Depsipeptide (FK228) inhibits growth of human prostate cancer cells

• Published in: Urologic oncology 2008-03, Vol.26 (2), p.182-189
• Main Authors: Lai, Ming-Tsung, M.D., Ph.D, Yang, Chuan-Ching, Ph.D, Lin, Tsai-Yun, Ph.D, Tsai, Fuu-Jen, M.D., PhD, Chen, Wen-Chi, M.D., Ph.D
• Format: Article
• Language: English
• Subjects: Animals; Antibiotics, Antineoplastic - pharmacology; Biological and medical sciences; Cell Line, Tumor; Cell Proliferation - drug effects; Depsipeptides - pharmacology; Drug Screening Assays, Antitumor; FK228; Histone deacetylase inhibitor; Humans; Lung metastasis; Male; Medical sciences; Mice; Nephrology. Urinary tract diseases; Prodrug; Prostate adenocarcinoma; Prostate-specific antigen; Prostatic Neoplasms - pathology; Prostatic Neoplasms - prevention & control; Tumors; Tumors of the urinary system; Urinary tract. Prostate gland; Urology
• ISSN: 1078-1439; 1873-2496
• DOI: 10.1016/j.urolonc.2007.01.020

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 cm3 or death) in the untreated group was 52 days, and average tumor volume was 0.8 ± 0.18 cm3 . At the same time, 94.4% of FK228-treated mice survived and had average tumor volumes of 0.37 ± 0.1 cm3 . 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.