Luo Fan-Yan, Liu Zi-Hou, Hu Qin-Hua, Lin Guo-Qiang, Tang Can-E, Zhang Wei-Xing, Zhuang Wei
1. Department of Cardiothoracic Surgery, Xiangya Hospital, Central South University;
2. Institute of Medical Sciences, Xiangya Hospital, Central South University, Changsha 410008, China.
J Cancer. 2015 Mar 26;6(5):477-81. doi: 10.7150/jca.11715. eCollection 2015.
Metastasis in lung cancer portends a poor prognosis, and the epithelial-mesenchymal transition (EMT) in lung cancer cells is considered a prerequisite to achieve metastatic potential. Recent studies indicate that BTB/POZ domain-containing protein 7 (BTBD7) regulates EMT-associated proteins in human malignancies and however, the role of BTBD7 in lung cancer have not been identified. In present study, we examined BTBD7 expression status and its association with unfavorable clinical features in non-small-cell lung cancer (NSCLC). Firstly, we studied the fresh specimens, and found that both mRNA and protein expression levels of BTBD7 in NSCLC tissue were significantly increased compared with the adjacent nontumorous lung tissue. Then, we determined BTBD7 protein expressions in the paraffin-embedded samples from NSCLC patients, and analyzed the relations of BTBD7 expression with clinicopathologic features of the patients. The results showed that incidence of metastasis in patients with positive BTBD7 expression was significantly higher than that in those with negative BTBD7 expression, and the positive BTBD7 expression rate in metastatic cases was significantly higher than that in non-metastatic ones; furthermore, Cox regression analyses revealed that BTBD7 was an independent risk factor for either metastasis or survival in NSCLC patients. Thus, we conclude that BTBD7 contributes to metastasis of NSCLC and BTBD7-positive NSCLC may have a high potential for metastasis and thereby a poor prognosis.
肺癌转移预示着预后不良,肺癌细胞中的上皮-间质转化(EMT)被认为是获得转移潜能的先决条件。最近的研究表明,含BTB/POZ结构域蛋白7(BTBD7)在人类恶性肿瘤中调节与EMT相关的蛋白,然而,BTBD7在肺癌中的作用尚未明确。在本研究中,我们检测了非小细胞肺癌(NSCLC)中BTBD7的表达状态及其与不良临床特征的关系。首先,我们研究了新鲜标本,发现NSCLC组织中BTBD7的mRNA和蛋白表达水平均显著高于相邻的非肿瘤肺组织。然后,我们测定了NSCLC患者石蜡包埋样本中BTBD7蛋白的表达,并分析了BTBD7表达与患者临床病理特征的关系。结果显示,BTBD7表达阳性患者的转移发生率显著高于BTBD7表达阴性患者,转移病例中BTBD7阳性表达率显著高于非转移病例;此外,Cox回归分析显示,BTBD7是NSCLC患者转移或生存的独立危险因素。因此,我们得出结论,BTBD7促进NSCLC转移,BTBD7阳性的NSCLC可能具有较高的转移潜能,从而预后不良。