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碱性成纤维细胞生长因子在癌症抗血管内皮生长因子治疗获得性耐药中的作用

Role of bFGF in Acquired Resistance upon Anti-VEGF Therapy in Cancer.

作者信息

Zahra Fatema Tuz, Sajib Md Sanaullah, Mikelis Constantinos M

机构信息

Department of Pharmaceutical Sciences, School of Pharmacy, Texas Tech University Health Sciences Center, Amarillo, TX 79106, USA.

出版信息

Cancers (Basel). 2021 Mar 20;13(6):1422. doi: 10.3390/cancers13061422.

Abstract

Anti-angiogenic approaches targeting the vascular endothelial growth factor (VEGF) signaling pathway have been a significant research focus during the past decades and are well established in clinical practice. Despite the expectations, their benefit is ephemeral in several diseases, including specific cancers. One of the most prominent side effects of the current, VEGF-based, anti-angiogenic treatments remains the development of resistance, mostly due to the upregulation and compensatory mechanisms of other growth factors, with the basic fibroblast growth factor (bFGF) being at the top of the list. Over the past decade, several anti-angiogenic approaches targeting simultaneously different growth factors and their signaling pathways have been developed and some have reached the clinical practice. In the present review, we summarize the knowledge regarding resistance mechanisms upon anti-angiogenic treatment, mainly focusing on bFGF. We discuss its role in acquired resistance upon prolonged anti-angiogenic treatment in different tumor settings, outline the reported resistance mechanisms leading to bFGF upregulation, and summarize the efforts and outcome of combined anti-angiogenic approaches to date.

摘要

在过去几十年中,针对血管内皮生长因子(VEGF)信号通路的抗血管生成方法一直是重要的研究热点,并且在临床实践中已得到充分确立。尽管寄予了厚望,但它们在包括特定癌症在内的几种疾病中的益处是短暂的。当前基于VEGF的抗血管生成治疗最突出的副作用之一仍然是耐药性的产生,这主要归因于其他生长因子的上调和补偿机制,其中碱性成纤维细胞生长因子(bFGF)位居榜首。在过去十年中,已经开发出几种同时针对不同生长因子及其信号通路的抗血管生成方法,其中一些已应用于临床实践。在本综述中,我们总结了有关抗血管生成治疗耐药机制的知识,主要聚焦于bFGF。我们讨论了它在不同肿瘤环境中长期抗血管生成治疗后获得性耐药中的作用,概述了导致bFGF上调的已报道耐药机制,并总结了迄今为止联合抗血管生成方法的研究成果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6882/8003808/7ee0a691c839/cancers-13-01422-g001.jpg

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