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Proteome analysis of chemically induced mouse liver tumors with different genotype.

Proteome analysis of chemically induced mouse liver tumors with different genotype. Research Abstract Details 

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  • Proteome analysis of chemically induced mouse liver tumors with different genotype. Abstract Text:

    julia strathmannJulia Strathmann,krisztina paalKrisztina Paal,carina ittrichCarina Ittrich,eberhard krauseEberhard Krause,klaus e appelKlaus E Appel,howard p glauertHoward P Glauert,albrecht buchmannAlbrecht Buchmann,michael schwarzMichael Schwarz,

    Mouse liver tumors frequently harbor mutations in Ha-ras, B-raf, or Ctnnb1 (encoding beta-catenin). We conducted a proteome analysis with protein extracts from normal mouse liver and from liver tumors which were induced by a single injection of N-nitrosodiethylamine (DEN) as initiator followed by multiple injections of two different polychlorinated biphenyls (PCBs) as tumor promoters, or corn oil as a control. Liver tumors were stratified into two classes: they were either mutated in Ctnnb1 and positive for the marker glutamine synthetase (GS(+)), or they lacked Ctnnb1 mutations and were therefore GS-negative (GS(-)). Proteome analysis by 2-DE and MS revealed 98 significantly deregulated proteins, 44 in GS(+) and 54 in GS(-) tumors. Twelve of these proteins showed expression changes in both tumor types, but only seven of them were deregulated in the same direction. Several of the identified enzymes could be assigned to fundamental metabolic or other cellular pathways with characteristically different alterations in GS(+) and GS(-) tumors such as ammonia and amino acid turnover, cellular energy supply, and calcium homeostasis. Our data suggest that GS(+) and GS(-) tumor cells show a completely different biology and use divergent evolutionary strategies to gain a selective advantage over normal hepatocytes.

    Proteome analysis of chemically induced mouse liver tumors with different genotype. Publishing Authors By Initials

    j strathmannJ Strathmann,k paalK Paal,c ittrichC Ittrich,e krauseE Krause,ke appelKE Appel,hp glauertHP Glauert,a buchmannA Buchmann,m schwarzM Schwarz,

    For similar proteins: proteome research abstracts see: proteins: proteome research

    PUBMED ID PMID:

    MEDLINE DATE:

    Proteome analysis of chemically induced mouse liver tumors with different genotype. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Proteomics

    VOLUME: 7

    Page Numbers: 3318-31

    Journal Abbreviation: Proteomics

    ISSN: 1615-9853

    DAY: 3

    MONTH: Sep

    YEAR: 2007

    Proteome analysis of chemically induced mouse liver tumors with different genotype. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 101092707

    Proteome analysis of chemically induced mouse liver tumors with different genotype. Keywords Mesh Terms:

    KEYWORDS: Proteome

    MESH TERMS: toxicity

    Chemical & Substance for Abstract: Proteome analysis of chemically induced mouse liver tumors with different genotype. Information

    Substance Name: Proteome

    Registry Number: 0

    Grant and Affiliation Information for Proteome analysis of chemically induced mouse liver tumors with different genotype.

    AFFILIATION: Department of Toxicology, University of Tübingen, Tübingen, Germany.

    Country: Germany

    Germany Research PublicationGermany Research Publication

    AGENCY: United States NIEHS

    GRANT: ES-07380

    ACRONYM: ES

    MEDLINETA: Proteomics

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

    Number Hits: 0

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