Gessi Stefania, Merighi Stefania, Sacchetto Valeria, Simioni Carolina, Borea Pier Andrea
Deaprtment of Clinical and Experimental Medicine, University of Ferrera, Ferrara, Italy.
Biochim Biophys Acta. 2011 May;1808(5):1400-12. doi: 10.1016/j.bbamem.2010.09.020. Epub 2010 Oct 1.
Adenosine is a ubiquitous signaling molecule whose physiological functions are mediated by its interaction with four G-protein-coupled receptor subtypes, termed A(1), A(2A), A(2B) and A(3). As a result of increased metabolic rates, this nucleoside is released from a variety of cells throughout the body in concentrations that can have a profound impact on vasculature and immunoescape. However, as high concentrations of adenosine have been reported in cancer tissues, it also appears to be implicated in the growth of tumors. Thus, full characterisation of the role of adenosine in tumor development, by addressing the question of whether adenosine receptors are present in cancer tissues, and, if so, which receptor subtype mediates its effects in cancer growth, is a vital research goal. To this end, this review focuses on the most relevant aspects of adenosine receptor subtype activation in tumors reported so far. Although all adenosine receptors now have an increasing number of recognised biological roles in tumors, it seems that the A(2A) and A(3) subtypes are the most promising as regards drug development. In particular, activation of A(2A) receptors leads to immunosuppressive effects, which decreases anti-tumoral immunity and thereby encourages tumor growth. Due to this behavior, the addition of A(2A) antagonists to cancer immunotherapeutic protocols has been suggested as a way of enhancing tumor immunotherapy. Interestingly, the safety of such compounds has already been demonstrated in trials employing A(2A) antagonists in the treatment of Parkinson's disease. As for A(3) receptors, the effectiveness of their agonists in several animal tumor models has led to the introduction of these molecules into a programme of pre-clinical and clinical trials. Paradoxically, A(3) receptor antagonists also appear to be promising candidates in human cancer treatment of regimes. Clearly, research in this still field is still in its infancy, with several important and challenging issues remaining to be addressed, although purine scientists do seem to be getting closer to their goal: the incorporation of adenosine ligands into drugs with the ability to save lives and improve human health.
腺苷是一种普遍存在的信号分子,其生理功能通过与四种G蛋白偶联受体亚型(称为A(1)、A(2A)、A(2B)和A(3))相互作用来介导。由于代谢率增加,这种核苷从全身各种细胞中释放出来,其浓度可对血管系统和免疫逃逸产生深远影响。然而,由于癌症组织中已报道存在高浓度的腺苷,它似乎也与肿瘤生长有关。因此,通过解决腺苷受体是否存在于癌症组织中以及如果存在,哪种受体亚型介导其在癌症生长中的作用这一问题,全面表征腺苷在肿瘤发展中的作用是一个至关重要的研究目标。为此,本综述聚焦于迄今报道的肿瘤中腺苷受体亚型激活的最相关方面。尽管现在所有腺苷受体在肿瘤中都有越来越多已被认可的生物学作用,但就药物开发而言,A(2A)和A(3)亚型似乎最具潜力。特别是,A(2A)受体的激活会导致免疫抑制作用,降低抗肿瘤免疫力,从而促进肿瘤生长。由于这种作用,有人建议在癌症免疫治疗方案中添加A(2A)拮抗剂,作为增强肿瘤免疫治疗的一种方法。有趣的是,此类化合物的安全性已在使用A(2A)拮抗剂治疗帕金森病的试验中得到证实。至于A(3)受体,其激动剂在几种动物肿瘤模型中的有效性已促使将这些分子引入临床前和临床试验计划。矛盾的是,A(3)受体拮抗剂在人类癌症治疗方案中似乎也是有前景的候选药物。显然,这个仍处于起步阶段的领域的研究仍有几个重要且具有挑战性的问题有待解决,尽管嘌呤科学家似乎确实正在接近他们的目标:将腺苷配体纳入能够挽救生命和改善人类健康的药物中。