Ait-Belkacem Rima, Berenguer Caroline, Villard Claude, Ouafik L'Houcine, Figarella-Branger Dominique, Beck Alain, Chinot Olivier, Lafitte Daniel
a Aix-Marseille Université Inserm ; CRO2 UMR S-911; Marseille , France.
MAbs. 2014;6(6):1385-93. doi: 10.4161/mabs.34405.
Bevacizumab induces normalization of abnormal blood vessels, making them less leaky. By binding to vascular endothelial growth factor, it indirectly attacks the vascular tumor mass. The optimal delivery of targeted therapies including monoclonal antibodies or anti-angiogenesis drugs to the target tissue highly depends on the blood-brain barrier permeability. It is therefore critical to investigate how drugs effectively reach the tumor. In situ investigation of drug distribution could provide a better understanding of pharmacological agent action and optimize chemotherapies for solid tumors. We developed an imaging method coupled to protein identification using matrix-assisted laser desorption/ionization mass spectrometry. This approach monitored bevacizumab distribution within the brain structures, and especially within the tumor, without any labeling.
贝伐单抗可使异常血管正常化,减少其渗漏。通过与血管内皮生长因子结合,它间接攻击血管肿瘤团块。包括单克隆抗体或抗血管生成药物在内的靶向治疗药物向靶组织的最佳递送高度依赖于血脑屏障的通透性。因此,研究药物如何有效到达肿瘤至关重要。药物分布的原位研究可以更好地理解药理作用,并优化实体瘤的化疗方案。我们开发了一种结合基质辅助激光解吸/电离质谱进行蛋白质鉴定的成像方法。这种方法可监测贝伐单抗在脑结构内,尤其是肿瘤内的分布,且无需任何标记。