Forster Jake C, Harriss-Phillips Wendy M, Douglass Michael Jj, Bezak Eva
Department of Physics, University of Adelaide.
Department of Medical Physics, Royal Adelaide Hospital.
Hypoxia (Auckl). 2017 Apr 11;5:21-32. doi: 10.2147/HP.S133231. eCollection 2017.
The imbalance of angiogenic regulators in tumors drives tumor angiogenesis and causes the vasculature to develop much differently in tumors than in normal tissue. There are several cancer therapy techniques currently being used and developed that target the tumor vasculature for the treatment of solid tumors. This article reviews the aspects of the tumor vasculature that are relevant to most cancer therapies but particularly to vascular targeting techniques.
We conducted a review of identified experiments in which tumors were transplanted into animals to study the development of the tumor vasculature with tumor growth. Quantitative vasculature morphology data for spontaneous human head and neck cancers are reviewed. Parameters assessed include the highest microvascular density (h-MVD) and the relative vascular volume (RVV). The effects of the vasculature on the tumor microenvironment are discussed, including the distributions of hypoxia and proliferation.
Data for the h-MVD and RVV in head and neck cancers are highly varied, partly due to methodological differences. However, it is clear that the cancers are typically more vascularized than the corresponding normal tissue. The commonly observed chronic hypoxia and acute hypoxia in these tumors are due to high intratumor heterogeneity in MVD and lower than normal blood oxygenation levels through the abnormally developed tumor vasculature. Hypoxic regions are associated with decreased cell proliferation.
The morphology of the vasculature strongly influences the tumor microenvironment, with important implications for tumor response to medical intervention such as radiotherapy. Quantitative vasculature morphology data herein may be used to inform computational models that simulate the spatial tumor vasculature. Such models may play an important role in exploring and optimizing vascular targeting cancer therapies.
肿瘤中血管生成调节因子的失衡驱动肿瘤血管生成,并导致肿瘤血管系统的发育与正常组织有很大不同。目前正在使用和研发几种针对肿瘤血管系统来治疗实体瘤的癌症治疗技术。本文综述了与大多数癌症治疗相关,尤其是与血管靶向技术相关的肿瘤血管系统的各个方面。
我们对已确定的实验进行了综述,这些实验将肿瘤移植到动物体内以研究肿瘤血管系统随肿瘤生长的发育情况。回顾了自发性人类头颈癌的定量血管形态学数据。评估的参数包括最高微血管密度(h-MVD)和相对血管体积(RVV)。讨论了血管系统对肿瘤微环境的影响,包括缺氧和增殖的分布。
头颈癌中h-MVD和RVV的数据差异很大,部分原因是方法学上的差异。然而,很明显癌症通常比相应的正常组织血管化程度更高。这些肿瘤中常见的慢性缺氧和急性缺氧是由于MVD的肿瘤内高度异质性以及通过异常发育的肿瘤血管系统导致的低于正常的血液氧合水平。缺氧区域与细胞增殖减少有关。
血管系统的形态强烈影响肿瘤微环境,对诸如放射治疗等医学干预的肿瘤反应具有重要意义。本文中的定量血管形态学数据可用于为模拟肿瘤血管空间的计算模型提供信息。此类模型可能在探索和优化血管靶向癌症治疗中发挥重要作用。