Zhang Jian, Zhi Huiying, Zhou Chuannong, Ding Fang, Luo Aiping, Zhang Xun, Sun Yuntian, Wang Xiuqin, Wu Min, Liu Zhihua
National Laboratory of Molecular Oncology, Cancer Institute and Hospital, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing, People's Republic of China.
J Pathol. 2005 Dec;207(4):402-9. doi: 10.1002/path.1846.
Fibronectin (FN) was found to be up-regulated in human oesophageal squamous cell carcinoma (ESCC) by cDNA microarray analysis in our laboratory. In order to elucidate the chronology of FN expression at various stages of oesophageal carcinogenesis, RT-PCR, immunohistochemistry and Western blot analysis were carried out on ESCC tissue samples with different pathological characteristics. FN was mainly localized in the interstitial tissues, and its up-regulation in ESCC was significantly associated with the depth of invasion by carcinoma (R = 0.803, p < 0.01). To investigate its relationship with the Erk pathway further, pRaf-1 and pErk-1/2 expression were also analysed in ESCC. Activation of Erk1/2 and Raf was identified in 63.3% and 60.3% of the tumour specimens, respectively, whereas normal mucosal epithelial tissues were negative. Moreover, a close association was observed between pErk-1/2 expression and the differentiation grade (R = -0.421, p = 0.002): pErk-1/2 signal was greater in poorly differentiated tissues than in well and moderately differentiated tissues. Co-expression of FN and pErk-1/2 was found at the invasive front of tumour nests by double immunofluorescence staining and there was a statistical correlation between the expression of FN and pErk-1/2 (p < 0.05). In the cell line EC9706, plasma FN was able to phosphorylate Raf and further activate Erk, but it did not alter MMP-2 protein expression or activity, indicating that MMP-2 may not be the downstream target gene of the Erk pathway. All the above data suggest that the up-regulation of FN contributes to the later stage of oesophageal carcinogenesis, and that activation of the Erk pathway may be involved in the roles of FN in ESCC.
在我们实验室通过cDNA微阵列分析发现,纤连蛋白(FN)在人食管鳞状细胞癌(ESCC)中上调。为了阐明食管癌变各个阶段FN表达的时间顺序,对具有不同病理特征的ESCC组织样本进行了逆转录聚合酶链反应(RT-PCR)、免疫组织化学和蛋白质印迹分析。FN主要定位于间质组织,其在ESCC中的上调与癌组织的浸润深度显著相关(R = 0.803,p < 0.01)。为了进一步研究其与细胞外信号调节激酶(Erk)通路的关系,还对ESCC中的磷酸化Raf-1和磷酸化Erk-1/2表达进行了分析。分别在63.3%和60.3%的肿瘤标本中检测到Erk1/2和Raf的激活,而正常黏膜上皮组织为阴性。此外,观察到磷酸化Erk-1/2表达与分化程度密切相关(R = -0.421,p = 0.002):低分化组织中的磷酸化Erk-1/2信号高于高分化和中分化组织。通过双重免疫荧光染色在肿瘤巢的浸润前沿发现了FN和磷酸化Erk-1/2的共表达,并且FN和磷酸化Erk-1/2的表达之间存在统计学相关性(p < 0.05)。在细胞系EC9706中,血浆FN能够使Raf磷酸化并进一步激活Erk,但它没有改变基质金属蛋白酶-2(MMP-2)的蛋白表达或活性,表明MMP-2可能不是Erk通路的下游靶基因。上述所有数据表明,FN的上调有助于食管癌变的后期发展,并且Erk通路的激活可能参与了FN在ESCC中的作用。