Literature DB >> 17826527

Enhanced therapeutic effect on androgen-independent prostate cancer by depsipeptide (FK228), a histone deacetylase inhibitor, in combination with docetaxel.

Zhengwang Zhang1, Jennifer Stanfield, Eugene Frenkel, Wareef Kabbani, Jer-Tsong Hsieh.   

Abstract

OBJECTIVES: To study whether a histone deacetylase inhibitor, FK228, can enhance therapeutic efficacies of other chemotherapeutic agents against androgen-independent prostate cancer (AIPCa) and to explore any possible early biomarker for predicting drug response.
METHODS: The therapeutic effects of FK228-based combinations on three AIPCa cell lines (PC-3, DU145, and C4-2) were evaluated by synergisms of cytotoxicity. Cell cycle analysis and Western blot assay were used to study the underlying mechanisms of drug action and search for any potential surrogate biomarker. In addition, we investigated the in vivo antitumor effects of the FK228/docetaxel combination using the PC-3 xenograft model.
RESULTS: FK228/docetaxel surpassed other FK228-based combinations by achieving more synergism of cytotoxicity. FK228 enhanced the therapeutic effect of docetaxel against AIPCa by exhibiting markedly enhanced and prolonged inhibitory effects in vitro and better tumor regression in vivo by inducing apoptosis. It appears that p21(WAF1) induction consistently correlates with single or combination treatment.
CONCLUSIONS: The results of our study have shown that FK228 is able to enhance the therapeutic effect of docetaxel against AIPCa. FK228 appears to be a promising second-line option in combination with docetaxel. The p21(WAF1) protein level can be used as a surrogate biomarker to predict and monitor the therapeutic response.

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Year:  2007        PMID: 17826527     DOI: 10.1016/j.urology.2007.03.052

Source DB:  PubMed          Journal:  Urology        ISSN: 0090-4295            Impact factor:   2.649


  7 in total

1.  The HDAC inhibitor FK228 enhances adenoviral transgene expression by a transduction-independent mechanism but does not increase adenovirus replication.

Authors:  Angelika Danielsson; Helena Dzojic; Victoria Rashkova; Wing-Shing Cheng; Magnus Essand
Journal:  PLoS One       Date:  2011-02-17       Impact factor: 3.240

2.  Phase II trial of the histone deacetylase inhibitor romidepsin in patients with recurrent/metastatic head and neck cancer.

Authors:  Missak Haigentz; Mimi Kim; Catherine Sarta; Juan Lin; Roger S Keresztes; Bruce Culliney; Anu G Gaba; Richard V Smith; Geoffrey I Shapiro; Lucian R Chirieac; John M Mariadason; Thomas J Belbin; John M Greally; John J Wright; Robert I Haddad
Journal:  Oral Oncol       Date:  2012-06-28       Impact factor: 5.337

3.  A novel histone deacetylase inhibitor, CG200745, potentiates anticancer effect of docetaxel in prostate cancer via decreasing Mcl-1 and Bcl-XL.

Authors:  Jung Jin Hwang; Yong Sook Kim; Taelim Kim; Mi Joung Kim; In Gab Jeong; Je-Hwan Lee; Jene Choi; Sejin Jang; Seonggu Ro; Choung-Soo Kim
Journal:  Invest New Drugs       Date:  2011-07-20       Impact factor: 3.850

4.  Prostate-cancer-targeted N-(2-hydroxypropyl)methacrylamide copolymer/docetaxel conjugates.

Authors:  Jihua Liu; Pavla Kopečková; Huaizhong Pan; Monika Sima; Patrick Bühler; Philipp Wolf; Ursula Elsässer-Beile; Jindřich Kopeček
Journal:  Macromol Biosci       Date:  2012-03       Impact factor: 4.979

5.  Adenoviral-mediated pHyde gene transfer and cisplatin additively inhibit human prostate cancer growth by enhancing apoptosis.

Authors:  Yi Lu; Xiongwen Zhang; Ben Beheshti; Jun Zhang
Journal:  Prostate       Date:  2009-02-15       Impact factor: 4.104

6.  Epigenetic regulation of prostate cancer.

Authors:  Suyin P Chin; Joanne L Dickinson; Adele F Holloway
Journal:  Clin Epigenetics       Date:  2011-06-14       Impact factor: 6.551

Review 7.  Epigenetic modulators as therapeutic targets in prostate cancer.

Authors:  Inês Graça; Eva Pereira-Silva; Rui Henrique; Graham Packham; Simon J Crabb; Carmen Jerónimo
Journal:  Clin Epigenetics       Date:  2016-09-15       Impact factor: 6.551

  7 in total

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