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环缩肽(FK228)抑制人前列腺癌细胞的生长。

Depsipeptide (FK228) inhibits growth of human prostate cancer cells.

作者信息

Lai Ming-Tsung, Yang Chuan-Ching, Lin Tsai-Yun, Tsai Fuu-Jen, Chen Wen-Chi

机构信息

Department of Life Science, National Tsing Hua University, Hsinchu, Taiwan.

出版信息

Urol Oncol. 2008 Mar-Apr;26(2):182-9. doi: 10.1016/j.urolonc.2007.01.020. Epub 2007 Nov 19.

DOI:10.1016/j.urolonc.2007.01.020
PMID:18312939
Abstract

FK228 (depsipeptide) is a natural prodrug that inhibits class I histone deacetylases. We aimed to investigate the effects FK228 has on prostate cancer cells in vivo. In non-obese diabetic-severe combined immunodeficient mice implanted with human prostate cancer cells, 50 mg/kg FK228 given orally 3 times a week inhibited tumor growth and metastasis. The median time to the experimental end point (tumor volume 2 cm(3) or death) in the untreated group was 52 days, and average tumor volume was 0.8 +/- 0.18 cm(3). At the same time, 94.4% of FK228-treated mice survived and had average tumor volumes of 0.37 +/- 0.1 cm(3). All untreated animals died at 98 days, whereas, 61% of treated animal remained alive. Sizeable metastatic tumors positively stained for prostate-specific antigen (PSA), and limited air gaps were found in the lungs of untreated mice. In animals treated with FK228, lung morphology appeared normal. Primary tumors of treated animals were highly positive for PSA, and had an increased level of p21 and the proapoptotic protein Bax. Sections taken from FK228-treated animals and examined under an electron microscope showed condensed chromatin and apoptotic bodies. PSA serum levels were higher in untreated than in treated animals and correlated with tumor volume. Because prolonged oral administration of 50 mg/kg or a single oral dose of 1.2 g/kg FK228 did not cause adverse effects and inhibited proliferation of human prostate cancer cells in vivo, FK228 likely has a potential anticancer effect for prostate cancer.

摘要

FK228(缩肽)是一种抑制I类组蛋白去乙酰化酶的天然前体药物。我们旨在研究FK228对体内前列腺癌细胞的影响。在植入人前列腺癌细胞的非肥胖糖尿病-严重联合免疫缺陷小鼠中,每周口服3次50mg/kg的FK228可抑制肿瘤生长和转移。未治疗组达到实验终点(肿瘤体积2cm³或死亡)的中位时间为52天,平均肿瘤体积为0.8±0.18cm³。同时,接受FK228治疗的小鼠中有94.4%存活,平均肿瘤体积为0.37±0.1cm³。所有未治疗的动物在98天时死亡,而接受治疗的动物中有61%仍存活。大量转移瘤前列腺特异性抗原(PSA)染色呈阳性,未治疗小鼠的肺中发现有限的气隙。在用FK228治疗的动物中,肺形态正常。接受治疗动物的原发性肿瘤PSA高度阳性,p21和促凋亡蛋白Bax水平升高。取自接受FK228治疗动物的切片在电子显微镜下检查显示染色质浓缩和凋亡小体。未治疗动物的PSA血清水平高于接受治疗的动物,且与肿瘤体积相关。由于长期口服50mg/kg或单次口服1.2g/kg的FK228不会引起不良反应且可抑制体内人前列腺癌细胞的增殖,FK228可能对前列腺癌具有潜在的抗癌作用。

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