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Vitamin B6 metabolism in liver and liver-derived tumors.

Abstract
Vitamin B6 metabolism has been investigated in several highly and well-differentiated Morris hepatomas. Comparisons have been made with two poorly differentiated Morris hepatomas, with host livers obtained from tumor-bearing animals, and with fetal, neonatal, and adult rat liver. The pyridoxal phosphate content and the activities of pyridoxine kinase and pyridoxine phosphate oxidase of all Morris hepatomas examined were significantly less than those in adult host or control livers and generally fell in the range determined for fetal and neonatal liver. A similar pattern was not evident for the activity of pyridoxine phosphate phosphatase. Relative to control and host livers, the activity in hepatomas of the pyridoxal phosphate (PLP)-dependent enzyme, ornithine decarboxylase, was generally elevated. Dexamethasone, at a dose which caused an elevation in the activity of PLP-dependent tumor tyrosine aminotransferase, had no effect on PLP metabolism. The data indicate that tumor progression in the Morris hepatoma spectrum in relation to vitamin b6 metabolism falls into an onco-developmental pattern characterized by a diminished amount of tissue PLP and a diminished capability to metabolize precursor vitamer forms to PLP.
AuthorsN T Meisler, L M Nutter, J W Thanassi
JournalCancer research (Cancer Res) Vol. 42 Issue 9 Pg. 3538-43 (Sep 1982) ISSN: 0008-5472 [Print] United States
PMID6125259 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Pyridoxal Phosphate
  • Dexamethasone
  • Pyridoxaminephosphate Oxidase
  • Tyrosine Transaminase
  • Pyridoxal Kinase
  • pyridoxine phosphate phosphatase
  • Phosphoric Monoester Hydrolases
  • Ornithine Decarboxylase
  • Pyridoxine
Topics
  • Animals
  • Dexamethasone (pharmacology)
  • Female
  • Liver (embryology, metabolism)
  • Liver Neoplasms, Experimental (enzymology, metabolism)
  • Ornithine Decarboxylase (metabolism)
  • Phosphoric Monoester Hydrolases (metabolism)
  • Pyridoxal Kinase (metabolism)
  • Pyridoxal Phosphate (metabolism)
  • Pyridoxaminephosphate Oxidase (metabolism)
  • Pyridoxine (metabolism)
  • Rats
  • Rats, Inbred BUF
  • Tyrosine Transaminase (metabolism)

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