Conceptualization of fibroblast growth factor receptor 1 targeting nanomedicines.

Q3 Medicine
Exploration of targeted anti-tumor therapy Pub Date : 2025-12-17 eCollection Date: 2025-01-01 DOI:10.37349/etat.2025.1002353
Yilin Ma, Mengqin Guo, Yang Liu, Zhengwei Huang
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引用次数: 0

Abstract

Fibroblast growth factor receptor 1 (FGFR1) is crucial in the progression of various cancers, participating in the processes of cell proliferation, survival, and differentiation. FGFR1 plays a role in the resistance to immune checkpoint inhibitors (ICIs) such as pembrolizumab and nivolumab. Therefore, using monoclonal antibodies and tyrosine kinase inhibitors to target FGFR1 and enhancing ICIs by modifying the tumor microenvironment and combating immune suppression represents a potential therapeutic strategy. Based on the FGFR1-related research and the active targeting strategy, we believe that modifying the surface of nanomedicines with anti-FGFR1 antibodies (such as OM-RCA-01) is an effective targeted treatment method for tumors with high expression of FGFR1. Although there have been relevant studies confirming the feasibility of this approach, there are challenges in clinical application, especially in terms of maintaining uniform quality during large-scale production. Therefore, we suggest conducting further optimization studies in the future to accelerate the clinical application of such drug delivery systems and provide more efficient and cost-effective options for tumor treatment.

Abstract Image

Abstract Image

Abstract Image

靶向纳米药物的成纤维细胞生长因子受体1的概念。
成纤维细胞生长因子受体1 (FGFR1)在各种癌症的进展中起着至关重要的作用,参与细胞增殖、存活和分化的过程。FGFR1在免疫检查点抑制剂(ICIs)如派姆单抗和纳武单抗的耐药性中发挥作用。因此,使用单克隆抗体和酪氨酸激酶抑制剂靶向FGFR1并通过改变肿瘤微环境和对抗免疫抑制来增强ICIs是一种潜在的治疗策略。基于FGFR1相关研究和主动靶向策略,我们认为用抗FGFR1抗体修饰纳米药物表面(如OM-RCA-01)是一种有效的靶向治疗FGFR1高表达肿瘤的方法。虽然有相关研究证实了该方法的可行性,但在临床应用中存在挑战,特别是在大规模生产过程中如何保持统一的质量。因此,我们建议在未来进行进一步的优化研究,以加快此类给药系统的临床应用,为肿瘤治疗提供更高效、更具成本效益的选择。
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来源期刊
CiteScore
2.80
自引率
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审稿时长
13 weeks
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