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Journal of Experimental Hematology ; (6): 712-716, 2008.
Artigo em Chinês | WPRIM | ID: wpr-267905

RESUMO

Mitochondria is the main place of biological oxidation and energy transform. Mitochondrial DNA encodes the complex of respiratory chain in mitochondria and its mutation can cause a series of human disease. Mitochondrial DNA mutation which observed in myelodysplastic syndrome (MDS) patients cause the MDS by the mechanism of iron metabolism disorder, gene instability and hemopoietic progenitor cell apoptosis. In this review the characteristics of mitochondrial DNA structure, the mitochondrial DNA mutation and the possible mechanism of mitochondrial DNA mutation in pathogenesis of MDS were summarized.


Assuntos
Humanos , Anemia Sideroblástica , Genética , DNA Mitocondrial , Genética , Síndromes Mielodisplásicas , Genética , Mutação Puntual
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