Chaleshtori Zahra Monzavi, Darash Sanaz, Parsa Sarvenaz, Sarkani Elahe Orak, Taghizadeh Motahareh, Vakili Omid
Student Research Committee, School of Pharmacy and Pharmaceutical Sciences, Isfahan University of Medical Sciences, Isfahan, Iran.
Department of Clinical Biochemistry, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
Clin Chim Acta. 2025 Sep 1;577:120472. doi: 10.1016/j.cca.2025.120472. Epub 2025 Jul 8.
Bevacizumab (Avastin), a pioneering FDA-approved humanized monoclonal antibody, functions as an anti-angiogenic agent by selectively binding to all soluble isoforms of vascular endothelial growth factor-A (VEGF-A), thereby inhibiting VEGF-A receptor (VGFR) interactions on endothelial cells and disrupting critical signaling pathways for neovascularization. Preclinical in vivo studies have demonstrated that bevacizumab effectively suppresses new blood vessel formation, induces regression of immature tumor vasculature, and transiently normalizes surviving vessels, which enhances the delivery and efficacy of cytotoxic chemotherapy. Additionally, bevacizumab may exert direct antitumor effects through modulation of VEGF-A-mediated signaling pathways in malignant cells. Despite these therapeutic benefits, drug resistance remains a formidable barrier to successful cancer treatment, often resulting from complex metabolic and enzymatic alterations in tumor cells. MicroRNAs (miRNAs), small non-coding RNA (ncRNA) molecules, that regulate gene expression post-transcriptionally, have emerged as critical modulators of oncogenesis or tumor suppression by influencing processes such as inflammation, cell cycle progression, apoptosis, metastasis, and angiogenesis. Dysregulation of miRNA expression is closely linked to cancer initiation, progression, and therapeutic response. Recent evidence highlights distinct miRNA expression profiles between bevacizumab responders and non-responders, with specific miRNAs, such as miR-92b-3p, miR-10a-5p, miR-125a-5p, etc. being upregulated in patients exhibiting favorable responses. In this framework, the current review underscores the pivotal role of miRNAs in modulating cancer therapy outcomes and advocates for further research into miRNA profiling as a predictive tool to overcome drug resistance and optimize bevacizumab efficacy. Integrating miRNA analysis into clinical practice holds promise for advancing personalized cancer treatment and improving patient prognosis.
贝伐单抗(阿瓦斯汀)是一种率先获得美国食品药品监督管理局(FDA)批准的人源化单克隆抗体,它通过选择性结合血管内皮生长因子-A(VEGF-A)的所有可溶性异构体发挥抗血管生成作用,从而抑制内皮细胞上的VEGF-A受体(VGFR)相互作用,并破坏新生血管形成的关键信号通路。临床前体内研究表明,贝伐单抗能有效抑制新血管形成,诱导未成熟肿瘤血管消退,并使存活血管暂时正常化,这增强了细胞毒性化疗的递送和疗效。此外,贝伐单抗可能通过调节恶性细胞中VEGF-A介导的信号通路发挥直接抗肿瘤作用。尽管有这些治疗益处,但耐药性仍然是癌症成功治疗的巨大障碍,这通常是由肿瘤细胞中复杂的代谢和酶改变导致的。微小RNA(miRNA)是一种小的非编码RNA(ncRNA)分子,通过转录后调节基因表达,已成为肿瘤发生或肿瘤抑制的关键调节因子,影响炎症、细胞周期进程、凋亡、转移和血管生成等过程。miRNA表达失调与癌症发生、发展和治疗反应密切相关。最近的证据突出了贝伐单抗应答者和非应答者之间不同的miRNA表达谱,特定的miRNA,如miR-92b-3p、miR-10a-5p、miR-125a-5p等,在表现出良好反应的患者中上调。在此框架下,本综述强调了miRNA在调节癌症治疗结果中的关键作用,并主张进一步研究miRNA谱分析作为一种预测工具,以克服耐药性并优化贝伐单抗疗效。将miRNA分析整合到临床实践中有望推进个性化癌症治疗并改善患者预后。