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富含酸性亮氨酸的核磷蛋白32A(ANP32A)与淋巴结转移相关,提示口腔鳞状细胞癌患者预后不良。

Acidic leucine-rich nuclear phosphoprotein-32A (ANP32A) association with lymph node metastasis predicts poor survival in oral squamous cell carcinoma patients.

作者信息

Velmurugan Bharath Kumar, Yeh Kun-Tu, Lee Chien-Hung, Lin Shu-Hui, Chin Mei-Chung, Chiang Shang-Lun, Wang Zhi-Hong, Hua Chun-Hung, Tsai Ming-Hsui, Chang Jan-Gowth, Ko Ying-Chin

机构信息

Environment-Omics-Diseases Research, China Medical University Hospital, Taichung, Taiwan.

Department of Pathology, Changhua Christian Hospital, Changhua, Taiwan.

出版信息

Oncotarget. 2016 Mar 8;7(10):10879-90. doi: 10.18632/oncotarget.7681.

Abstract

Acidic leucine-rich nuclear phosphoprotein-32A (ANP32A) is a multifunctional protein aberrantly expressed in various types of cancers. However, its expression pattern and clinical significance in oral squamous cell carcinoma (OSCC) remains unclear. In this study, we immunohistochemically investigated the expression pattern of ANP32A in 259 OSCC patients and the results were correlated with clinicopathological factors using Allred, Klein and Immunoreactive scoring (IRS) system. Our data indicated that high expression of ANP32A was significantly associated with N stage and tumor differentiation status in OSCC patients. High ANP32A expression with N2/N3 stage had an increased mortality risk than low ANP32A expressing OSCC patients with N0/N1 stage. Functional studies revealed that knockdown of ANP32A significantly decreased the migration and invasion ability thereby concomitantly increasing E-cadherin and decreasing Slug, Claudin-1 and Vimentin expression in vitro. These results suggest that ANP32A is commonly increased in oral squamous cell carcinoma and ANP32A protein could act as a potential biomarker for prognosis assessment of oral cancer patients with lymph node metastasis.

摘要

富含酸性亮氨酸的核磷蛋白32A(ANP32A)是一种在多种癌症中异常表达的多功能蛋白。然而,其在口腔鳞状细胞癌(OSCC)中的表达模式和临床意义仍不清楚。在本研究中,我们采用免疫组织化学方法研究了259例OSCC患者中ANP32A的表达模式,并使用奥尔雷德、克莱因和免疫反应评分(IRS)系统将结果与临床病理因素相关联。我们的数据表明,ANP32A的高表达与OSCC患者的N分期和肿瘤分化状态显著相关。与N0/N1期低表达ANP32A的OSCC患者相比,N2/N3期高表达ANP32A的患者死亡风险增加。功能研究表明,在体外敲低ANP32A可显著降低迁移和侵袭能力,从而同时增加E-钙黏蛋白的表达,并降低Slug、Claudin-1和波形蛋白的表达。这些结果表明,ANP32A在口腔鳞状细胞癌中普遍升高,ANP32A蛋白可作为评估有淋巴结转移口腔癌患者预后的潜在生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c57/4905446/83ae4e71cda6/oncotarget-07-10879-g001.jpg

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