Laurenzana Anna, Fibbi Gabriella, Chillà Anastasia, Margheri Giancarlo, Del Rosso Tommaso, Rovida Elisabetta, Del Rosso Mario, Margheri Francesca
Section of Experimental Pathology and Oncology, Department of Experimental and Clinical Biomedical Sciences, University of Florence, Viale GB Morgagni 50, 50134, Florence, Italy.
Cell Mol Life Sci. 2015 Apr;72(8):1537-57. doi: 10.1007/s00018-014-1814-x. Epub 2015 Jan 1.
Research on the nanoscale membrane structures known as lipid rafts is relevant to the fields of cancer biology, inflammation and ischaemia. Lipid rafts recruit molecules critical to signalling and regulation of the invasion process in malignant cells, the leukocytes that provide immunity in inflammation and the endothelial cells that build blood and lymphatic vessels, as well as the patterning of neural networks. As angiogenesis is a common denominator, regulation of receptors and signalling molecules critical to angiogenesis is central to the design of new approaches aimed at reducing, promoting or normalizing the angiogenic process. The goal of this review is to highlight some of the key issues that indicate the involvement of endothelial cell lipid rafts at each step of so-called 'sprouting angiogenesis', from stimulation of the vascular endothelial growth factor to the choice of tip cells, activation of migratory and invasion pathways, recruitment of molecules that guide axons in vascular patterning and maturation of blood vessels. Finally, the review addresses opportunities for future studies to define how these lipid domains (and their constituents) may be manipulated to stimulate the so-called 'normalization' of vascular networks within tumors, and be identified as the main target, enabling the development of more efficient chemotherapeutics and cancer immunotherapies.
对被称为脂筏的纳米级膜结构的研究与癌症生物学、炎症和缺血等领域相关。脂筏招募对恶性细胞侵袭过程的信号传导和调节至关重要的分子,在炎症中提供免疫的白细胞,构建血管和淋巴管的内皮细胞,以及神经网络的形成。由于血管生成是一个共同因素,对血管生成至关重要的受体和信号分子的调节是旨在减少、促进或使血管生成过程正常化的新方法设计的核心。本综述的目的是强调一些关键问题,这些问题表明内皮细胞脂筏在所谓的“芽生血管生成”的每个步骤中都有参与,从血管内皮生长因子的刺激到顶端细胞的选择、迁移和侵袭途径的激活、在血管形成中引导轴突的分子的募集以及血管的成熟。最后,该综述探讨了未来研究的机会,以确定如何操纵这些脂质结构域(及其成分)来刺激肿瘤内血管网络的所谓“正常化”,并将其确定为主要靶点,从而开发出更有效的化疗药物和癌症免疫疗法。