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环氧化酶-2抑制剂塞来昔布通过降低基质金属蛋白酶-2和-9的活性来抑制鼻咽癌细胞系的侵袭和迁移。

Cyclooxygenase-2 inhibitor celecoxib suppresses invasion and migration of nasopharyngeal carcinoma cell lines through a decrease in matrix metalloproteinase-2 and -9 activity.

作者信息

Li Wen-Wen, Long Guo-Xian, Liu Dong-Bo, Mei Qi, Wang Jun-Feng, Hu Guang-Yuan, Jiang Ji-Zong, Sun Wei, Gan Lei, Hu Guo-Qing

出版信息

Pharmazie. 2014 Feb;69(2):132-7.

Abstract

Celecoxib is a selective inhibitor of COX-2, whose connection with the development and progression of human tumors has been extensively studied. So far, however, its anti-metastatic effect is poorly understood in nasopharyngeal carcinoma. The current study aimed to observe the effect of celecoxib on invasion and migration of nasopharyngeal carcinoma cell lines and investigate the potential mechanism in vitro. Human nasopharyngeal carcinoma cell lines HNE1, HONE1, SUNE1-5-8F were exposed to different concentrations of celecoxib. MTT assay was used to study its anti-proliferation effect, transwell assay wound healing repair assay were performed to investigate the invasiveness and migration capability after treatment with celecoxib. The activity of MMP-2 and MMP-9 was measured by gelatin zymography. MTT assay showed that celecoxib inhibited HNE1, HONE1, and SUNE1-5-8F cells growth. Wound healing repair assay and transwell assay showed that cell metastatic ability was suppressed after treatment with celecoxib. Celecoxib had a significant inhibitory effect on the activity of MMP-2/9 in a dose-dependent manner in HNE1, HONE1 and SUNE1-5-8F cell lines. These data demonstrated that celecoxib-induced suppression of MMP-2 and MMP-9 activity might be involved in the inhibition of nasopharyngeal carcinoma cell lines invasion and migration.

摘要

塞来昔布是一种环氧化酶-2(COX-2)的选择性抑制剂,其与人类肿瘤发生发展的关系已得到广泛研究。然而,目前其在鼻咽癌中的抗转移作用尚不清楚。本研究旨在观察塞来昔布对鼻咽癌细胞系侵袭和迁移的影响,并在体外探讨其潜在机制。将人鼻咽癌细胞系HNE1、HONE1、SUNE1-5-8F暴露于不同浓度的塞来昔布中。采用MTT法研究其抗增殖作用,进行Transwell实验和伤口愈合修复实验以研究塞来昔布处理后细胞的侵袭和迁移能力。通过明胶酶谱法检测基质金属蛋白酶-2(MMP-2)和基质金属蛋白酶-9(MMP-9)的活性。MTT实验表明,塞来昔布抑制HNE1、HONE1和SUNE1-5-8F细胞的生长。伤口愈合修复实验和Transwell实验表明,塞来昔布处理后细胞的转移能力受到抑制。塞来昔布对HNE1、HONE1和SUNE1-5-8F细胞系中MMP-2/9的活性具有显著的剂量依赖性抑制作用。这些数据表明,塞来昔布诱导的MMP-2和MMP-9活性抑制可能参与了对鼻咽癌细胞系侵袭和迁移的抑制。

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