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甲状腺乳头状癌中AP-2α的表达预示肿瘤进展及预后不良。

AP-2α expression in papillary thyroid carcinoma predicts tumor progression and poor prognosis.

作者信息

Wu Hong Rong, Zhang Jian

机构信息

Department of Pathology, The Xiangya Hospital of Central South University, Changsha, Hunan, 410008, China,

出版信息

Cancer Manag Res. 2018 Aug 13;10:2615-2625. doi: 10.2147/CMAR.S167874. eCollection 2018.

Abstract

BACKGROUND

The activator protein (AP)-2α is involved in a wide variety of biologic processes in tumor. However, little is known about the role of AP-2α in human papillary thyroid carcinoma (PTC).

METHODS

The immunohistochemical method was used to detect AP-2α expression in 63 PTC cases. Western blotting was carried out to assess the change in expression of certain proteins. The bioinformatics analysis of 496 PTC samples comes from The Cancer Genome Atlas (TCGA). The Gene Set Enrichment Analysis (GSEA) was performed using TCGA data set. Cell transfection was used to induce related protein expression or to repress it by RNA interference procedures.

RESULTS

Our results demonstrated that AP-2α expression was higher in tumor tissues than the corresponding adjacent nontumor tissues, the positive substances of AP-2α were observed mainly in the cytoplasm of PTC, and AP-2α was positively correlated with histologic type (=0.026) of PTC patients. The high expression of AP-2α mRNA was associated significantly with tumor stages (=0.011), histologic type (=0.019), and independently predicted shorter overall survival (=0.005) based on TCGA analysis. Patients with high AP-2α mRNA expression have shorter overall survival compared to those with low AP-2α mRNA expression, particularly in advanced tumor stages (III and IV) of PTC patients (=0.011). Multivariate analysis suggested that AP-2α mRNA expression might be an independent prognostic indicator for the survival of patients with PTC (=0.037). Moreover, the association between enhanced AP-2α expression and two pathways (notch signaling and focal adhesion) was revealed by GSEA, and then confirmed by cellular experiments.

CONCLUSION

Taken together, our findings suggest that AP-2α may be a potential prognostic molecular marker and therapeutic target for PTC patients.

摘要

背景

激活蛋白(AP)-2α参与肿瘤中的多种生物学过程。然而,关于AP-2α在人甲状腺乳头状癌(PTC)中的作用知之甚少。

方法

采用免疫组织化学方法检测63例PTC病例中AP-2α的表达。进行蛋白质印迹法以评估某些蛋白质表达的变化。对来自癌症基因组图谱(TCGA)的496例PTC样本进行生物信息学分析。使用TCGA数据集进行基因集富集分析(GSEA)。通过细胞转染诱导相关蛋白表达或通过RNA干扰程序抑制其表达。

结果

我们的结果表明,肿瘤组织中AP-2α的表达高于相应的相邻非肿瘤组织,AP-2α的阳性物质主要在PTC的细胞质中观察到,并且AP-2α与PTC患者的组织学类型呈正相关(=0.026)。基于TCGA分析,AP-2α mRNA的高表达与肿瘤分期(=0.011)、组织学类型(=0.019)显著相关,并且独立预测总体生存期较短(=0.005)。与AP-2α mRNA低表达的患者相比,AP-2α mRNA高表达的患者总体生存期较短,特别是在PTC患者的晚期肿瘤阶段(III和IV期)(=0.011)。多变量分析表明,AP-2α mRNA表达可能是PTC患者生存的独立预后指标(=0.037)。此外,GSEA揭示了增强的AP-2α表达与两条途径(Notch信号通路和粘着斑)之间的关联,随后通过细胞实验得到证实。

结论

综上所述,我们的研究结果表明,AP-2α可能是PTC患者潜在的预后分子标志物和治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a39/6095110/c6b5280f9d9b/cmar-10-2615Fig1.jpg

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