Methionine synthase activity and sulphur amino acid levels in the rat liver tumour cells HTC and Phi-1

Susan H. Kenyon, Catherine J. Waterfield, John A. Timbrell, Anna Nicolaou

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Methionine dependence has been reported in tumour cells and suggested as a possible target for chemotherapeutic drugs. The underlying defect has not been extensively researched, nor have levels of sulphur amino acids been examined in these cells. This study compared two rat liver tumour cell lines. One was found to be methionine dependent (HTC) and the other found to be methionine independent (Phi-1). The methionine-dependent cell line (HTC) was discovered to contain markedly less methionine synthase activity, the enzyme activity being less responsive to methionine concentration than in the methionine-independent cells (Phi-1). HTC cells had lower cysteine requirements and contained larger concentrations of reduced glutathione (GSH) and taurine than the Phi-1 cells. Also, in contrast to Phi-1 cells, no glutathione was found in the media of the HTC cells, although large quantities of cysteinylglycine were detected. These results suggested that differences in methionine synthase activity might be partly responsible for methionine dependence and that methionine-dependent cells may have different metabolic requirements for other sulphur amino acids. © 2002 Elsevier Science Inc. All rights reserved.
    Original languageEnglish
    Pages (from-to)381-391
    Number of pages10
    JournalBiochemical Pharmacology
    Volume63
    Issue number3
    Publication statusPublished - 1 Feb 2002

    Keywords

    • Cysteine
    • Glutathione
    • Hepatocytes
    • Homocysteine
    • Methionine dependence
    • Methionine synthase
    • Taurine
    • Tumour cell

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