Suppr超能文献

PAK2促进涎腺腺样囊性癌的迁移和增殖。

PAK2 promotes migration and proliferation of salivary gland adenoid cystic carcinoma.

作者信息

Deng Wei-Wei, Wu Lei, Bu Lin-Lin, Liu Jian-Feng, Li Yi-Cun, Ma Si-Rui, Yu Guang-Tao, Mao Liang, Zhang Wen-Feng, Sun Zhi-Jun

机构信息

The State Key Laboratory Breeding Base of Basic Science of Stomatology & Key Laboratory of Oral Biomedicine Ministry of Education, Wuhan University Wuhan, China.

Department of Oral and Maxillofacial-Head and Neck Oncology, School & Hospital of Stomatology, Wuhan University Wuhan 430079, China.

出版信息

Am J Transl Res. 2016 Aug 15;8(8):3387-97. eCollection 2016.

Abstract

P21 activated kinase 2 (PAK2) is a member of Group I PAKs family and highly expressed in various cancers. Current studies have demonstrated that PAK2 played a pivotal role in tumor progression. However, the role of PAK2 in salivary adenoid cystic carcinoma is still unclear. This study aims to explore the expression and the function of PAK2 in AdCC. Human salivary gland tissue microarray, including 18 normal salivary glands (NSG), 12 pleomorphic adenoma (PMA) and 72 AdCC, and immunohistochemistry were used to evaluate the expression of PAK2. The result showed that PAK2 was significantly increased in AdCC compared with NSG and PMA. Then the Pearson correlation analysis using serial tissue sections showed a close correlation of PAK2 with Cyclin D1, Phospho-STAT3 at Tyrosine 705 (p-STAT3) and Ki-67. Further in vitro study utilizing PAK2 knockdown via siRNA transfection revealed significantly reduced migration and proliferation of AdCC cell lines compared with control group. Knockdown of PAK2 decreased the expression of Cyclin D1 in AdCC cell lines. In addition, the inhibition of STAT3 reduced the expression of PAK2 in AdCC cell lines. These findings suggested that PAK2 promotes AdCC cell migration and proliferation and may be a potential therapeutic target.

摘要

p21激活激酶2(PAK2)是I组PAKs家族的成员,在多种癌症中高表达。目前的研究表明,PAK2在肿瘤进展中起关键作用。然而,PAK2在涎腺腺样囊性癌中的作用仍不清楚。本研究旨在探讨PAK2在腺样囊性癌(AdCC)中的表达及功能。采用包含18例正常涎腺(NSG)、12例多形性腺瘤(PMA)和72例AdCC的人涎腺组织芯片及免疫组化法评估PAK2的表达。结果显示,与NSG和PMA相比,AdCC中PAK2显著升高。然后,使用连续组织切片进行的Pearson相关性分析显示PAK2与细胞周期蛋白D1、酪氨酸705位点的磷酸化信号转导子和转录激活子3(p-STAT3)及Ki-67密切相关。进一步的体外研究利用小干扰RNA(siRNA)转染敲低PAK2,结果显示与对照组相比,AdCC细胞系的迁移和增殖显著降低。敲低PAK2可降低AdCC细胞系中细胞周期蛋白D1的表达。此外,抑制信号转导子和转录激活子3(STAT3)可降低AdCC细胞系中PAK2的表达。这些发现提示PAK2促进AdCC细胞迁移和增殖,可能是一个潜在的治疗靶点。

相似文献

引用本文的文献

2
Regulation of Cancer Metastasis by PAK2.PAK2对癌症转移的调控
Int J Mol Sci. 2024 Dec 15;25(24):13443. doi: 10.3390/ijms252413443.
10
P21 activated kinase 2 promotes pancreatic cancer growth and metastasis.P21激活激酶2促进胰腺癌的生长和转移。
Oncol Lett. 2019 Apr;17(4):3709-3718. doi: 10.3892/ol.2019.10040. Epub 2019 Feb 14.

本文引用的文献

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验