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二甲双胍与丙戊酸联合使用对前列腺癌生长的抗肿瘤作用比单独使用任何一种药物都更强。

The Combination of Metformin and Valproic Acid Has a Greater Anti-tumoral Effect on Prostate Cancer Growth than Either Drug Alone.

作者信息

Tran Linh N K, Kichenadasse Ganessan, Morel Katherine L, Lavranos Tina C, Klebe Sonja, Lower Karen M, Ormsby Rebecca J, Elliot David J, Sykes Pamela J

机构信息

Flinders Centre for Innovation in Cancer, Flinders University and Medical Centre, Adelaide, South Australia

University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh, Vietnam.

出版信息

In Vivo. 2019 Jan-Feb;33(1):99-108. doi: 10.21873/invivo.11445.

Abstract

BACKGROUND/AIM: The hypoglycemic drug metformin (MET) and the anti-epileptic drug valproic acid (VPA) have individually shown anti-tumor effects in prostate cancer in vitro. The present study intended to investigate the efficacy of the combination of MET and VPA in prostate cancer treatment in a pre-clinical xenograft model.

MATERIALS AND METHODS

Prostate cancer cell lines (LNCaP and PC-3) were inoculated under the skin of BALB/c nude mice. The mice were treated with 200 μl/ml MET and/or 0.4% (w/v) VPA diluted in drinking water, or with vehicle control, and were monitored until the tumor volume reached 2,000 mm Evaluation of toxicity of the drug combination was determined in liver and kidney by histology.

RESULTS

In both LNCaP and PC-3 xenografts, MET combined with VPA significantly reduced tumor growth during the first 4 weeks following treatment, and delayed the time-to-tumor volume of 2,000 mm by 90 days, as compared to MET or to VPA alone, and to vehicle control. There was no significant difference in total mouse weight, liver or kidney morphology in response to combination treatment (MET+VPA) compared to MET or VPA alone and vehicle control.

CONCLUSION

The combination treatment of MET with VPA is more effective at slowing prostate tumor growth in vivo compared to either drug alone, in mouse xenografts. These pre-clinical results support previous in vitro data and also demonstrate the low toxicity of the combination of these drugs, suggesting that this may be a potential new therapy to be investigated in clinical trials for prostate cancer.

摘要

背景/目的:降糖药物二甲双胍(MET)和抗癫痫药物丙戊酸(VPA)在体外已分别显示出对前列腺癌的抗肿瘤作用。本研究旨在通过临床前异种移植模型研究MET与VPA联合应用在前列腺癌治疗中的疗效。

材料与方法

将前列腺癌细胞系(LNCaP和PC-3)接种于BALB/c裸鼠皮下。给小鼠饮用稀释有200μl/ml MET和/或0.4%(w/v)VPA的水,或给予溶剂对照,并进行监测,直至肿瘤体积达到2000mm³。通过组织学评估药物组合的毒性。

结果

在LNCaP和PC-3异种移植瘤中,与单独使用MET或VPA以及溶剂对照相比,MET与VPA联合应用在治疗后的前4周显著降低了肿瘤生长,并将肿瘤体积达到2000mm³的时间推迟了90天。与单独使用MET或VPA以及溶剂对照相比,联合治疗(MET+VPA)对小鼠总体重、肝脏或肾脏形态没有显著差异。

结论

在小鼠异种移植模型中,与单独使用任何一种药物相比,MET与VPA联合治疗在体内减缓前列腺肿瘤生长方面更有效。这些临床前结果支持了先前的体外数据,也证明了这些药物联合应用的低毒性,表明这可能是一种有待在前列腺癌临床试验中研究的潜在新疗法。

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