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。

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
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引用次数: 0

摘要

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。
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Investigation of the regulation of EGF signaling by miRNAs, delving into the underlying mechanism and signaling pathways in cancer
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.
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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.
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Editorial Board The cystogenic effects of ouabain in autosomal dominant polycystic kidney disease require cell caveolae. Fbxo11 maintains mitochondrial function and prevents podocyte injury in adriamycin-induced nephropathy by mediating the ubiquitin degradation of Fosl2. MOTS-c relieves hepatocellular carcinoma resistance to TRAIL-induced apoptosis under hypoxic conditions by activating MEF2A DDX18 influences chemotherapy sensitivity in colorectal cancer by regulating genomic stability
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