''N-ras gene point mutations in Brazilian acute myelogenous leukemia patients correlate with a poor prognosis''

被引:24
作者
DeMelo, MB
LorandMetze, I
Lima, CSP
Saad, STO
Costa, FF
机构
[1] Department of Clinical Medicine-Hemocentro, School of Medical Sciences, University of Campinas (UNICAMP, Campinas, SP
关键词
oncogene; N-ras; mutations; AML; ACUTE MYELOID-LEUKEMIA; POLYMERASE CHAIN-REACTION; MYELODYSPLASTIC SYNDROMES; CLINICAL-SIGNIFICANCE; ONCOGENE ACTIVATION; COOPERATIVE GROUP; HUMAN-LUNG; AMPLIFICATION; CANCERS; CHEMOTHERAPY;
D O I
10.3109/10428199709039018
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The frequency of ras gene mutations varies from 11 to 27% in AML populations from the United States and Europe but it seems that there is no study regarding the frequency of mutated N-ras gene in patients with AML in South America. In order to study the frequency of N-ras gene mutations (exons 1 and 2) in Brazilian patients with AML and to evaluate the possible correlation between the presence of the mutation and clinical features, 40 patients were analyzed. N-ras mutations were identified in DNA samples from eight of 40 AML patients (20%). No significant correlation was found between N-ras mutation and age, sex, race, response to therapy, FAB subtype or occupational exposure. However, the overall survival and AML-free survival were significantly shorter in patients with N-ras mutations than in those without these abnormalities.
引用
收藏
页码:309 / 317
页数:9
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