Martin John D, Fukumura Dai, Duda Dan G, Boucher Yves, Jain Rakesh K
Edwin L. Steele Laboratories, Department of Radiation Oncology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts 02114.
Cold Spring Harb Perspect Med. 2016 Dec 1;6(12):a027094. doi: 10.1101/cshperspect.a027094.
Solid tumors consist of cancer cells and stromal cells, including resident and transiting immune cells-all ensconced in an extracellular matrix (ECM)-nourished by blood vessels and drained by lymphatic vessels. The microenvironment constituents are abnormal and heterogeneous in morphology, phenotype, and physiology. Such irregularities include an inefficient tumor vascular network comprised of leaky and compressed vessels, which impair blood flow and oxygen delivery. Low oxygenation in certain tumor regions-or focal hypoxia-is a mediator of cancer progression, metastasis, immunosuppression, and treatment resistance. Thus, repairing an abnormal and heterogeneous microenvironment-and hypoxia in particular-can significantly improve treatments of solid tumors. Here, we summarize two strategies to reengineer the tumor microenvironment (TME)-vessel normalization and decompression-that can alleviate hypoxia. In addition, we discuss how these two strategies alone and in combination with each other-or other therapeutic strategies-may overcome the challenges posed by cancer heterogeneity.
实体瘤由癌细胞和基质细胞组成,包括驻留和游走的免疫细胞,所有这些细胞都包裹在由血管滋养、淋巴管引流的细胞外基质(ECM)中。微环境成分在形态、表型和生理学方面是异常且异质性的。这些异常包括由渗漏和受压血管组成的低效肿瘤血管网络,这会损害血流和氧气输送。某些肿瘤区域的低氧状态——即局部缺氧——是癌症进展、转移、免疫抑制和治疗抵抗的介导因素。因此,修复异常且异质性的微环境——尤其是缺氧状态——可以显著改善实体瘤的治疗效果。在此,我们总结了两种重新构建肿瘤微环境(TME)的策略——血管正常化和减压,这两种策略可以缓解缺氧。此外,我们还讨论了这两种策略单独使用、相互结合或与其他治疗策略联合使用时,如何克服癌症异质性带来的挑战。