Literature DB >> 4005840

Experimental antitumor activity against murine tumor model systems of 8-carbamoyl-3-(2-chloroethyl)imidazo[5,1-d]-1,2,3,5-tetrazin-4(3 H)-one (mitozolomide), a novel broad-spectrum agent.

J A Hickman, M F Stevens, N W Gibson, S P Langdon, C Fizames, F Lavelle, G Atassi, E Lunt, R M Tilson.   

Abstract

8-Carbamoyl-3-(2-chloroethyl)imidazo[5,1-d]-1,2,3,5-tetrazin-4(3H) -one (mitozolomide) demonstrates curative action against a range of murine tumor model systems. At single doses of between 20 and 40 mg/kg, the latter of which approximates the 10% lethal dose value in mice, the compound elicited cures against the L1210 and P388 leukemias irrespective of the route of tumor and/or drug administration; in these tests, animals receiving 10(5) cells i.p. survived greater than 60 days after treatment. Potent effects were also observed against the TLX5 lymphoma (s.c.) and B16 melanoma (i.p.). In other experiments, 7 of 10 animals implanted with 2 X 10(5) Lewis lung carcinoma cells survived greater than 60 days while 10 of 10 animals survived greater than 60 days after implantation of the Colon 26 tumor. Potent inhibition of the solid tumor models was also observed with complete cures of the Colon 38, M5076 sarcoma, and ADJ/PC6A plasmacytoma. In cross-resistance studies, the compound was ineffective against an L1210 leukemia made resistant to 1,3-bis(2-chloroethyl)-1-nitrosourea and against a TLX5 lymphoma resistant to dimethyltriazenes but cured animals bearing the L1210 leukemia with derived resistance to cyclophosphamide.

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Year:  1985        PMID: 4005840

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  10 in total

1.  Phase I study of mitozolomide on a once daily for 5 days schedule.

Authors:  J H Schornagel; G Simonetti; R Dubbelman; W W ten Bokkel Huinink; J G McVie
Journal:  Cancer Chemother Pharmacol       Date:  1990       Impact factor: 3.333

2.  In vitro and in vivo anticancer activity of mitozolomide and sparsomycin in human tumor xenografts, murine tumors and human bone marrow.

Authors:  H H Fiebig; D P Berger; K Köpping; H C Ottenheijm; Z Zylicz
Journal:  J Cancer Res Clin Oncol       Date:  1990       Impact factor: 4.553

3.  Inhibition of cellular esterases by the antitumour imidazotetrazines mitozolomide and temozolomide: demonstration by flow cytometry and conventional spectrofluorimetry.

Authors:  C Dive; P Workman; J V Watson
Journal:  Cancer Chemother Pharmacol       Date:  1989       Impact factor: 3.333

4.  Activity and distribution studies of etoposide and mitozolomide in vivo and in vitro against human choriocarcinoma cell lines.

Authors:  C J Brindley; R B Pedley; P Antoniw; E S Newlands
Journal:  Cancer Chemother Pharmacol       Date:  1987       Impact factor: 3.333

5.  A clinical and pharmacological study of high-dose mitozolomide given in conjunction with autologous bone marrow rescue.

Authors:  M McKeage; P Dady; M Clear; A MacDonald
Journal:  Cancer Chemother Pharmacol       Date:  1992       Impact factor: 3.333

6.  Mitozolomide-induced sensitisation of mammalian cells in vitro to radiation.

Authors:  M J McKeage; P B Roberts
Journal:  Br J Cancer       Date:  1989-08       Impact factor: 7.640

7.  Phase II evaluation of mitozolomide in ovarian cancer.

Authors:  M Harding; D Northcott; J Smyth; N S Stuart; J A Green; E Newlands
Journal:  Br J Cancer       Date:  1988-01       Impact factor: 7.640

8.  Marked inactivation of O6-alkylguanine-DNA alkyltransferase activity with protracted temozolomide schedules.

Authors:  A W Tolcher; S L Gerson; L Denis; C Geyer; L A Hammond; A Patnaik; A D Goetz; G Schwartz; T Edwards; L Reyderman; P Statkevich; D L Cutler; E K Rowinsky
Journal:  Br J Cancer       Date:  2003-04-07       Impact factor: 7.640

9.  Mitozolomide activity on human cancer cells in vitro.

Authors:  E Erba; S Pepe; P Ubezio; A Lorico; L Morasca; C Mangioni; F Landoni; M D'Incalci
Journal:  Br J Cancer       Date:  1986-12       Impact factor: 7.640

10.  Mitozolomide (NSC 353451), a new active drug in the treatment of malignant melanoma. Phase II trial in patients with advanced disease.

Authors:  S Gundersen; S Aamdal; O Fodstad
Journal:  Br J Cancer       Date:  1987-04       Impact factor: 7.640

  10 in total

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