Abstract |
The purpose of this study was to investigate the potential use of PET in vivo to record cytotoxic effects of 2-methoxyestradiol (2-ME), an endogenous metabolite of 17beta-estradiol. The anti-proliferative and pro-apoptotic effects of 2-ME on human prostate cancer cell (PC3) aggregates in vitro, were correlated with the uptake of fluoro-deoxy- D-glucose, FMAU and choline labelled with 18F, 11C, or 3H. 2-ME clearly reduced growth of PC3 aggregates and induced apoptosis in a dose-dependent manner. However, the uptake of the putative proliferation markers 11C-FMAU or 3H-choline failed to record the growth inhibitory effects of 2-ME on PC3 cell aggregates. The uptake of 18F-FDG was used as a marker for effects on cellular metabolism and also failed to show any dose-dependent effects in PC3 aggregates. The use of these PET-tracers in vivo is therefore not recommended in order to evaluate the cytotoxic effects of 2-ME on human prostate cancer cells.
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Authors | Padideh Davoodpour, Mats Bergström, Maréne Landström |
Journal | Nuclear medicine and biology
(Nucl Med Biol)
Vol. 31
Issue 7
Pg. 867-74
(Oct 2004)
ISSN: 0969-8051 [Print] United States |
PMID | 15464388
(Publication Type: Comparative Study, Evaluation Study, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antineoplastic Agents
- Radioisotopes
- Radiopharmaceuticals
- Estradiol
- 2-Methoxyestradiol
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Topics |
- 2-Methoxyestradiol
- Antineoplastic Agents
(administration & dosage)
- Apoptosis
(drug effects)
- Cell Aggregation
(drug effects)
- Cell Line, Tumor
- Cell Proliferation
(drug effects)
- Dose-Response Relationship, Drug
- Estradiol
(administration & dosage, analogs & derivatives)
- Humans
- Male
- Neoplasm Staging
(methods)
- Positron-Emission Tomography
(methods)
- Prostatic Neoplasms
(diagnostic imaging, drug therapy, metabolism, pathology)
- Radioisotopes
(pharmacokinetics)
- Radiopharmaceuticals
(pharmacokinetics)
- Reproducibility of Results
- Sensitivity and Specificity
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