对Bit1作为食管鳞状细胞癌和腺癌潜在生物标志物的初步评估。
Preliminary evaluation for Bit1 as a potential biomarker for squamous cell carcinoma and adenocarcinoma of esophagus.
作者信息
Chen Jing, Liu Hongtao, Gao Pan, Hui Yiran, Yang Zhenzhen, Zhang Xiaqing, Xu Peirong, Tian Fang, Fan Tianli
机构信息
1 Department of Oncology, The Zhengzhou Central Hospital Affiliated to Zhengzhou University, Zhengzhou, China.
2 Department of Pharmacology, School of Basic Medicine, Zhengzhou University, Zhengzhou, China.
出版信息
Tumour Biol. 2017 May;39(5):1010428317708267. doi: 10.1177/1010428317708267.
Mounting evidence has demonstrated that Bit1 has been investigated as an etiological factor for certain cancers, including esophageal squamous cell carcinoma reported in our previous study, but data regarding possible roles of Bit1 in esophageal squamous cell carcinoma and esophageal adenocarcinoma remain to be elucidated. The purpose of this study was to examine whether Bit1 can be a novel diagnostic marker for the patients with esophageal squamous cell carcinoma and esophageal adenocarcinoma. The results revealed that Bit1 level in esophageal squamous cell carcinoma was significantly higher than that in esophageal adenocarcinoma tissues ( p < 0.05); notably, Bit1 level in esophageal adenocarcinoma tissues was lower than that in paired normal tissues but no difference was found ( p > 0.05). Bit1 expression patterns were completely in accordance with matrix metalloproteinase 2 and Bcl-2 in esophageal squamous cell carcinoma and esophageal adenocarcinoma. In addition, Bit1, Bcl-2, and matrix metalloproteinase 2 expression patterns in different differentiated esophageal squamous cell carcinoma were higher than those in corresponding normal esophageal tissues. Bit1 expression in poorly differentiated esophageal squamous cell carcinoma was significantly higher than that in normal esophageal tissues ( p < 0.05) but not in moderately and well-differentiated esophageal squamous cell carcinoma. Matrix metalloproteinase 2 expression patterns in poorly and moderately differentiated esophageal squamous cell carcinoma were significantly higher than those in corresponding normal esophageal tissues ( p < 0.01) but not in well-differentiated esophageal squamous cell carcinoma tissue ( p > 0.05). Bcl-2 expression patterns in various differentiated esophageal squamous cell carcinoma were higher than those in corresponding normal esophageal tissues with no statistical differences ( p > 0.05). Importantly, Bit1 expression was positively correlated with both matrix metalloproteinase 2 and Bcl-2 expression in esophageal squamous cell carcinoma and esophageal adenocarcinoma tissues ( p < 0.05). Collectively, these preliminary data support further investigation of Bit1 as an important diagnostic factor for esophageal squamous cell carcinoma and esophageal adenocarcinoma.
越来越多的证据表明,Bit1已被作为某些癌症的病因学因素进行研究,包括我们之前研究中报道的食管鳞状细胞癌,但关于Bit1在食管鳞状细胞癌和食管腺癌中可能作用的数据仍有待阐明。本研究的目的是检验Bit1是否可作为食管鳞状细胞癌和食管腺癌患者的一种新型诊断标志物。结果显示,食管鳞状细胞癌中的Bit1水平显著高于食管腺癌组织中的水平(p<0.05);值得注意的是,食管腺癌组织中的Bit1水平低于配对的正常组织,但未发现差异(p>0.05)。在食管鳞状细胞癌和食管腺癌中,Bit1的表达模式与基质金属蛋白酶2和Bcl-2完全一致。此外,不同分化程度的食管鳞状细胞癌中Bit1、Bcl-2和基质金属蛋白酶2的表达模式均高于相应的正常食管组织。低分化食管鳞状细胞癌中的Bit1表达显著高于正常食管组织(p<0.05),但在中分化和高分化食管鳞状细胞癌中则不然。低分化和中分化食管鳞状细胞癌中基质金属蛋白酶2的表达模式显著高于相应的正常食管组织(p<0.01),但在高分化食管鳞状细胞癌组织中则不然(p>0.05)。不同分化程度的食管鳞状细胞癌中Bcl-2的表达模式高于相应的正常食管组织,但无统计学差异(p>0.05)。重要的是,在食管鳞状细胞癌和食管腺癌组织中,Bit1的表达与基质金属蛋白酶2和Bcl-2的表达均呈正相关(p<0.05)。总体而言,这些初步数据支持进一步研究将Bit1作为食管鳞状细胞癌和食管腺癌的重要诊断因素。