Tumour vessel remodelling: new opportunities in cancer treatment.

Vascular biology (Bristol, England) Pub Date : 2020-01-14 eCollection Date: 2020-01-01 DOI:10.1530/VB-19-0032
Ruth Ganss
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引用次数: 16

Abstract

Tumour growth critically depends on a supportive microenvironment, including the tumour vasculature. Tumour blood vessels are structurally abnormal and functionally anergic which limits drug access and immune responses in solid cancers. Thus, tumour vasculature has been considered an attractive therapeutic target for decades. However, with time, anti-angiogenic therapy has evolved from destruction to structural and functional rehabilitation as understanding of tumour vascular biology became more refined. Vessel remodelling or normalisation strategies which alleviate hypoxia are now coming of age having been shown to have profound effects on the tumour microenvironment. This includes improved tumour perfusion, release from immune suppression and lower metastasis rates. Nevertheless, clinical translation has been slow due to challenges such as the transient nature of current normalisation strategies, limited in vivo monitoring and the heterogeneity of primary and/or metastatic tumour environments, calling for more tailored approaches to vascular remodelling. Despite these setbacks, harnessing vascular plasticity provides unique opportunities for anti-cancer combination therapies in particular anti-angiogenic immunotherapy which are yet to reach their full potential.

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肿瘤血管重塑:癌症治疗的新机遇。
肿瘤的生长严重依赖于一个支持性的微环境,包括肿瘤的血管系统。肿瘤血管在结构上异常,功能上无能,这限制了实体癌的药物通路和免疫反应。因此,几十年来,肿瘤血管系统一直被认为是一个有吸引力的治疗靶点。然而,随着时间的推移,随着对肿瘤血管生物学的理解更加完善,抗血管生成治疗已经从破坏发展到结构和功能康复。缓解缺氧的血管重塑或正常化策略现已成熟,已被证明对肿瘤微环境有深远的影响。这包括改善肿瘤灌注,释放免疫抑制和降低转移率。然而,由于当前正常化策略的短暂性、有限的体内监测以及原发性和/或转移性肿瘤环境的异质性等挑战,临床转化一直很慢,这需要更有针对性的血管重构方法。尽管有这些挫折,利用血管可塑性为抗癌联合疗法提供了独特的机会,特别是抗血管生成免疫疗法,尚未充分发挥其潜力。
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