Literature DB >> 8763838

Disruption of normal cellular bioenergetics in Balb/c mice by mitomycin C.

C A Pritsos1, L A Briggs.   

Abstract

Mitomycin C (MMC) is an antineoplastic agent with activity against a wide variety of tumours. The primary cellular target for MMC's antineoplastic activity is thought to be nuclear DNA. The interactions of MMC with nuclear DNA have been studied extensively. This laboratory has shown recently that MMC also interacts with mitochondrial DNA, resulting in a conformational change from the supercoiled to the relaxed state. This interaction could cause mitochondrial dysfunction, resulting in a loss of cellular ATP. The present studies were designed to test whether treatment with MMC would affect tissue ATP levels in Balb/c mice. Mice were treated with single, or multiple (2) i.p. injections of 0, 5, 10 or 20 mg MMC kg-1 body wt. Forty-eight hours after the final MMC treatment, heart, liver and kidney tissues were excised and tissue ATP levels were assessed. Heart tissue was the most sensitive to the MMC treatment and significant decreases in ATP levels were observed at all MMC dosages tested. Liver and kidney tissues showed significant decreases only at the highest dosages tested. These studies demonstrate that tissue specific disruption of cellular bioenergetics occurs following MMC exposure resulting in a decrease of tissue ATP levels.

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Year:  1996        PMID: 8763838      PMCID: PMC2150021     

Source DB:  PubMed          Journal:  Br J Cancer Suppl        ISSN: 0306-9443


  15 in total

1.  A general mechanism for microsomal activation of quinone anticancer agents to free radicals.

Authors:  N R Bachur; S L Gordon; M V Gee
Journal:  Cancer Res       Date:  1978-06       Impact factor: 12.701

2.  The elucidation of the human mitochondrial genome: a historical perspective.

Authors:  G Attardi
Journal:  Bioessays       Date:  1986-07       Impact factor: 4.345

3.  Biospecific adsorption of hepatic DT-diaphorase on immobilized dicoumarol. II. Purification of mitochondrial and microsomal DT-diaphorase from 3-methylcholanthrene-treated rats.

Authors:  C Lind; B Höjeberg
Journal:  Arch Biochem Biophys       Date:  1981-03       Impact factor: 4.013

4.  Mitomycin C-enhanced superoxide and hydrogen peroxide formation in rat heart.

Authors:  J H Doroshow
Journal:  J Pharmacol Exp Ther       Date:  1981-07       Impact factor: 4.030

5.  Distinctive features of the 5'-terminal sequences of the human mitochondrial mRNAs.

Authors:  J Montoya; D Ojala; G Attardi
Journal:  Nature       Date:  1981-04-09       Impact factor: 49.962

6.  Isolation and structure of a covalent cross-link adduct between mitomycin C and DNA.

Authors:  M Tomasz; R Lipman; D Chowdary; J Pawlak; G L Verdine; K Nakanishi
Journal:  Science       Date:  1987-03-06       Impact factor: 47.728

7.  Sequence and gene organization of mouse mitochondrial DNA.

Authors:  M J Bibb; R A Van Etten; C T Wright; M W Walberg; D A Clayton
Journal:  Cell       Date:  1981-10       Impact factor: 41.582

8.  MITOMYCINS AND PORFIROMYCIN: CHEMICAL MECHANISM OF ACTIVATION AND CROSS-LINKING OF DNA.

Authors:  V N IYER; W SZYBALSKI
Journal:  Science       Date:  1964-07-03       Impact factor: 47.728

9.  Redox cycling of anthracyclines by cardiac mitochondria. I. Anthracycline radical formation by NADH dehydrogenase.

Authors:  K J Davies; J H Doroshow
Journal:  J Biol Chem       Date:  1986-03-05       Impact factor: 5.157

10.  Anthracycline antibiotic-stimulated superoxide, hydrogen peroxide, and hydroxyl radical production by NADH dehydrogenase.

Authors:  J H Doroshow
Journal:  Cancer Res       Date:  1983-10       Impact factor: 12.701

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