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选择性环氧化酶2抑制剂塞来昔布对人前列腺癌细胞系PC-3增殖和凋亡的影响

[Effects of a selective cyclooxygenase 2 inhibitor celecoxib on the proliferation and apoptosis of human prostate cancer cell line PC-3].

作者信息

Xu Song, Zhou Wen-quan, Zhang Zheng-yu, Ge Jing-ping, Gao Jian-ping

机构信息

Department of Urology, Nanjing School of Clinical Medicine, the Second Military Medical University/Nanjing General Hospital of Nanjing Military Command, PLA, Nanjing, Jiangsu 210002, China.

出版信息

Zhonghua Nan Ke Xue. 2008 Jun;14(6):489-93.

Abstract

OBJECTIVE

To investigate the anti-tumor effect of celecoxib on human prostate cancer cell line PC-3 in vitroby observing its effects on the proliferation and apoptosis of PC-3 cells.

METHODS

The effects of Celecoxib on the proliferation of PC-3 cells were observed by MTT assay, erosion trace test and Transwell-chamber chemotaxis assay, and their apoptosis detected by Annexin V/FITC fluorescent staining and flow cytometry.

RESULTS

With the increasing concentration and exposure time, Celecoxib exhibited an increased rate of inhibition on PC-3 cells in a dose- and time-dependent manner (P < 0.05). Compared with the controls, the migration distance of the PC-3 cells and the number of the PC-3 cells that invaded the inferior chamber were significantly decreased in the 100 gm/L Celecoxib group (P < 0.05). Celecoxib induced the apoptosis of PC-3 cells and, at 100 microm/L, significantly increased the percentage of PC-3 cells in the G0/G1 phase but decreased it in the S phase as compared with the control group (P < 0.05).

CONCLUSION

Celecoxib inhibits the proliferation and induces the apoptosis of PC-3 cells in vitro, which, as a new therapeutic for prostate cancer, well deserves further investigation.

摘要

目的

通过观察塞来昔布对人前列腺癌细胞系PC-3增殖和凋亡的影响,探讨其体外抗肿瘤作用。

方法

采用MTT法、划痕试验和Transwell小室趋化试验观察塞来昔布对PC-3细胞增殖的影响,采用Annexin V/FITC荧光染色和流式细胞术检测其凋亡情况。

结果

随着浓度增加和作用时间延长,塞来昔布对PC-3细胞的抑制率呈剂量和时间依赖性增加(P<0.05)。与对照组相比,100μg/L塞来昔布组PC-3细胞迁移距离及侵袭至下室的细胞数明显减少(P<0.05)。塞来昔布诱导PC-3细胞凋亡,100μmol/L时与对照组相比,PC-3细胞G0/G1期百分比明显增加,S期百分比降低(P<0.05)。

结论

塞来昔布体外抑制PC-3细胞增殖并诱导其凋亡,作为前列腺癌的一种新的治疗方法,值得进一步研究。

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