肿瘤抗血管生成治疗的耐药机制。

Q3 Medicine
遗传 Pub Date : 2024-11-01 DOI:10.16288/j.yczz.24-110
Xu Yan, Ying Guo, Dong-Lin Sun, Nan Wu, Yan Jin
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引用次数: 0

摘要

血管生成是指通过内皮细胞的迁移、增殖和分化,在原有血管的基础上形成新的血管网络的过程。这一过程对实体瘤的生长和扩散至关重要,尤其是当肿瘤体积超过 2 立方毫米时,因为新形成的血管网络可为肿瘤提供必需的氧气、营养物质和生长因子。抗血管生成疗法已成为临床上常用的癌症靶向治疗方法之一。贝伐单抗作为首个抗血管生成药物,已广泛应用于各种实体瘤的治疗。然而,由于存在获得性耐药性,其疗效通常只能维持 1 到 2 年。尽管内皮细胞的基因组相对稳定,不易产生耐药性,但在临床实践中还是观察到了各种类型的耐药现象,这表明抗血管生成治疗的耐药性仍然是一个具有挑战性的研究领域。本综述重点探讨肿瘤抗血管生成治疗耐药机制的最新进展,探索抗肿瘤血管生成治疗的新前景,以期为临床实践提供有力的理论支持和指导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Drug resistance mechanism of anti-angiogenesis therapy in tumor.

Angiogenesis refers to the process of forming a new network of blood vessels from existing ones through the migration, proliferation, and differentiation of endothelial cells. This process is crucial for the growth and spread of solid tumors, particularly once the tumor volume exceeds 2 mm3, as the newly formed vascular network provides essential oxygen, nutrients, and growth factors to the tumor. Anti-angiogenesis therapy has become one of the commonly used targeted treatments for cancer in clinical practice. Bevacizumab, the first anti-angiogenesis drug, has been widely applied in the treatment of various solid tumors. However, due to acquired resistance, its efficacy is typically sustained for only 1 to 2 years. Despite the relative genomic stability of endothelial cells, which makes resistance less likely, various types of resistance phenomena have been observed in clinical practice, indicating that resistance to anti-angiogenic therapy remains a challenging research area. This review focuses on the latest advances in the mechanisms of resistance to anti-angiogenic therapy in tumors and explores new prospects for anti-tumor angiogenesis treatment, in order to provide strong theoretical support and guidance for clinical practice.

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来源期刊
遗传
遗传 Medicine-Medicine (all)
CiteScore
2.50
自引率
0.00%
发文量
6699
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