A ROLE FOR MITOCHONDRIAL-DNA IN THE PATHOGENESIS OF RADIATION-INDUCED MYELODYSPLASIA AND SECONDARY LEUKEMIA

被引:14
|
作者
HATFILL, SJ
LACOCK, CJR
LAUBSCHER, R
DOWNING, TG
KIRBY, R
机构
[1] UNIV STELLENBOSCH,TYGERBERG HOSP,DEPT VIROL,TYGERBERG 7505,SOUTH AFRICA
[2] RHODES UNIV,DEPT MICROBIOL,GRAHAMSTOWN 6140,SOUTH AFRICA
关键词
MITOCHONDRIA; PRELEUKEMIA; LEUKEMIA; MYELODYSPLASTIC SYNDROMES; MDS;
D O I
10.1016/0145-2126(93)90036-K
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The onset of acute myeloid leukemia following ionizing radiation or alkylating agent exposure is antedated months to years by the development of 'preleukemia', or secondary myelodysplastic syndrome (sMDS). Mitochondrial abnormalities induced by chloramphenicol and clonal deletions of mitochondrial DNA (mt DNA) in the bone marrow create hematological defects similar to sMDS, and abnormal dimers of mt DNA are observed in acute leukemia. This suggests a role for mt DNA in the pathogenesis of sMDS and secondary leukemia. We outline disparate experimental evidence to support this concept and suggest a role for select protease inhibitors in the clinical management of this disorder.
引用
收藏
页码:907 / 913
页数:7
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