Signaling crosstalk between tumor endothelial cells and immune cells in the microenvironment of solid tumors

Yuexin Xu, Chris P. Miller, S. Tykodi, S. Akilesh, E. Warren
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Abstract

Tumor-associated endothelial cells (TECs) are crucial mediators of immune surveillance and immune escape in the tumor microenvironment (TME). TECs driven by angiogenic growth factors form an abnormal vasculature which deploys molecular machinery to selectively promote the function and recruitment of immunosuppressive cells while simultaneously blocking the entry and function of anti-tumor immune cells. TECs also utilize a similar set of signaling regulators to promote the metastasis of tumor cells. Meanwhile, the tumor-infiltrating immune cells further induce the TEC anergy by secreting pro-angiogenic factors and prevents further immune cell penetration into the TME. Understanding the complex interactions between TECs and immune cells will be needed to successfully treat cancer patients with combined therapy to achieve vasculature normalization while augmenting antitumor immunity. In this review, we will discuss what is known about the signaling crosstalk between TECs and tumor-infiltrating immune cells to reveal insights and strategies for therapeutic targeting.
实体瘤微环境中肿瘤内皮细胞与免疫细胞之间的信号串扰
肿瘤相关内皮细胞(TEC)是肿瘤微环境(TME)中免疫监视和免疫逃逸的关键介质。TECs在血管生成生长因子的驱动下形成异常的血管,其分子机制可选择性地促进免疫抑制细胞的功能和招募,同时阻断抗肿瘤免疫细胞的进入和功能。TECs 还利用一套类似的信号调节器来促进肿瘤细胞的转移。同时,肿瘤浸润免疫细胞通过分泌促血管生成因子进一步诱导 TEC 失能,并阻止免疫细胞进一步渗透到 TME 中。要想成功地对癌症患者进行联合治疗,在增强抗肿瘤免疫力的同时实现血管正常化,就必须了解 TEC 与免疫细胞之间复杂的相互作用。在这篇综述中,我们将讨论目前已知的 TEC 与肿瘤浸润免疫细胞之间的信号串扰,以揭示治疗靶点的见解和策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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