Oral administration of dihydroartemisinin and ferrous sulfate retarded implanted fibrosarcoma growth in the rat

Cancer Letters

Volumn 98, Issue 1, 1995, Pages 83-87

  Moore, James C ^a   Lai, Henry ^b   Li, Jian Ren ^a   Ren, Ru Long ^a   McDougall, John A ^a   Singh, Narendra P ^b   Chou, Chung Kwang ^a  

^a CITY OF HOPE NATIONAL MEDICAL CENTER   (United States)

^b UNIVERSITY OF WASHINGTON   (United States)

Author keywords

Dihydroartemisinin; Ferrous sulfate; Fibrosarcoma; Oral administration; Tumor growth

Indexed keywords

DIHYDROARTEMISININ; FERROUS SULFATE; FREE RADICAL;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BODY WEIGHT; CANCER INHIBITION; CELL DEATH; CONTROLLED STUDY; CYTOTOXICITY; DRUG SELECTIVITY; FEMALE; FIBROSARCOMA; NONHUMAN; PRIORITY JOURNAL; RAT; TUMOR GROWTH;

ADMINISTRATION, ORAL; ANIMAL; ANTINEOPLASTIC AGENTS, PHYTOGENIC; ANTINEOPLASTIC COMBINED CHEMOTHERAPY PROTOCOLS; FEMALE; FERROUS COMPOUNDS; FIBROSARCOMA; NEOPLASM TRANSPLANTATION; RATS; RATS, INBRED F344; REACTIVE OXYGEN SPECIES; SESQUITERPENES; SUPPORT, U.S. GOV'T, P.H.S.;

ANIMALIA;

EID: 0028865074     PISSN: 03043835     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0304-3835(06)80014-5     Document Type: Article

References (21)

1. Transferrin receptors: structure and function
2. Transferrin receptor: its biological significance
3. Receptor-mediated endocytosis of transferrin in developmentally totipotent mouse teratocarcinoma stem cells
4. Qinghaosu
5. Qinghaosu (artemisinin): an antimalarial drug from China
6. Progress in the research of artemisinin-related antimalarials: an update
7. Hemin-catalyzed decomposition of artemisinin (qinghaosu)
8. Iron-dependent free radical generation from the antimalarial agent artemisinin (qinghaosu)
9. Selective cancer cell cytotoxicity from exposure to dihydroartemisinin and holotransferrin
10. Comparison of in vivo and in vitro antimalarial activity of artemisinin, dihydroartemisinin and sodium artesunate in the Plasmodium berghei-rodent model
11. Nonparametric analysis of response curves
12. Antitumor activities of 4 derivatives of artemisic acid and artemisinin B in vitro
13. Cytotoxicity of artemisinin-related endoperoxides to Ehrlich ascites tumor cells
14. The toxicity of artemisinin and related compounds on neuronal and glial cells in culture
15. Fatal neurotoxicity of arteether and artemether
16. Ro 42-1611 (arteflene), a new effective antimalarial: chemical structure and biological activity
17. Chemotherapy of human carcinoma xenografts during pulsed magnetic field exposure
18. In vitro activity of artemisinin, its derivatives, and pyronaridine against different strains of Plasmodium faliparum
19. Antimalarial activity of new water-soluble dihydroartemisinin derivatives. 3. Aromatic amine analogues
20. The chemotherapy of rodent malaria. XLIX. The activities of some synthetic 1,2,4-trioxanes against chloroquine-sensitive and chloroquine-resistant parasites. Part 2 structure-activity studies on cis-fused cyclopenteno-1,2,4-troxanes (fenozans) against drug-sensitive and drug-resistant lines of Plasmodium berghei and P. yoelii in vivo
21. Extraordinary potent antimalarial compounds: new, structurally simple, easily synthesized, tricyclic 1,2,4 trioxanes