Xie Xiaoyan, Jiang Yuchen, Yuan Yao, Wang Peiqi, Li Xinyi, Chen Fangman, Sun Chongkui, Zhao Hang, Zeng Xin, Jiang Lu, Zhou Yu, Dan Hongxia, Feng Mingye, Liu Rui, Chen Qianming
State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu 610041, China.
Oncotarget. 2016 Sep 13;7(37):59987-60004. doi: 10.18632/oncotarget.11046.
Oral squamous cell carcinoma (OSCC) ranks among the most common cancer worldwide, and is associated with severe morbidity and high mortality. Oral submucous fibrosis (OSF), characterized by fibrosis of the mucosa of the upper digestive tract, is a pre-malignant lesion, but the molecular mechanisms underlying this malignant transformation remains to be elucidated. In this study, matrix-assisted laser desorption ionization imaging mass spectrometry (MALDI-IMS)-based proteomic strategy was employed to profile the differentially expressed peptides/proteins between OSCC tissues and the corresponding adjacent non-cancerous OSF tissues. Sixty-five unique peptide peaks and nine proteins were identified with altered expression levels. Of them, expression of NCOA7 was found to be up-regulated in OSCC tissues by immunohistochemistry staining and western blotting, and correlated with a pan of clinicopathologic parameters, including lesion site, tumor differentiation status and lymph node metastasis. Further, we show that overexpression of NCOA7 promotes OSCC cell proliferation in either in vitro or in vivo models. Mechanistic study demonstrates that NCOA7 induces OSCC cell proliferation probably by activating aryl hydrocarbon receptor (AHR). The present study suggests that NCOA7 is a potential biomarker for early diagnosis of OSF malignant transformation, and leads to a better understanding of the molecular mechanisms responsible for OSCC development.
口腔鳞状细胞癌(OSCC)是全球最常见的癌症之一,与严重的发病率和高死亡率相关。口腔黏膜下纤维化(OSF)以上消化道黏膜纤维化为特征,是一种癌前病变,但其恶性转化的分子机制仍有待阐明。在本研究中,采用基于基质辅助激光解吸电离成像质谱(MALDI-IMS)的蛋白质组学策略,对OSCC组织和相应的相邻非癌性OSF组织之间差异表达的肽段/蛋白质进行分析。共鉴定出65个独特的肽峰和9种表达水平改变的蛋白质。其中,通过免疫组织化学染色和蛋白质印迹法发现NCOA7在OSCC组织中的表达上调,且与包括病变部位、肿瘤分化状态和淋巴结转移在内的一系列临床病理参数相关。此外,我们发现NCOA7的过表达在体外或体内模型中均能促进OSCC细胞增殖。机制研究表明,NCOA7可能通过激活芳烃受体(AHR)诱导OSCC细胞增殖。本研究提示,NCOA7是OSF恶性转化早期诊断的潜在生物标志物,有助于更好地理解OSCC发生发展的分子机制。