HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Damages of DNA synthesis in normal and tumor cells with sugar alcohol derivatives.

Abstract
The rates of incorporation of 2-14C-thymidine into DNA of melanoma B16, bone marrow, gastrointestinal mucosa, spleen and liver at various time after administration of dianhydrogalactitol (DAG), 3,4-diacetyldianhydrogalactitol (DiacDAG) and 3,4-disuccinyldianhydrogalactitol (DisuDAG) at maxima nonlethal single doses to tumor-bearing mice were studied. The sugar alcohol derivatives induced the stable inhibition in DNA synthesis of tumor cells. DNA synthesis in normal dividing cells was shown to recover more rapidly than in melanoma B16 cells after administration of all drugs. DisuDAG is characterized by stronger inhibitory effect on DNA synthesis in melanoma B16 cells at the half of the single maxima nonlethal dose compared with DAG and DiacDAG. Differing from DAG, DiacDAG and DisuDAG did not effect the incorporation of 2-14C-thymidine into DNA of liver cells. In vivo inhibition of DNA synthesis in melanoma B16 cells with DiacDAG was not due to damage of the TCA soluble fraction.
AuthorsI S Sokolova, I Elekes, L Otvös, L B Gorbacheva
JournalNeoplasma (Neoplasma) Vol. 31 Issue 6 Pg. 667-73 ( 1984) ISSN: 0028-2685 [Print] Slovakia
PMID6521797 (Publication Type: Comparative Study, Journal Article)
Chemical References
  • Antineoplastic Agents
  • Sugar Alcohols
  • Dianhydrogalactitol
  • dianhydro-3,4-diacetylgalactitol
  • 3,4-disuccinyl 1,2-5,6-dianhydrogalactitol
  • DNA
  • Thymidine
Topics
  • Animals
  • Antineoplastic Agents (adverse effects, therapeutic use)
  • Bone Marrow (metabolism)
  • Cell Line
  • DNA (biosynthesis)
  • Dianhydrogalactitol (analogs & derivatives, therapeutic use)
  • Injections, Intraperitoneal
  • Melanoma (drug therapy, pathology)
  • Mice
  • Mice, Inbred Strains
  • Mucous Membrane (metabolism)
  • Spleen (metabolism)
  • Sugar Alcohols (adverse effects, therapeutic use)
  • Thymidine (metabolism)
  • Time Factors

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: