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干扰素-β对塞来昔布在U87胶质瘤模型中抗肿瘤活性的抑制作用。

Inhibitory Effect of IFN-beta, on the Antitumor Activity of Celecoxib in U87 Glioma Model.

作者信息

Kim Eun-Kyoung, Chung Dong-Sup, Shin Hye-Jin, Hong Yong-Kil

机构信息

The Catholic University of Korea College of Medicine, Kangnam St. Mary's Hospital, Seoul, Korea.

出版信息

J Korean Neurosurg Soc. 2009 Dec;46(6):552-7. doi: 10.3340/jkns.2009.46.6.552. Epub 2009 Dec 31.

Abstract

OBJECTIVE

Interferon-beta, (IFN-beta) has been used in the treatment of cancers. Inhibition of the enzyme cyclooxygenase (COX) with celecoxib had a significantly suppressive effect on tumor growth, angiogenesis, and metastasis in a variety of tumors. The aim of this study was to elucidate the antiglioma effect of combined treatment with IFN-beta and celecoxib in U87 glioma model.

METHODS

The in vitro effects of IFN-beta (50-1,000 IU/mL) and celecoxib (50-250 microM) alone or combination of both on the proliferation and apoptosis of U87 cells were tested using MTT assay, FACS analysis and DNA condensation. To determine the in vivo effect, nude mice bearing intracerebral U87 xenograft inoculation were treated with IFN-beta intraperitoneally (2x10(5) IU/day for 15 days), celecoxib orally (5, 10 mg/kg) or their combination.

RESULTS

IFN-beta or celecoxib showed an inhibitory effect on the proliferation of U87 cells. When U87 cells were treated with IFN-beta and celecoxib combination, it seemed that IFN-beta interrupted the antiproliferative and apoptotic activity of celecoxib. No additive effect was observed on the survival of the tumor bearing mice by the combination of IFN-beta and celecoxib.

CONCLUSION

These results suggest that IFN-beta seems to inhibit the antiglioma effect of celecoxib, therefore combination of IFN-beta and celecoxib may be undesirable in the treatment of glioma.

摘要

目的

β-干扰素(IFN-β)已用于癌症治疗。塞来昔布抑制环氧化酶(COX)对多种肿瘤的肿瘤生长、血管生成和转移具有显著的抑制作用。本研究的目的是阐明IFN-β与塞来昔布联合治疗在U87胶质瘤模型中的抗胶质瘤作用。

方法

使用MTT法、流式细胞术分析和DNA凝聚检测单独使用IFN-β(50 - 1000 IU/mL)和塞来昔布(50 - 250 μM)或两者联合对U87细胞增殖和凋亡的体外影响。为确定体内作用,对脑内接种U87异种移植物的裸鼠进行腹腔注射IFN-β(2×10⁵ IU/天,共15天)、口服塞来昔布(5、10 mg/kg)或两者联合治疗。

结果

IFN-β或塞来昔布对U87细胞的增殖均有抑制作用。当U87细胞用IFN-β和塞来昔布联合处理时,IFN-β似乎中断了塞来昔布的抗增殖和凋亡活性。IFN-β和塞来昔布联合对荷瘤小鼠的存活未观察到相加作用。

结论

这些结果表明IFN-β似乎抑制了塞来昔布的抗胶质瘤作用,因此IFN-β与塞来昔布联合可能不适用于胶质瘤治疗。

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