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Effects of new bisphosphonic acids on tumor-induced bone destruction in the rat.

Abstract
This report is concerned with therapeutic studies utilizing new bisphosphonic acids on tumor-induced osteolytic metastases. The bone metastases on SD rats were induced by intraarterial and intraosseous transplantation of Walker carcinosarcoma 256 B ascites cells. The treatment was carried out using disodium-3-amino-1-hydroxypropylidene-1,1-bisphosphonate (ADP), diglycidyl-[3-(3, 3-bisphosphono-3-hydroxy-propylamino)-2-hydroxypropyl-]urazol++ +-Na2 (DDU) and 1,2,4-triglycidylurazol (TGU). The extent of bone metastases was determined by X-ray on the 5th and 10th days following tumor inoculation, as well as both microradiographically and histologically upon termination of the experiment. High dose DDU produced a clear reduction of the tumor osteolysis, but these positive results were surpassed using APD. The best results were achieved by pretreatment with APD 24 h prior to tumor inoculation.
AuthorsF Wingen, T Eichmann, C Manegold, B Krempien
JournalJournal of cancer research and clinical oncology (J Cancer Res Clin Oncol) Vol. 111 Issue 1 Pg. 35-41 ( 1986) ISSN: 0171-5216 [Print] Germany
PMID3949849 (Publication Type: Journal Article)
Chemical References
  • Antineoplastic Agents
  • Diphosphonates
  • Organophosphonates
  • Organophosphorus Compounds
  • Triazoles
  • diglycidyl-(3-(3,3-bisphosphono-3-hydroxypropylamino)-2-hydroxypropyl)urazol
  • anaxirone
  • Pamidronate
Topics
  • Animals
  • Antineoplastic Agents
  • Bone Neoplasms (drug therapy, metabolism, secondary)
  • Carcinoma 256, Walker (drug therapy, metabolism, secondary)
  • Diphosphonates (metabolism, therapeutic use)
  • Male
  • Organophosphonates (metabolism, therapeutic use)
  • Organophosphorus Compounds (metabolism, therapeutic use)
  • Pamidronate
  • Rats
  • Time Factors
  • Triazoles (metabolism, therapeutic use)

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