Manoharan Vahinipriya, Adegbayi Oluwafemi O, Maynard Janielle P
Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Purinergic Signal. 2024 Oct 10. doi: 10.1007/s11302-024-10054-7.
P2 purinergic receptor expression is dysregulated in multiple cancer subtypes and is associated with worse outcomes. Studies identify roles for P2 purinergic receptors in tumor cells that drive disease aggressiveness. There is also sufficient evidence that P2 purinergic receptor expression within the tumor microenvironment (TME) is critical for disease initiation and progression. Immune cells constitute a significant component of the TME and display both tumorigenic and anti-tumorigenic potential. Studies pre-dating the investigation of P2 purinergic receptors in cancer identify P2 receptor expression on multiple immune cells including macrophages, neutrophils, T-cells, and dendritic cells; all of which are implicated in tumor initiation, tumor promotion, or response to treatment. Herein, we discuss P2 purinergic receptor expression and function in tumor-related immune cells. We provide a rationale for further investigations of P2 purinergic receptors within the TME to better define the mechanistic pathways of inflammation-mediate tumorigenesis and explore P2 purinergic receptors as potential targets for novel immunotherapeutic approaches.
P2嘌呤能受体在多种癌症亚型中表达失调,且与较差的预后相关。研究确定了P2嘌呤能受体在驱动疾病侵袭性的肿瘤细胞中的作用。也有充分证据表明,肿瘤微环境(TME)中的P2嘌呤能受体表达对疾病的起始和进展至关重要。免疫细胞是TME的重要组成部分,具有致瘤和抗肿瘤潜力。在癌症中对P2嘌呤能受体进行研究之前的研究确定,包括巨噬细胞、中性粒细胞、T细胞和树突状细胞在内的多种免疫细胞上存在P2受体表达;所有这些细胞都与肿瘤起始、肿瘤促进或对治疗的反应有关。在此,我们讨论P2嘌呤能受体在肿瘤相关免疫细胞中的表达和功能。我们为进一步研究TME中的P2嘌呤能受体提供了理论依据,以更好地定义炎症介导的肿瘤发生的机制途径,并探索将P2嘌呤能受体作为新型免疫治疗方法的潜在靶点。