Ribatti Domenico, Annese Tiziana, Ruggieri Simona, Tamma Roberto, Crivellato Enrico
Department of Basic Medical Sciences, Neurosciences and Sensory Organs, University of Bari Medical School, Bari, Italy.
Department of Basic Medical Sciences, Neurosciences and Sensory Organs, University of Bari Medical School, Bari, Italy.
Transl Oncol. 2019 Jul;12(7):981-986. doi: 10.1016/j.tranon.2019.04.022. Epub 2019 May 20.
Clinical trials using anti-vascular endothelial growth factor /(VEGF) molecules induce a modest improvement in overall survival, measurable in weeks to just a few months, and tumors respond differently to these agents. In this review article, we have exposed some tumor characteristics and processes that may impair the effectiveness of anti-angiogenic approaches, including genotypic changes on endothelial cells, the vascular normalization phenomenon, and the vasculogenic mimicry. The usage of anti-angiogenic molecules leads to hypoxic tumor microenvironment which enhances tumor invasiveness. The role of tumor-infiltrating cells, including tumor associated macrophages and fibroblasts (TAMs and TAFs) in the therapeutic response to anti-angiogenic settings was also highlighted. Finally, among the new therapeutic approaches to target tumor vasculature, anti-PD-1 or anti-PD-L1 therapy sensitizing and prolonging the efficacy of anti-angiogenic therapy, have been discussed.
使用抗血管内皮生长因子/(VEGF)分子的临床试验使总生存期有适度改善,可测量的时间为几周至短短几个月,并且肿瘤对这些药物的反应各不相同。在这篇综述文章中,我们揭示了一些可能损害抗血管生成方法有效性的肿瘤特征和过程,包括内皮细胞的基因型变化、血管正常化现象和血管生成拟态。抗血管生成分子的使用导致肿瘤缺氧微环境,从而增强肿瘤侵袭性。还强调了肿瘤浸润细胞,包括肿瘤相关巨噬细胞和成纤维细胞(TAM和TAF)在抗血管生成治疗反应中的作用。最后,在针对肿瘤血管系统的新治疗方法中,讨论了使抗血管生成治疗敏感并延长其疗效的抗PD-1或抗PD-L1治疗。