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Fra-1 调节 HMGA1 的表达,HMGA1 与人类食管鳞状细胞癌的不良预后相关。

Fra-1 Regulates the Expression of HMGA1, Which is Associated with a Poor Prognosis in Human Esophageal Squamous Cell Carcinoma.

机构信息

Department of Frontier Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.

出版信息

Ann Surg Oncol. 2017 Oct;24(11):3446-3455. doi: 10.1245/s10434-016-5666-5. Epub 2016 Nov 23.

Abstract

BACKGROUND

The expression of Fos-related antigen 1 (Fra-1) affects tumor progression, migration, and invasion. In this study, we identified the genes regulated by Fra-1 in esophageal squamous cell carcinoma (ESCC).

METHODS

We constructed Fra-1 knockdown models via the transfection of small interfering RNA (siRNA) into ESCC cell lines (TE10, TE11). The expression levels of the genes in the knockdown models were analyzed using a microarray and a Biobase Upstream Analysis, while the expression levels of the candidate genes in the primary tumors of surgical specimens obtained from ESCC patients were determined using real-time polymerase chain reaction (PCR) and immunohistochemical staining. The clinicopathological features were then analyzed.

RESULTS

The Biobase Upstream Analysis showed the high-mobility-group protein-1 (HMGA1) to be a significant gene regulated by Fra-1. Actual binding of Fra-1 to the promotor region of HMGA1 was revealed in subsequent chromatin immunoprecipitation PCR experiments. Patients with a positive HMGA1 expression had a poor prognosis, and a multivariate analysis demonstrated a positive HMGA1 expression to be a significant independent prognostic factor.

CONCLUSION

HMGA1 is regulated by Fra-1 in ESCC, and the HMGA1 expression is significantly associated with a poor prognosis in ESCC patients. Downregulation of the HMGA1 expression may become a practical treatment strategy against ESCC in the future.

摘要

背景

Fos 相关抗原 1(Fra-1)的表达影响肿瘤的进展、迁移和侵袭。在本研究中,我们鉴定了 Fra-1 在食管鳞状细胞癌(ESCC)中调控的基因。

方法

我们通过转染小干扰 RNA(siRNA)构建 Fra-1 敲低模型,用于 ESCC 细胞系(TE10、TE11)。使用微阵列和 Biobase Upstream Analysis 分析敲低模型中基因的表达水平,同时使用实时聚合酶链反应(PCR)和免疫组织化学染色检测 ESCC 患者手术标本中候选基因的表达水平。然后分析临床病理特征。

结果

Biobase Upstream Analysis 显示高迁移率族蛋白 1(HMGA1)是 Fra-1 调控的显著基因。随后的染色质免疫沉淀 PCR 实验显示 Fra-1 与 HMGA1 启动子区域的实际结合。HMGA1 表达阳性的患者预后较差,多变量分析表明 HMGA1 表达阳性是 ESCC 患者的一个显著独立预后因素。

结论

HMGA1 在 ESCC 中受 Fra-1 调控,HMGA1 的表达与 ESCC 患者的不良预后显著相关。下调 HMGA1 的表达可能成为未来 ESCC 治疗的一种实用策略。

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