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Tricarboxylic acid cycle dysfunction as a cause of human diseases and tumor formation.

Authors
  • Brière, Jean-Jacques
  • Favier, Judith
  • Gimenez-Roqueplo, Anne-Paule
  • Pierre Rustin
Type
Published Article
Journal
American Journal of Physiology-Cell Physiology
Publisher
American Physiological Society
Publication Date
Dec 11, 2006
Volume
291
Issue
6
Identifiers
DOI: 10.1152/ajpcell.00216.2006
PMID: 16760265
Source
USPC - SET - SVS
License
Green

Abstract

A renewed interest in tricarboxylic acid cycle enzymopathies has resulted from the report that, in addition to devastating encephalopathies, these can result in various types of tumors in human. We first review the major features of the cycle that may underlie this surprising variety of clinical features. After discussing the rare cases of encephalopathies associated with specific deficiencies of some of the tricarboxylic acid cycle enzyme, we finally examine the mechanism possibly causing tumor/cancer formation in the cases of mutations affecting fumarase or succinate dehydrogenase genes.

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