CÚRAM, SFI Research Centre for Medical Devices, National University of Ireland Galway, Galway H91 W2TY, Ireland.
Discipline of Pathology, Lambe Institute for Translational Research, School of Medicine, National University of Ireland Galway, Galway H91 TK33, Ireland.
Biomacromolecules. 2022 Sep 12;23(9):3621-3647. doi: 10.1021/acs.biomac.2c00545. Epub 2022 Aug 3.
Nitric oxide (NO) is one of the prominent free radicals, playing a pivotal role in breast cancer progression. Hyaluronic acid (HA) plays an essential role in neutralizing free radicals in tumor tissues. However, its interactions with nitric oxide have not been thoroughly investigated. Hence, this study attempts to understand the mechanism of these interactions and the different effects on the intracellular NO levels and migration of breast cancer cells. The affinity of HA to scavenge NO was investigated alongside the accompanying changes in specific physico-chemical properties and the further effects on the NO-induced attachment and migration of the breast cancer cell lines, MDA-MB-231 and HCC1806. The reaction of the nitrogen dioxide radical, formed via NO/O interactions, with HA initiated a series of oxidative reactions, which, in the presence of NO, induce the fragmentation of the polymeric chains. Furthermore, these interactions were found to hinder the NO-induced migration of cancer cells. However, the NO-induced HA modification/fragmentation was inhibited in the presence of hemin, a NO-scavenging compound. Collectively, these results help toward understanding the involvement of HA in the NO-induced cell migration and suggest the possible modification of HA, used as one of the main materials in different biomedical applications.
一氧化氮(NO)是一种重要的自由基,在乳腺癌的进展中起着关键作用。透明质酸(HA)在中和肿瘤组织中的自由基方面起着至关重要的作用。然而,其与一氧化氮的相互作用尚未得到充分研究。因此,本研究试图了解这些相互作用的机制以及对乳腺癌细胞内 NO 水平和迁移的不同影响。研究了 HA 对 NO 的亲和力,以及伴随的特定物理化学性质的变化,以及对 NO 诱导的乳腺癌细胞系 MDA-MB-231 和 HCC1806 附着和迁移的进一步影响。NO/O 相互作用形成的二氧化氮自由基与 HA 反应引发了一系列氧化反应,在 NO 的存在下,诱导聚合物链的断裂。此外,这些相互作用被发现阻碍了 NO 诱导的癌细胞迁移。然而,在存在血红蛋白(一种清除 NO 的化合物)的情况下,NO 诱导的 HA 修饰/断裂被抑制。总的来说,这些结果有助于了解 HA 在 NO 诱导的细胞迁移中的作用,并提示可能对 HA 进行修饰,HA 作为不同生物医学应用中的主要材料之一。