Sharjah Institute for Medical Research, University of Sharjah, Sharjah, United Arab Emirates.
Department of Medical, Surgical, and Experimental Surgery, University of Sassari, Viale San Pietro 43,07100 Sassari, Italy.
Curr Pharm Des. 2021;27(18):2156-2169. doi: 10.2174/1381612827666210303143442.
Long-lasting subclinical inflammation is associated with a wide range of human diseases, particularly at a middle and older age. Recent reports showed that there is a direct causal link between inflammation and cancer development, as several cancers were found to be associated with chronic inflammatory conditions. In patients with cancer, healthy endothelial cells regulate vascular homeostasis, and it is believed that they can limit tumor growth, invasiveness, and metastasis. Conversely, dysfunctional endothelial cells that have been exposed to the inflammatory tumor microenvironment can support cancer progression and metastasis. Dysfunctional endothelial cells can exert these effects via diverse mechanisms, including dysregulated adhesion, permeability, and activation of NF-κB and STAT3 signaling. In this review, we highlight the role of vascular inflammation in predisposition to cancer within the context of two common disease risk factors: obesity and smoking. In addition, we discuss the molecular triggers, pathophysiological mechanisms, and the biological consequences of vascular inflammation during cancer development and metastasis. Finally, we summarize the current therapies and pharmacological agents that target vascular inflammation and endothelial dysfunction.
长期亚临床炎症与多种人类疾病有关,尤其是在中年和老年时期。最近的报告表明,炎症与癌症的发展之间存在直接的因果关系,因为几种癌症被发现与慢性炎症状态有关。在癌症患者中,健康的内皮细胞调节血管的稳态,并且人们认为它们可以限制肿瘤的生长、侵袭和转移。相反,暴露于炎症肿瘤微环境中的功能失调的内皮细胞可以支持癌症的进展和转移。功能失调的内皮细胞可以通过多种机制发挥这些作用,包括 NF-κB 和 STAT3 信号的失调黏附、通透性和激活。在这篇综述中,我们强调了血管炎症在肥胖和吸烟这两个常见疾病风险因素背景下导致癌症的作用。此外,我们还讨论了癌症发展和转移过程中血管炎症的分子触发因素、病理生理机制和生物学后果。最后,我们总结了目前针对血管炎症和内皮功能障碍的治疗方法和药理学制剂。