## Abstract The purpose of this study was to assess the relationship between progression‐free survival (PFS) in patients treated with DFMO + PCV (procarbazine, CCNU, vincristine) chemotherapy for malignant gliomas with tumor cell ornithine decarboxylase (ODC) activity. Formalin‐fixed slides were ob
Ornithine decarboxylase activity in tumor: A study with L-[1–14C]- and L-[5–14C]-ornithine
✍ Scribed by Ph.H. Elsinga; B.J.G. Daemen; W. Vaalburg
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- French
- Weight
- 114 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
The aim of this study is to investigate the possibility to measure ornithine decarboxylase (ODC) activity by PET. From the metabolic pathways of L-ornithine (fig. 1) can be concluded that the difference in uptake of L-[l-l4C]-ornithine (L-1-orn) and L-[5-14C]-ornithine (L-5-orn) may reflect the ODC-activity, assuming that 14C02 is cleared from the tissue rapidly. Decarboxylation of L-ornithine forming putrescine is the initial and rate limiting step to polyamine biosynthesis (1).
Polyamine levels and ODC-activity are increased in many rapid growing tissues like tumors (2). D,L-1-orn is applied in animals and patients to measure the decarboxylation by ODC both in vitro and in vivo (3). D,L-[1-11CI-ornithine is shown to accumulate in tumors (4), while D,L-5-orn is used as a marker of polyamine levels in tissues.
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