Abstract:
:Inhibitors of polyamine synthesis were tested for therapeutic effectiveness on transplantable prostate cancer. Inhibition of either ornithine decarboxylase or S-adenosyl-L-methionine decarboxylase (AMDC) by alpha-difluormethylornithine (DFMO) or methylglyoxal-bis[guanylhydrazone] (MGBG), respectively, was associated with significant antitumor effect. The combination of DFMO with MGBG was not only more effective but no more toxic than MGBG alone. Combination of MGBG with 9-B-D-arabinofuranosyladenine, an indirect effector of SAMDC, failed to increase therapeutic effectiveness of MGBG.
journal_name
Oncologyjournal_title
Oncologyauthors
Dunzendorfer U,Relyea NM,Kleinert E,Balis ME,Whitmore WF Jrdoi
10.1159/000225692subject
Has Abstractpub_date
1983-01-01 00:00:00pages
57-62issue
1eissn
0030-2414issn
1423-0232journal_volume
40pub_type
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