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Overexpression of nicotinamide N-methyltransferase in HSC-2 OSCC cell line: effect on apoptosis and cell proliferation

机译:HSC-2 OSCC细胞系中烟酰胺N-甲基转移酶的过度表达:对凋亡和细胞增殖的影响

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ObjectivesOral squamous cell carcinoma (OSCC) is the most common malignancy of oral cavity. Despite advances in therapeutic approaches, the 5-year survival rate for oral cancer has not improved in the last three decades. Therefore, new molecular targets for early diagnosis and treatment of OSCC are needed. In the present study, we focused on the enzyme nicotinamide N-methyltransferase (NNMT). We have previously shown that enzyme expression is upregulated in OSCC and NNMT knockdown in PE/CA PJ-15 cells significantly decreased cell growth in vitro and tumorigenicity in vivo.Material and methodsTo further explore the role of the enzyme in oral cancer cell metabolism, HSC-2 cells were transfected with the NNMT expression vector (pcDNA3-NNMT) and the effect of enzyme upregulation on cell proliferation was evaluated by MTT assay. Subsequently, we investigated at molecular level the role of NNMT on apoptosis and cell proliferation, by exploring the expression of -catenin, survivin, and Ki-67 by real-time PCR. Moreover, we performed immunohistochemistry on 20 OSCC tissue samples to explore the expression level of NNMT and survivin Ex3 isoform.ResultsEnzyme upregulation significantly increased cell growth in vitro. Moreover, a positive correlation between NNMT and survivin Ex3 isoform expression levels was found both in HSC-2 cells and in OSCC tissue samples.ConclusionTaken together, our results indicate a possible involvement of NNMT in the proliferation and tumorigenic capacity of OSCC cells and seem to suggest that the enzyme could represent a potential target for the treatment of oral cancer.Clinical relevanceThe involvement of NNMT in cell growth and anti-apoptotic mechanisms seems to suggest that this enzyme could be a new therapeutic target to improve the survival of OSCC patients.
机译:Objective Oral鳞状细胞癌(OSCC)是口腔最常见的恶性肿瘤。尽管治疗方法有所进展,但在过去三十年中,口腔癌的5年生存率尚未得到改善。因此,需要新的诊断和治疗OSCC的新分子靶标。在本研究中,我们专注于酶烟酰胺N-甲基转移酶(NNMT)。我们之前已经表明,酶表达在OSCC中上调,PE / Ca PJ-15细胞中的NNMT敲低在体外,体外细胞生长显着降低,体外致致瘤性的方法。材料和方法进一步探讨了酶在口腔癌细胞代谢中的作用,HSC用NNMT表达载体(PCDNA3-NNMT)转染-2细胞,并通过MTT测定评估酶上调对细胞增殖的影响。随后,我们通过分子水平研究NNMT在通过实时PCR探索-Catenin,Survivin和Ki-67的表达来对细胞凋亡和细胞增殖的作用。此外,我们在20个OSCC组织样品上进行免疫组织化学,以探讨NNMT和Survivin EX3同种型的表达水平。细胞酶上调显着提高了体外细胞生长。此外,在HSC-2细胞和OSCC组织样品中发现NNMT和Survivin EX3同种型表达水平的正相关性。结合在一起,我们的结果表明NNMT在OSCC细胞增殖和致瘤能力中的可能涉及似乎建议酶可以代表治疗口腔癌的潜在目标。临床相关性NNMT在细胞生长和抗凋亡机制中的涉及似乎表明该酶可以是改善OSCC患者存活的新治疗靶标。

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