MOLECULAR HETEROGENEITY OF THE PML GENE REARRANGEMENT IN ACUTE PROMYELOCYTIC LEUKEMIA - PREVALENCE AND CLINICAL-SIGNIFICANCE

被引:23
作者
FUKUTANI, H
NAOE, T
YOSHIDA, H
YAMAMORI, S
OHNO, R
机构
[1] NAGOYA UNIV,HOSP BRANCH,DEPT INTERNAL MED,1-1-20 DAIKO MINAMI,HIGASHI KU,NAGOYA 461,JAPAN
[2] MITSUBISHI YUKA BIO CLIN LABS INC,ITABASHI KU,TOKYO 174,JAPAN
来源
JAPANESE JOURNAL OF CANCER RESEARCH | 1993年 / 84卷 / 03期
关键词
ACUTE PROMYELOCYTIC LEUKEMIA; GENE REARRANGEMENT; PML; ALL-TRANS-RETINOIC ACID;
D O I
10.1111/j.1349-7006.1993.tb02865.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We determined the breakpoints of the RAR-alpha and PML genes in acute promyelocytic leukemia (APL) cells from 40 patients using Southern blot analysis. We also analyzed the relationship between the location of breakpoints, the clinical features of APL and the response to all-trans retinoic acid (ATRA). While the breakpoints of the RAR-alpha gene were consistently within intron 2, we found two major clusters in the breakpoints of the PML gene. The two breakpoint clusters in the PML gene were separated by 10 kb; 5' breakpoints were in intron 3, and 3' breakpoints were around introns 5 and 6. Twenty percent of the patients had 5' breakpoints in the PML gene and 70% had 3' breakpoints. No rearrangement was observed in the remaining 10% of patients in spite of the presence of t(15;17) translocation. There was no relationship between the location of the PML breakpoints, the clinical features at diagnosis and the response to ATRA.
引用
收藏
页码:257 / 264
页数:8
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