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成纤维细胞生长因子受体靶向治疗获得性耐药的机制

Mechanisms of acquired resistance to fibroblast growth factor receptor targeted therapy.

作者信息

Lau David K, Jenkins Laura, Weickhardt Andrew

机构信息

Olivia Newton John Cancer Research Institute, Heidelberg, Victoria 3084, Australia.

School of Cancer Medicine, La Trobe University, Heidelberg, Victoria 3084, Australia.

出版信息

Cancer Drug Resist. 2019 Sep 19;2(3):568-579. doi: 10.20517/cdr.2019.42. eCollection 2019.

Abstract

Oncogenic activation of the fibroblast growth factor receptor (FGFR) through mutations and fusions of the gene occur in a variety of different malignancies such as urothelial carcinoma and cholangiocarcinoma. Inhibition of the kinase domain of the FGFR with targeted oral FGFR inhibitors has been shown in both preclinical and early phase clinical trials to lead to meaningful reductions in tumour size and larger confirmatory randomized trials are underway. Acquired resistance to FGFR inhibition using a variety of mechanisms that includes, activation of alternate signaling pathways and expansion of tumour clones with gatekeeper mutations in the gene. This review summarizes the acquired resistance mechanisms to FGFR therapy and therapeutic approaches to circumventing resistance.

摘要

成纤维细胞生长因子受体(FGFR)基因通过突变和融合发生致癌激活,见于多种不同的恶性肿瘤,如尿路上皮癌和胆管癌。在临床前和早期临床试验中均已表明,使用靶向口服FGFR抑制剂抑制FGFR的激酶结构域可使肿瘤大小显著减小,目前正在进行更大规模的验证性随机试验。通过多种机制获得对FGFR抑制的耐药性,这些机制包括激活替代信号通路以及具有该基因守门人突变的肿瘤克隆的扩增。本综述总结了FGFR治疗的获得性耐药机制以及规避耐药性的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/251d/8992533/48dab0942ba5/cdr-2-568.fig.1.jpg

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