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舒林酸在口腔癌中不依赖环氧化酶的抗肿瘤作用是通过下调生存素介导的。

COX-independent antineoplastic effects of sulindac in oral cancer are mediated by survivin down-regulation.

作者信息

Scheper Mark A, Sauk John J, Nikitakis Nikolaos G

机构信息

Department of Diagnostic Sciences and Pathology, Dental School, University of Maryland, Baltimore, MD 21201, USA.

出版信息

Anticancer Res. 2006 Nov-Dec;26(6B):4103-13.

Abstract

BACKGROUND

Cyclooxygenase (COX) inhibitors are reported to exert anti-proliferative and pro-apoptotic effects on cancer. The effects of COX inhibitors on oral squamous cell carcinoma (SCC) and survivin expression were assessed.

MATERIALS AND METHODS

Primary oral SCC were analyzed immunohistochemically, and oral SCC cell lines were assessed using RT-PCR, Western blot, cell proliferation and apoptosis assays, following treatment with various COX inhibitors, SiRNA against survivin, or survivin forced expression.

RESULTS

Survivin was expressed in all studied tumors. SiRNA against survivin or treatment with sulindac, but not other COX inhibitors, decreased survivin expression and tumor cell proliferation and increased apoptosis. Forced expression of survivin attenuated sulindac's effects.

CONCLUSION

Survivin is implicated as a marker and treatment target in oral SCC, inhibition of which causes reduction of cell proliferation and induction of apoptosis. Down-regulation of survivin expression by sulindac provides an explanation for its antineoplastic effects.

摘要

背景

据报道,环氧化酶(COX)抑制剂对癌症具有抗增殖和促凋亡作用。评估了COX抑制剂对口腔鳞状细胞癌(SCC)和生存素表达的影响。

材料与方法

对原发性口腔SCC进行免疫组织化学分析,并用各种COX抑制剂、针对生存素的小干扰RNA(SiRNA)或生存素强制表达处理后,使用逆转录-聚合酶链反应(RT-PCR)、蛋白质免疫印迹法、细胞增殖和凋亡检测法对口腔SCC细胞系进行评估。

结果

在所研究的所有肿瘤中均有生存素表达。针对生存素的SiRNA或舒林酸处理可降低生存素表达并减少肿瘤细胞增殖,增加细胞凋亡,但其他COX抑制剂无此作用。生存素的强制表达减弱了舒林酸的作用。

结论

生存素被认为是口腔SCC的一个标志物和治疗靶点,抑制生存素可导致细胞增殖减少和凋亡诱导。舒林酸使生存素表达下调,这为其抗肿瘤作用提供了解释。

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