HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Effects of 2-methoxyestradiol on proliferation, apoptosis and PET-tracer uptake in human prostate cancer cell aggregates.

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.
AuthorsPadideh Davoodpour, Mats Bergström, Maréne Landström
JournalNuclear medicine and biology (Nucl Med Biol) Vol. 31 Issue 7 Pg. 867-74 (Oct 2004) ISSN: 0969-8051 [Print] United States
PMID15464388 (Publication Type: Comparative Study, Evaluation Study, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antineoplastic Agents
  • Radioisotopes
  • Radiopharmaceuticals
  • Estradiol
  • 2-Methoxyestradiol
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

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: