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.
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Authors | F Wingen, T Eichmann, C Manegold, B Krempien |
Journal | Journal of cancer research and clinical oncology
(J Cancer Res Clin Oncol)
Vol. 111
Issue 1
Pg. 35-41
( 1986)
ISSN: 0171-5216 [Print] Germany |
PMID | 3949849
(Publication Type: Journal Article)
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Chemical References |
- Antineoplastic Agents
- Diphosphonates
- Organophosphonates
- Organophosphorus Compounds
- Triazoles
- diglycidyl-(3-(3,3-bisphosphono-3-hydroxypropylamino)-2-hydroxypropyl)urazol
- anaxirone
- Pamidronate
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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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