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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。

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

作者信息

Xu Yuexin, Miller Chris P, Tykodi Scott S, Akilesh Shreeram, Warren Edus H

机构信息

Translational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA, United States.

Department of Medicine, Division of Hematology and Oncology, University of Washington, Seattle, WA, United States.

出版信息

Front Cell Dev Biol. 2024 Apr 25;12:1387198. doi: 10.3389/fcell.2024.1387198. eCollection 2024.

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.

摘要

肿瘤相关内皮细胞(TECs)是肿瘤微环境(TME)中免疫监视和免疫逃逸的关键介质。由血管生成生长因子驱动的TECs形成异常脉管系统,该系统利用分子机制选择性地促进免疫抑制细胞的功能和募集,同时阻断抗肿瘤免疫细胞的进入和功能。TECs还利用一组类似的信号调节因子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TECs无反应,并阻止免疫细胞进一步渗透到TME中。要成功地联合治疗癌症患者,实现脉管系统正常化并增强抗肿瘤免疫力,就需要了解TECs与免疫细胞之间的复杂相互作用。在这篇综述中,我们将讨论关于TECs与肿瘤浸润免疫细胞之间信号串扰的已知情况,以揭示治疗靶点的见解和策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9560/11079179/a5166093c36e/fcell-12-1387198-g001.jpg

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