Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/22799
Title: Recombinant human arginase inhibits proliferation of human hepatocellular carcinoma by inducing cell cycle arrest
Authors: Lam, TL
Wong, GKY
Chong, HC
Cheng, PNM
Choi, SC
Chow, TL
Kwok, SY
Poon, RTP
Wheatley, DN
Lo, WH 
Leung, YC 
Keywords: Hepatocellular carcinoma (HCC)
Recombinant human arginase
Ornithine transcarbamylase
G2/M phase arrest
Combination therapy
Issue Date: 2009
Source: Cancer letters, 2009, v. 277, no. 1, p. 91-100 How to cite?
Journal: Cancer letters 
Abstract: Human hepatocellular carcinoma (HCC) has an elevated requirement for arginine in vitro, and pegylated recombinant human arginase I (rhArg-PEG), an arginine-depleting enzyme, can inhibit the growth of arginine-dependent tumors. While supplementation of the culture medium with ornithine failed to rescue Hep3B cells from growth inhibition induced by rhArg-PEG, citrulline successfully restored cell growth. The data support the roles previously proposed for ornithine transcarbamylase (OTC) in the arginine auxotrophy and rhArg-PEG sensitivity of HCC cells. Expression profiling of argininosuccinate synthetase (ASS), argininosuccinate lyase (ASL) and OTC in 40 HCC tumor biopsy specimens predicted that 16 of the patients would be rhArg-sensitive, compared with 5 who would be sensitive to arginine deiminase (ADI), another arginine-depleting enzyme with anti-tumor activity. Furthermore, rhArg-PEG-mediated deprivation of arginine from the culture medium of different HCC cell lines produced cell cycle arrests at the G2/M or S phase, possibly mediated by transcriptional modulation of cyclins and/or cyclin dependent kinases (CDKs). Based on these results, together with further validation of the in vivo efficacy of rhArg-PEG against HCC, we propose that the application of rhArg-PEG alone or in combination with existing chemotherapeutic drugs may represent a specific and effective therapeutic strategy against HCC.
URI: http://hdl.handle.net/10397/22799
ISSN: 0304-3835
DOI: 10.1016/j.canlet.2008.11.031
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