Anti-tumor efficacy of glutaminase-copper-ATP combination in mice bearing Ehrlich ascites carcinoma.

Abstract

Glutaminase is a hematotoxic anti-tumor agent, and copper-ATP complex (Cu-ATP) is both anti-neoplastic and hematostimulatory. Combination chemotherapy with these two agents has been performed in mice bearing Ehrlich ascites carcinoma, to elucidate whether this could result in augmented tumor inhibition with reduced hematotoxicity. Glutaminase-Cu-ATP combination (glutaminase 250 IU/kg per day intraperitoneally for 10 days and Cu-ATP 2.5 mg/kg per day intraperitoneally for 10 days) was observed to be more effective in inhibiting tumor growth and in increasing the life span of the tumor hosts, compared with the individual efficacies of these two agents. Moreover, addition of Cu-ATP successfully prevented the hematotoxic effects of glutaminase in normal and in tumor-bearing animals. Thus glutaminase in combination with Cu-ATP holds promise for an effective cancer chemotherapeutic regimen.

• Authors: S Pal, P Maity
• Journal: Anti-cancer drugs (Anticancer Drugs) Vol. 5 Issue 1 Pg. 57-63 (Feb 1994) ISSN: 0959-4973 [Print] England
• PMID: 8186431 (Publication Type: Journal Article)

Chemical References

• DNA, Neoplasm
• Neoplasm Proteins
• RNA, Neoplasm
• Copper
• Adenosine Triphosphate
• Glutaminase

Topics

• Adenosine Triphosphate (administration & dosage)
• Animals
• Antineoplastic Combined Chemotherapy Protocols (adverse effects, pharmacology)
• Blood Cell Count (drug effects)
• Bone Marrow (drug effects, pathology)
• Carcinoma, Ehrlich Tumor (drug therapy, metabolism, pathology)
• Cell Nucleus (drug effects)
• Colony-Forming Units Assay
• Copper (administration & dosage)
• DNA, Neoplasm (biosynthesis)
• Drug Synergism
• Glutaminase (administration & dosage, metabolism)
• Liver (enzymology)
• Male
• Mice
• Neoplasm Proteins (biosynthesis)
• Neoplasm Transplantation
• RNA, Neoplasm (biosynthesis)
• Spleen (drug effects, pathology)