In vitro and in vivo effects of easily administered, low-toxic retinoid and phenylacetate compounds on human neuroblastoma cells

• Type of Material: Article
• Authors: Neil Sidell, Emory University; M. Pasquali, University of Utah; S. Malkapuram, Emory University; A.B. Barua, Iowa State University; T. Wanichkul, Emory University; R.K. Wada, Cancer Research Center of Hawaii
• Language: English
• Date: 2003-07-21
• Publisher: Cancer Research UK
• Publication Version: Final Published Version
• Copyright Statement: © 2003 Cancer Research UK
• License: Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported
• Final Published Version (URL): http://www.nature.com/bjc/journal/v89/n2/full/6601108a.html
• Title of Journal or Parent Work: British Journal of Cancer
• ISSN: 0007-0920
• Volume: 89
• Issue: 2
• Start Page: 412
• End Page: 419
• Grant/Funding Information: This work was supported by NIH Grants CA43503, CA85589, HD40932 (NS), DK39733 (ABB), and NS34432 (RKW).
• Keywords: neuroblastoma; retinoyl glucuronide; phenylacetate; chemoprevention
• Research Categories: Health Sciences, Oncology; Health Sciences, Obstetrics and Gynecology

Abstract

We have investigated the effects of the low-toxic retinoid, all-trans retinoyl β-glucuronide (RAG) alone and in combination with the phenylacetate (PA) derivative 4-chloro-phenylacetate (4-CPA) on the human neuroblastoma cell line, LA-N-5. In vitro studies demonstrated that RAG and 4-CPA treatments alone showed differentiation-inducing activity on LA-N-5 cells, with 4-CPA found to be about three-fold more potent than the PA parent compound in inducing morphologic differentiation and growth inhibition. As previously reported for retinoic acid (RA) and PA, RAG and 4-CPA were significantly more effective in their antiproliferative effects on the cells than either agent alone. Pharmacologic studies of 4-CPA in mice demonstrated that blood plasma levels reached peak concentrations 4 h after bolus administration of the compound and showed slow clearance characteristics with an apparent half-life of 4–8 h. As opposed to PA, 4-CPA was found to be essentially odourless and readily consumed in drinking water, giving rise to steady-state blood plasma levels of 4-CPA in the near mM range. Continuous consumption of 4-CPA in this manner for up to 5 months demonstrated no apparent adverse effects on the mice. Long-term RAG- and/or 4-CPA-treatment of nude mice injected with LA-N-5 cells demonstrated that both compounds alone exhibit potent antitumour activity. Together, RAG plus 4-CPA was the most effective treatment for inhibiting established tumour growth. In contrast, 4-CPA alone was equally as effective as the combination for preventing tumour development. The potent in vivo antitumour effects of 4-CPA could not be accounted for by the known ability of PA compounds to induce expression of the RA nuclear receptor beta (RARβ) suppressor gene. Taken together, these findings demonstrate the possibility that RAG and/or 4-CPA may serve as effective, less-toxic alternatives to 13-cis RA, which is presently being utilised for nb therapy.