Shang Z-J, Li Z-B, Li J-R
Key Laboratory of Oral Biomedical Engineering, Ministry of Education, School of Stomatology, Wuhan University, 237 Luoyu Road, Wuhan 430079, PR China.
Int J Oral Maxillofac Surg. 2006 Jun;35(6):539-43. doi: 10.1016/j.ijom.2006.01.004. Epub 2006 Feb 23.
It has been reported that increased nitric oxide synthase (NOS) expression and nitric oxide (NO) production may play an important role in cancer biology. The aim of this study was to determine the roles of NO in tumour cellular proliferation and DNA or RNA synthesis, and to investigate the therapeutic potential of NOS inhibitors in oral cancer. After exposure to different concentrations of the NOS inhibitor N(G)-nitro-L-arginine methyl ester (L-NAME), the growth of TSCCa cells, established from a patient with squamous cell carcinoma of the tongue, was evaluated using MTT and crystal violet assay. DNA or RNA synthesis, inducible/endothelial NOS (iNOS/eNOS) mRNA expression and NO production were then examined to determine the possible mechanisms of inhibitory effects of L-NAME on TSCCa cells. L-NAME had an inhibitory effect on TSCCa cell growth in both a concentration- and time-dependent manner. Acridine orange staining revealed that DNA and/or RNA synthesis of TSCCa cells was reduced after treatment with L-NAME. An in situ hybridisation (ISH) study showed clearly that L-NAME down-regulated eNOS and iNOS mRNA expression and this was followed by a decrease in NO production. It is postulated that the NOS/NO pathway may be implicated in cellular proliferation and DNA or RNA synthesis of cancer cells, apart from promoting tumour angiogenesis. Further studies have provided with new insight into the mechanisms by which NOS/NO takes part in oral carcinogenesis, and possible therapeutic interventions based on the NOS/NO pathway for tumour progression control.
据报道,一氧化氮合酶(NOS)表达增加和一氧化氮(NO)生成增多可能在癌症生物学中发挥重要作用。本研究的目的是确定NO在肿瘤细胞增殖以及DNA或RNA合成中的作用,并研究NOS抑制剂在口腔癌中的治疗潜力。在用不同浓度的NOS抑制剂N(G)-硝基-L-精氨酸甲酯(L-NAME)处理后,使用MTT和结晶紫测定法评估从一名舌鳞状细胞癌患者建立的TSCCa细胞的生长情况。然后检测DNA或RNA合成、诱导型/内皮型NOS(iNOS/eNOS)mRNA表达和NO生成,以确定L-NAME对TSCCa细胞抑制作用的可能机制。L-NAME对TSCCa细胞生长具有浓度和时间依赖性抑制作用。吖啶橙染色显示,用L-NAME处理后,TSCCa细胞的DNA和/或RNA合成减少。原位杂交(ISH)研究清楚地表明,L-NAME下调了eNOS和iNOS mRNA表达,随后NO生成减少。据推测,除了促进肿瘤血管生成外,NOS/NO途径可能与癌细胞的细胞增殖以及DNA或RNA合成有关。进一步的研究为NOS/NO参与口腔癌发生的机制以及基于NOS/NO途径控制肿瘤进展的可能治疗干预提供了新的见解。