Suppr超能文献

伊班膦酸盐、多西他赛和法呢醇单独及联合治疗对前列腺癌细胞系生长的影响。

Differential effects of ibandronate, docetaxel and farnesol treatment alone and in combination on the growth of prostate cancer cell lines.

机构信息

Division of Urologic Oncology, Department of Urology, University of Cologne, Cologne, Germany.

出版信息

Acta Oncol. 2011 Jan;50(1):127-33. doi: 10.3109/0284186X.2010.482103. Epub 2010 Apr 29.

Abstract

Ibandronate, one of the most potent bisphosphonates, has been shown to inhibit growth of various cancer cell lines. In contrast, little is known about the effects of ibandronate on prostate cancer cells. Therefore the aim of our study was to characterize the effects of ibandronate alone and in combination with docetaxel on the growth of prostate cancer cell lines and to identify the underlying signalling pathways. Material and methods. The prostate cancer cell lines LNCaP and PC-3 were treated with increasing concentrations of ibandronate and docetaxel alone and in combination. Viable cell number was measured after five days using a hemocytometer and the MTT-method. The effects of ibandronate were tentatively antagonized by addition of farnesyl-pyrophosphate (FPP) or farnesol (FOH). Results. Ibandronate inhibits growth of both prostate cancer cell lines in a dose dependent manner. In combination with docetaxel, synergistic effects are found as evidenced by a combination index (CI) of <1. Addition of FOH and FPP completely antagonized the growth inhibitory effects of ibandronate on both cell lines. Surprisingly, in combination with ibandronate and docetaxel, FOH further increased growth inhibition instead of antagonizing the growth inhibitory effects of ibandronate. Furthermore, FOH alone appeared to be a potent inhibitor of tumor cell growth. Discussion. Ibandronate effectively inhibits growth of prostate cancer cell lines via inhibition of the farnesyl-IPP-synthase and exhibits synergistic effects with docetaxel. In addition, FOH is a potent inhibitor of prostate cancer cell lines and may display an interesting treatment option for patients with CRPC.

摘要

伊班膦酸盐是最有效的双膦酸盐之一,已被证明能抑制各种癌细胞系的生长。相比之下,关于伊班膦酸盐对前列腺癌细胞的影响知之甚少。因此,我们的研究目的是描述伊班膦酸盐单独和联合多西紫杉醇对前列腺癌细胞系生长的影响,并确定潜在的信号通路。

材料和方法。用递增浓度的伊班膦酸盐和多西紫杉醇单独和联合处理前列腺癌细胞系 LNCaP 和 PC-3。用血细胞计数器和 MTT 法在 5 天后测量活细胞数。通过添加法呢基焦磷酸(FPP)或法呢醇(FOH),暂时拮抗伊班膦酸盐的作用。

结果。伊班膦酸盐以剂量依赖的方式抑制两种前列腺癌细胞系的生长。与多西紫杉醇联合使用时,发现协同作用,组合指数(CI)<1。添加 FOH 和 FPP 完全拮抗伊班膦酸盐对两种细胞系的生长抑制作用。令人惊讶的是,与伊班膦酸盐和多西紫杉醇联合使用时,FOH 进一步增加了肿瘤细胞生长的抑制作用,而不是拮抗伊班膦酸盐的生长抑制作用。此外,FOH 本身似乎是一种有效的肿瘤细胞生长抑制剂。

讨论。伊班膦酸盐通过抑制法尼基异戊烯基焦磷酸合酶有效抑制前列腺癌细胞系的生长,并与多西紫杉醇表现出协同作用。此外,FOH 是前列腺癌细胞系的有效抑制剂,可能为 CRPC 患者提供一种有趣的治疗选择。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验