Prostate Cancer Institute, National University of Ireland Galway, Dublin, Ireland.
Carcinogenesis. 2013 Mar;34(3):503-12. doi: 10.1093/carcin/bgt034. Epub 2013 Jan 25.
Nitric oxide (NO) is a short-lived, pleiotropic molecule that affects numerous critical functions in the body. Presently, there are markedly conflicting findings in the literature regarding NO and its role in carcinogenesis and tumor progression. NO has been shown to have dichotomous effects on cellular proliferation, apoptosis, migration, invasion, angiogenesis and many other important processes in cancer biology. It has been shown to be both pro- and antitumorigenic, depending on the concentration and the tumor microenvironment in question. NO is generated by three isoforms of NO synthase (NOS) that are widely expressed and sometimes upregulated in human tumors. Due to its vast array of physiological functions, it presents a huge challenge to researchers to discover its true potential in cancer biology and consequently, its use in anticancer therapies. In this study, we review the current knowledge in this area, with an emphasis placed on NO modulation as an anticancer therapy, focusing on NO-donating drugs and NOS inhibitors.
一氧化氮(NO)是一种短寿命、多功能的分子,影响着体内许多关键功能。目前,文献中关于 NO 及其在致癌和肿瘤进展中的作用存在明显的矛盾发现。NO 对细胞增殖、凋亡、迁移、侵袭、血管生成和癌症生物学中的许多其他重要过程具有双重作用。它被证明具有促癌和抑癌作用,具体取决于浓度和所涉及的肿瘤微环境。NO 由三种广泛表达且在人类肿瘤中有时上调的一氧化氮合酶(NOS)同工型生成。由于其广泛的生理功能,研究人员在发现其在癌症生物学中的真正潜力以及随后在抗癌治疗中的应用方面面临巨大挑战。在这项研究中,我们回顾了这一领域的现有知识,重点介绍了作为抗癌疗法的 NO 调节,侧重于一氧化氮供体药物和 NOS 抑制剂。