Lee Shiuan-Shinn, Yang Shun-Fa, Ho Yung-Chuan, Tsai Chung-Hung, Chang Yu-Chao
Institute of Medicine, Chung Shan Medical University, Taichung, Taiwan.
Oral Oncol. 2008 Feb;44(2):180-6. doi: 10.1016/j.oraloncology.2007.01.019. Epub 2007 Apr 5.
Metallothioneins (MTs) are a family of low molecular weight, cysteine-rich, inducible, intracellular proteins that bind heavy metals with high affinity. MT-1 is known as a stress-inducible protein and functions as an antioxidant enzyme. Areca quid chewing is a major risk factor in the development and further progression of oral squamous cell carcinoma (OSCC). The aim of this study was to compare MT-1 expression in normal human oral epithelium and OSCC and further explore the potential mechanism that may lead to induce MT-1 expression. Thirty four OSCC and 10 normal epithelium specimens were examined by immunohistochemistry and analyzed by the clinico-pathological profiles. The oral epithelial cell line GMN cells were challenged with arecoline, a major areca nut alkaloid, by reverse-transcriptase polymerase chain reaction. Furthermore, tobacco smoke carcinogen benzo[a]pyrene (BaP) and glutathione (GSH) precursor N-acetyl-l-cysteine (NAC) were added to find the possible regulatory mechanisms. The results from immunohistochemistry demonstrated that MT-1 expression was significantly higher in OSCC specimens (p<0.05). No significant difference in MT-1 expression was observed with respect to age, sex, T category, and stage (p>0.05). The high MT-1 expression was associated with lymph node metastasis (p=0.012). In addition, arecoline was found to elevate MT-1 mRNA in a dose-dependent manner (p<0.05). Furthermore, the addition of BaP enhanced the arecoline-induced MT-1 expression (p<0.05). The addition of NAC markedly inhibited the arecoline-induced MT-1 expression (p<0.05). These results lead to the conclusion that MT-1 expression is significantly upregulated in areca quid chewing associated-OSCC. The expression profile suggests MT-1 could be used clinically as a marker for tumors possessing the potential for lymph node metastasis. The compounds of tobacco products may act synergistically in the pathogenesis of OSCC in areca quid chewers. The regulation of MT-1 expression induced by arecoline is critically dependent on the intracellular GSH concentration.
金属硫蛋白(MTs)是一类低分子量、富含半胱氨酸、可诱导的细胞内蛋白质家族,它们能与重金属高亲和力结合。MT-1是一种应激诱导蛋白,起抗氧化酶的作用。嚼槟榔是口腔鳞状细胞癌(OSCC)发生和进一步发展的主要危险因素。本研究的目的是比较MT-1在正常人口腔上皮和OSCC中的表达,并进一步探讨可能导致MT-1表达诱导的潜在机制。通过免疫组织化学检查34例OSCC和10例正常上皮标本,并根据临床病理特征进行分析。通过逆转录聚合酶链反应,用槟榔的主要生物碱槟榔碱刺激口腔上皮细胞系GMN细胞。此外,添加烟草烟雾致癌物苯并[a]芘(BaP)和谷胱甘肽(GSH)前体N-乙酰-L-半胱氨酸(NAC)以寻找可能的调节机制。免疫组织化学结果表明,MT-1在OSCC标本中的表达显著更高(p<0.05)。在年龄、性别、T分类和分期方面,MT-1表达未观察到显著差异(p>0.05)。MT-1高表达与淋巴结转移相关(p=0.012)。此外,发现槟榔碱以剂量依赖方式升高MT-1 mRNA(p<0.05)。此外,添加BaP增强了槟榔碱诱导的MT-1表达(p<0.05)。添加NAC显著抑制了槟榔碱诱导的MT-1表达(p<0.05)。这些结果得出结论,MT-1表达在嚼槟榔相关的OSCC中显著上调。表达谱表明MT-1可在临床上用作具有淋巴结转移潜能肿瘤的标志物。烟草制品的化合物可能在嚼槟榔者的OSCC发病机制中起协同作用。槟榔碱诱导的MT-1表达调节严重依赖于细胞内GSH浓度。