based interventions promise to overcome therapeutic resistance and improve the efficacy of existing treatments. miRNAs are crucial regulators of EGF signaling in cancer, affecting tumor behavior and clinical outcomes. Further research is required to decipher the complex network of miRNA-mediated EGF signaling regulation and translate these findings into clinically applicable strategies for enhanced cancer treatment.
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
研究 miRNA 对 EGF 信号的调控,深入探讨癌症的内在机制和信号通路。
表皮生长因子受体(表皮生长因子受体)信号通路对肿瘤的发生和发展至关重要。新的证据表明,miRNA 是表皮生长因子受体信号通路的重要调控因子,可影响信号通路的各种成分和肿瘤行为。本文探讨了 miRNA 介导的癌症中 EGF 信号转导调控的内在机制和临床意义。它们可以直接靶向 EGF 配体,包括 EGF 和 TGF,抑制它们的表达和分泌。此外,miRNAs 还可以通过靶向 EGF 受体、下游信号分子和参与调节 EGF 通路的转录因子,间接调节 EGF 信号。这些 miRNA 可破坏 EGF 信号的微妙平衡,导致异常激活,促进肿瘤细胞增殖、存活、血管生成和转移。特定 miRNA 的表达失调与多种癌症的临床结果有关。特定的 miRNA 表达谱已被确定为预后标志物,可反映肿瘤特征、侵袭性、转移潜力和治疗反应。这些 miRNA 可作为潜在的治疗靶点,用于调节表皮生长因子信号转导和改善患者预后的干预措施。了解癌症中 miRNA 与表皮生长因子信号转导之间错综复杂的关系可以改变癌症诊断、预后和治疗。确定参与 EGF 通路调控的特定 miRNA 为开发靶向疗法和个性化医疗方法打开了大门。此外,基于 miRNA 的干预措施有望克服治疗耐药性,提高现有疗法的疗效。miRNA 是癌症中表皮生长因子信号转导的关键调控因子,会影响肿瘤行为和临床结果。要破译 miRNA 介导的表皮生长因子信号调控的复杂网络,并将这些发现转化为临床适用的策略以加强癌症治疗,还需要进一步的研究。
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
Experimental cell research
Experimental cell research 医学-细胞生物学
CiteScore
7.20
自引率
0.00%
发文量
295
审稿时长
30 days
期刊介绍: Our scope includes but is not limited to areas such as: Chromosome biology; Chromatin and epigenetics; DNA repair; Gene regulation; Nuclear import-export; RNA processing; Non-coding RNAs; Organelle biology; The cytoskeleton; Intracellular trafficking; Cell-cell and cell-matrix interactions; Cell motility and migration; Cell proliferation; Cellular differentiation; Signal transduction; Programmed cell death.
期刊最新文献
DDX18 influences chemotherapy sensitivity in colorectal cancer by regulating genomic stability. A semi-permeable insert culture model for the distal part of the nephron with human and mouse tubuloid epithelial cells. Seven Theorems of Joseph G. Gall. Knockdown of Leucine-rich alpha-2-glycoprotein 1 alleviates renal ischemia-reperfusion injury by inhibiting NOX4-mediated apoptosis, inflammation, and oxidative stress. Hyaluronic acid-modified extracellular vesicles for targeted doxorubicin delivery in hepatocellular carcinoma
×
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