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多聚(C)结合蛋白1(PCBP1)在非小细胞肺癌中作为上皮-间质转化的负调节因子的表达及其临床价值。

Expression of poly(C)-binding protein 1 (PCBP1) in NSCLC as a negative regulator of EMT and its clinical value.

作者信息

Liu Yifei, Gai Ling, Liu Jian, Cui Yuan, Zhang Yan, Feng Jia

机构信息

Department of Pathology, Affiliated Hospital of Nantong University Nantong 226001, Jiangsu, China.

Department of Oncology, Affiliated Hospital of Nantong University Nantong 226001, Jiangsu, China.

出版信息

Int J Clin Exp Pathol. 2015 Jun 1;8(6):7165-72. eCollection 2015.

Abstract

Poly (C)-binding Protein 1 (PCBP1) is a 35 kDa protein involved in a number of biological processes. Recently, the research found that PCBP1 might be involved in epithelial-mesenchymal transition (EMT). However, the role of PCBP1 in non-small-cell lung cancer (NSCLC) metastasis needs further elucidation. The purpose of this study was to determine whether PCBP1 could serve as a biomarker for stratification and prediction of prognosis in NSCLC as a regulator of EMT formation. In this study, PCBP1 expression was evaluated by Western blot in 8 fresh lung cancer tissues and immunohistochemistry (IHC) on 145 paraffin-embedded slices. PCBP1 was highly expressed in non-metastatic NSCLC specimens and significantly correlated with lymph node status (P < 0.001), clinical stage (P = 0.001), vimentin expression (P = 0.033) and E-cadherin expression (P = 0.042). Our study showed that the low expression of PCBP1 was correlated with decreased expression of E-cadherin and elevated expression of vimentin, which were the markers of EMT. Besides, high expression of PCBP1 was correlated with better prognosis. These findings suggested that PCBP1 might play an important role in preventing the process of EMT in NSCLC, thus be a promising therapeutic target to inhibit NSCLC metastasis.

摘要

多聚(C)结合蛋白1(PCBP1)是一种参与多种生物学过程的35 kDa蛋白。最近,研究发现PCBP1可能参与上皮-间质转化(EMT)。然而,PCBP1在非小细胞肺癌(NSCLC)转移中的作用仍需进一步阐明。本研究的目的是确定PCBP1作为EMT形成的调节因子,是否可作为NSCLC分层和预后预测的生物标志物。在本研究中,通过蛋白质免疫印迹法评估了8例新鲜肺癌组织中PCBP1的表达,并对145张石蜡包埋切片进行了免疫组织化学(IHC)检测。PCBP1在非转移性NSCLC标本中高表达,且与淋巴结状态(P < 0.001)、临床分期(P = 0.001)、波形蛋白表达(P = 0.033)和E-钙黏蛋白表达(P = 0.042)显著相关。我们的研究表明,PCBP1低表达与EMT标志物E-钙黏蛋白表达降低和波形蛋白表达升高相关。此外,PCBP1高表达与较好的预后相关。这些发现提示PCBP1可能在阻止NSCLC的EMT进程中发挥重要作用,因此有望成为抑制NSCLC转移的治疗靶点。

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