未来展望:以成纤维细胞生长因子受体1为靶点,提高免疫治疗效果。

Q3 Medicine
Exploration of targeted anti-tumor therapy Pub Date : 2025-06-20 eCollection Date: 2025-01-01 DOI:10.37349/etat.2025.1002327
Ilya Tsimafeyeu
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引用次数: 0

摘要

成纤维细胞生长因子受体1 (FGFR1)通过参与细胞增殖、存活和分化,在各种癌症的进展中起着关键作用。最近,FGFR1与免疫逃避机制有关,特别是其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的作用。用单克隆抗体和酪氨酸激酶抑制剂靶向FGFR1已成为一种有希望的治疗策略,通过改变肿瘤微环境和对抗免疫抑制来增强ICI疗效。临床前研究表明,FGFR1抑制剂(如新型单克隆抗体OM-RCA-01)与ICIs联合使用可显著提高抗肿瘤活性,增强T细胞反应和细胞因子的产生。本文探讨了FGFR1在癌症生物学中的作用,它对免疫治疗耐药性的贡献,以及靶向FGFR1增强ICIs疗效的治疗潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Future perspectives: targeting fibroblast growth factor receptor 1 to enhance the efficacy of immunotherapy.

Fibroblast growth factor receptor 1 (FGFR1) plays a critical role in the progression of various cancers through its involvement in cell proliferation, survival, and differentiation. More recently, FGFR1 has been implicated in the mechanisms of immune evasion, particularly its role in resistance to immune checkpoint inhibitors (ICIs) such as pembrolizumab and nivolumab. Targeting FGFR1 with monoclonal antibodies and tyrosine kinase inhibitors has emerged as a promising therapeutic strategy to enhance ICI efficacy by altering the tumor microenvironment and countering immune suppression. Preclinical studies demonstrate that combining FGFR1 inhibitors, such as the novel monoclonal antibody OM-RCA-01, with ICIs significantly improves antitumor activity, enhancing T cell responses and cytokine production. This article explores the role of FGFR1 in cancer biology, its contribution to immunotherapy resistance, and the therapeutic potential of targeting FGFR1 to enhance the efficacy of ICIs.

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来源期刊
CiteScore
2.80
自引率
0.00%
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审稿时长
13 weeks
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