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[Cancer Research 48, 1080-1085, March 1, 1988]
© 1988 American Association for Cancer Research

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Vitamin B6 Metabolism in McA-RH7777 Cells1

Natalie T. Meisler and John W. Thanassi2

Department of Biochemistry, University of Vermont College of Medicine, Burlington, Vermont 05405

The metabolism of vitamin B6 in McA-RH7777 cells has been characterized with respect to pyridoxal 5'-phosphate (PLP) levels, and the activities of pyridoxine (PN) kinase (EC 2.1.7.35) and pyridoxine 5'-phosphate (PNP) oxidase (EC 1.4.3.5). PLP levels (12.4 ± 4.4 ng/mg protein) were at the lower end of the range found for Morris hepatomas, carcinogen-induced rat hepatomas, and liver from rats fed a PN-deficient diet. PN kinase activity was about one-third of that found in normal rat liver. PNP oxidase appeared to be absent in high-speed supernatants of homogenates prepared from McA-RH7777 cells. The absence of PNP oxidase was supported by enzymatic and immunological data. These findings resemble those found previously for Morris hepatoma 7777. In contrast to rat liver, such preparations caused little or no release of volatile counts upon incubation with either [3H-C4']PN or [3H-C4']PNP. High-speed supernatants of homogenates prepared from both McA-RH7777 cells and Morris hepatoma 7777 were very much less capable than similar preparations from rat liver in converting [G-3H]PN to PLP and pyridoxamine 5'-phosphate. Despite the apparent absence of PNP oxidase, intact confluent or log-phase McA-RH7777 cells were capable of converting [G-3H]PN to PLP and pyridoxamine 5'-phosphate. These findings are discussed in terms of tumor nutrition and vitamin B6 metabolism in a rat hepatoma cell line.

1 Supported by United States Public Health Service Grant 35878 awarded by the National Cancer Institute, Department of Health and Human Services, and United States Public Health Service Biomedical Research Support Grant 5429-25/16 awarded by the University of Vermont College of Medicine. A preliminary report of this work was presented at the June 1986 meeting of the American Society of Biological Chemists, Washington, DC.

2 To whom requests for reprints should be addressed.

Received 9/21/87. Revised 11/20/87. Accepted 12/ 1/87.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
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Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1988 by the American Association for Cancer Research.