Department of Cutaneous Oncology, Moffitt Cancer Center Tampa, FL 33612, United States.
Department of Cutaneous Oncology, Moffitt Cancer Center Tampa, FL 33612, United States.
Biochim Biophys Acta Rev Cancer. 2017 Dec;1868(2):500-509. doi: 10.1016/j.bbcan.2017.09.005. Epub 2017 Sep 27.
Nitric oxide (NO) is a small gaseous signaling molecule that mediates its effects in melanoma through free radical formation and enzymatic processes. Investigations have demonstrated multiple roles for NO in melanoma pathology via immune surveillance, apoptosis, angiogenesis, melanogenesis, and on the melanoma cell itself. In general, elevated levels of NO prognosticate a poor outcome for melanoma patients. However, there are processes where the relative concentration of NO in different environments may also serve to limit melanoma proliferation. This review serves to outline the roles of NO in melanoma development and proliferation. As demonstrated by multiple in vivo murine models and observations from human tissue, NO may promote melanoma formation and proliferation through its interaction via inhibitory immune cells, inhibition of apoptosis, stimulation of pro-tumorigenic cytokines, activation of tumor associated macrophages, alteration of angiogenic processes, and stimulation of melanoma formation itself.
一氧化氮(NO)是一种小的气体信号分子,通过自由基形成和酶促过程在黑色素瘤中发挥作用。研究表明,NO 通过免疫监视、细胞凋亡、血管生成、黑色素生成以及黑色素瘤细胞本身在黑色素瘤发病机制中发挥多种作用。一般来说,NO 水平升高预示黑色素瘤患者预后不良。然而,在某些情况下,不同环境中 NO 的相对浓度也可能限制黑色素瘤的增殖。本综述旨在概述 NO 在黑色素瘤发生和增殖中的作用。多项体内小鼠模型和人类组织观察表明,NO 可能通过与抑制性免疫细胞相互作用、抑制细胞凋亡、刺激促肿瘤细胞因子、激活肿瘤相关巨噬细胞、改变血管生成过程以及刺激黑色素瘤形成本身,从而促进黑色素瘤的形成和增殖。