Evidence for Bile Acid Synthesis by Transplantable Hepatomas

Glen E. Mott, Henry C. Pitot, Stanley Goldfarb

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

Transplantable Morris hepatomas 5123C and 9618A were assayed for enzymes known to be active in the biosynthesis of bile acids in liver. Cholesterol αa-hydroxylase, the initial enzyme in the pathway of bile acid biosynthesis, was shown to be as active in 9618A tumor microsomes as in host liver microsomes. Activity of this enzyme in the 5123C tumor was about one-third that of host liver. 7α-Hydroxycholesterol was shown to be metabolized by tumor microsomes to other probable intermediates. Cleavage of the sterol side chain, a part of the hepatic bile acid-metabolic pathway, was also detected in both 9618A and 5123C tumor mitochondrial preparations. Labeled chenodeoxycholic acid was identified in extracts from tumor and liver slices that were incubated in the presence of sodium mevalonate- 3 H.

Original languageEnglish (US)
Pages (from-to)1688-1693
Number of pages6
JournalCancer Research
Volume34
Issue number7
StatePublished - Jul 1 1974
Externally publishedYes

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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