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RAD001(依维莫司)可抑制前列腺癌在骨骼中的生长,与多西他赛和唑来膦酸联合使用时,其抑制作用会增强。

RAD001 (Everolimus) inhibits growth of prostate cancer in the bone and the inhibitory effects are increased by combination with docetaxel and zoledronic acid.

作者信息

Morgan Todd M, Pitts Tiffany E M, Gross Ted S, Poliachik Sandra L, Vessella Robert L, Corey Eva

机构信息

Department of Urology, University of Washington School of Medicine, Seattle, Washington 98195, USA.

出版信息

Prostate. 2008 Jun 1;68(8):861-71. doi: 10.1002/pros.20752.

Abstract

INTRODUCTION

mTOR activity is increased in advanced prostate cancer (CaP) as a result of a high rate of PTEN mutations. RAD001 (Everolimus) is a new orally available mTOR inhibitor. The objective of our study was to evaluate the effects of RAD001 on the growth of CaP in the bone, both alone and in combination with docetaxel and zoledronic acid.

METHODS

C4-2 CaP cells were injected into tibiae of mice and the animals were treated with RAD001, docetaxel, and zoledronic acid alone or in combination. Histomorphometrical analysis, serum PSA measurements, bone mineral density (BMD), and microCT were used to determine the effects of treatment on tumor and bone.

RESULTS

All three agents alone decreased tumor volume, and RAD001 and docetaxel also decreased levels of serum PSA by 68% and 65%, respectively (both P < 0.01). Combinations of the agents were more effective in decreasing tumor volume than single agents. Three-drug treatment showed the greatest effect: 64% inhibition versus control (P < 0.01). Treatment with RAD001 interfered with the weight loss associated with growth of this tumor in the bone (non-RAD001 groups: 4.0% decrease in body weight, P = 0.0014; RAD001 groups: increase of 3.6% in body weight, P = 0.0037).

CONCLUSIONS

RAD001 inhibited growth of C4-2 cells in bone, an effect augmented by addition of docetaxel and zoledronic acid. Moreover RAD001 had a significant impact on maintenance of body weight. RAD001 may hold promise for its effects on both metastatic CaP and the important syndrome of tumor cachexia.

摘要

引言

由于PTEN突变率高,晚期前列腺癌(CaP)中mTOR活性增加。RAD001(依维莫司)是一种新型口服mTOR抑制剂。我们研究的目的是评估RAD001单独以及与多西他赛和唑来膦酸联合使用对骨中CaP生长的影响。

方法

将C4-2 CaP细胞注射到小鼠胫骨中,然后将动物单独或联合使用RAD001、多西他赛和唑来膦酸进行治疗。采用组织形态计量分析、血清PSA测量、骨矿物质密度(BMD)和微型CT来确定治疗对肿瘤和骨骼的影响。

结果

所有三种药物单独使用均能减小肿瘤体积,RAD001和多西他赛还分别使血清PSA水平降低了68%和65%(均P<0.01)。联合用药在减小肿瘤体积方面比单一药物更有效。三联药物治疗效果最佳:与对照组相比抑制率为64%(P<0.01)。RAD001治疗可抑制该骨肿瘤生长相关的体重减轻(非RAD001组:体重下降4.0%,P = 0.0014;RAD001组:体重增加3.6%,P = 0.0037)。

结论

RAD001抑制骨中C4-2细胞的生长,多西他赛和唑来膦酸的加入可增强这一作用。此外,RAD001对维持体重有显著影响。RAD001可能因其对转移性CaP和重要的肿瘤恶病质综合征的作用而具有前景。

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本文引用的文献

1
The role of mammalian target of rapamycin inhibitors in the treatment of advanced renal cancer.
Clin Cancer Res. 2007 Jan 15;13(2 Pt 2):758s-763s. doi: 10.1158/1078-0432.CCR-06-1986.
2
Combining an mTOR antagonist and receptor tyrosine kinase inhibitors for the treatment of prostate cancer.
Cancer Biol Ther. 2007 Feb;6(2):195-201. doi: 10.4161/cbt.6.2.3588. Epub 2007 Feb 7.
3
Hypothalamic mTOR signaling regulates food intake.
Science. 2006 May 12;312(5775):927-30. doi: 10.1126/science.1124147.
4
Effect of zoledronic acid on pain associated with bone metastasis in patients with prostate cancer.
Ann Oncol. 2006 Jun;17(6):986-9. doi: 10.1093/annonc/mdl041. Epub 2006 Mar 13.
6
Weekly docetaxel and zoledronic acid every 4 weeks in hormone-refractory prostate cancer patients.
Cancer Chemother Pharmacol. 2006 Jan;57(1):46-51. doi: 10.1007/s00280-005-0025-4. Epub 2005 Nov 5.
10
Osteoprotegerin in prostate cancer bone metastasis.
Cancer Res. 2005 Mar 1;65(5):1710-8. doi: 10.1158/0008-5472.CAN-04-2033.

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