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Natural Killer Cells as Key Players of Tumor Progression and Angiogenesis: Old and Novel Tools to Divert Their Pro-Tumor Activities into Potent Anti-Tumor Effects

机译:天然杀伤细胞作为肿瘤进展和血管生成的关键参与者:旧的和新颖的工具,将其促肿瘤活性转化为有效的抗肿瘤作用

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摘要

Immune cells, as a consequence of their plasticity, can acquire altered phenotype/functions within the tumor microenvironment (TME). Some of these aberrant functions include attenuation of targeting and killing of tumor cells, tolerogenic/immunosuppressive behavior and acquisition of pro-angiogenic activities. Natural killer (NK) cells are effector lymphocytes involved in tumor immunosurveillance. In solid malignancies, tumor-associated NK cells (TANK cells) in peripheral blood and tumor-infiltrating NK (TINK) cells show altered phenotypes and are characterized by either anergy or reduced cytotoxicity. Here, we aim at discussing how NK cells can support tumor progression and how induction of angiogenesis, due to TME stimuli, can be a relevant part on the NK cell-associated tumor supporting activities. We will review and discuss the contribution of the TME in shaping NK cell response favoring cancer progression. We will focus on TME-derived set of factors such as TGF-β, soluble HLA-G, prostaglandin E2, adenosine, extracellular vesicles, and miRNAs, which can exhibit a dual function. On one hand, these factors can suppress NK cell-mediated activities but, on the other hand, they can induce a pro-angiogenic polarization in NK cells. Also, we will analyze the impact on cancer progression of the interaction of NK cells with several TME-associated cells, including macrophages, neutrophils, mast cells, cancer-associated fibroblasts, and endothelial cells. Then, we will discuss the most relevant therapeutic approaches aimed at potentiating/restoring NK cell activities against tumors. Finally, supported by the literature revision and our new findings on NK cell pro-angiogenic activities, we uphold NK cells to a key host cellular paradigm in controlling tumor progression and angiogenesis; thus, we should bear in mind NK cells like a TME-associated target for anti-tumor therapeutic approaches.
机译:免疫细胞由于具有可塑性,可以在肿瘤微环境(TME)中获得改变的表型/功能。这些异常功能中的一些包括减弱对肿瘤细胞的靶向和杀死,耐受性/免疫抑制行为和促血管生成活性的获得。天然杀伤(NK)细胞是参与肿瘤免疫监测的效应淋巴细胞。在实体恶性肿瘤中,外周血中的肿瘤相关NK细胞(TANK细胞)和肿瘤浸润性NK(TINK)细胞表现出改变的表型,并以无反应性或降低的细胞毒性为特征。在这里,我们旨在讨论NK细胞如何支持肿瘤进展以及由于TME刺激引起的血管生成诱导如何成为与NK细胞相关的肿瘤支持活动的相关部分。我们将回顾和讨论TME在塑造有利于癌症进展的NK细胞反应中的作用。我们将重点关注TME衍生的一组因子,例如TGF-β,可溶性HLA-G,前列腺素E2,腺苷,细胞外囊泡和miRNA,它们可以显示双重功能。一方面,这些因素可以抑制NK细胞介导的活性,但另一方面,它们可以诱导NK细胞中促血管生成的极化。此外,我们将分析NK细胞与几种TME相关细胞(包括巨噬细胞,嗜中性粒细胞,肥大细胞,癌症相关成纤维细胞和内皮细胞)相互作用对癌症进展的影响。然后,我们将讨论旨在增强/恢复针对肿瘤的NK细胞活性的最相关的治疗方法。最后,在文献修订和我们对NK细胞促血管生成活性的新发现的支持下,我们将NK细胞坚持为控制肿瘤进程和血管生成的关键宿主细胞范例。因此,我们应该牢记NK细胞像TME相关的抗肿瘤治疗靶标。

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