Heterogenous expression of bcr-abl fusion mRNA in a patient with Philadelphia-chromosome-positive acute lymphoblastic leukaemia

被引:12
作者
Inokuchi, K
Futaki, M
Hanawa, H
Tanosaki, S
Yamaguchi, H
Iwakiri, R
Nomura, T
Dan, K
机构
[1] Division of Haematology, Third Dept. of Internal Medicine, Nippon Medical School, Tokyo
[2] Nippon Medical School, Tokyo
[3] Division of Haematology, Third Dept. of Internal Medicine, Nippon Medical School, 1-1-5, Sendagi, Bunkyo-ku
关键词
acute lymphoblastic leukaemia; Philadelphia chromosome; bcr-abl gene; RT-PCR; alternative splicing;
D O I
10.1046/j.1365-2141.1997.1452959.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We performed molecular and cytogenetic analysis on a 56-year-old woman with Philadelphia chromosome (Ph-1)-positive acute lymphoblastic leukaemia (ALL) having two types of major and minor bcr-abl (M-bcr-abl, m-bcr-abl) fusion mRNA at diagnosis. In the course of her disease, unexpected heterogenous bcr-abl fusion mRNA was detected by sequential analysis using the reverse transcription and polymerase chain reaction (RT-PCR). The RT-PCR analysis showed both M-bcr-abl (b2-a2 type) and m-bcr-abl at diagnosis, Although b2-a2 type M-bcr-abl disappeared after complete remission (CR) was achieved with intensive induction chemotherapy, expression of both m-bcr-abl and a new type of M-bcr-abl mRNA (bl-a2 type), which may have been produced through splicing out of exon b2, was detected in the early stage of CR. The leukaemic cells contained these heterogenous bcr-abl mRNAs in both the CR and relapsed state, and showed more stable expression of the m-bcr-abl type mRNA than that of the b2-a2 type. These findings of heterogenous bcr-abl mRNA due to alternative or missplicing during the disease course in the present ALL case may provide important evidence of disease progression.
引用
收藏
页码:837 / 840
页数:4
相关论文
共 13 条
[1]  
ABO J, 1993, BLOOD, V82, P2829
[2]   ADDITIONAL C-ABL/BCR REARRANGEMENTS IN A CML PATIENT EXHIBITING 2 PH1-CHROMOSOMES DURING BLAST CRISIS [J].
BARTRAM, CR ;
DEKLEIN, A ;
HAGEMEIJER, A ;
CARBONELL, F ;
KLEIHAUER, E ;
GROSVELD, G .
LEUKEMIA RESEARCH, 1986, 10 (02) :221-225
[3]   PHILADELPHIA-POSITIVE ACUTE-LEUKEMIA - CYTOGENETIC AND MOLECULAR ASPECTS [J].
BERGER, R ;
CHEN, SJ ;
CHEN, Z .
CANCER GENETICS AND CYTOGENETICS, 1990, 44 (02) :143-152
[4]   PH-CHROMOSOME POSITIVE ACUTE LEUKEMIAS AND ACUTE PHASE CML - ONE OR 2 DISEASES - 2 [J].
GALE, RP ;
BUTTURINI, A .
LEUKEMIA RESEARCH, 1990, 14 (04) :295-297
[5]  
HERMANS A, 1988, LEUKEMIA, V2, P628
[6]   UNEXPECTED HETEROGENEITY OF BCR ABL FUSION MESSENGER-RNA DETECTED BY POLYMERASE CHAIN-REACTION IN PHILADELPHIA CHROMOSOME-POSITIVE ACUTE LYMPHOBLASTIC-LEUKEMIA [J].
HOOBERMAN, AL ;
CARRINO, JJ ;
LEIBOWITZ, D ;
ROWLEY, JD ;
LEBEAU, MM ;
ARLIN, ZA ;
WESTBROOK, CA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (11) :4259-4263
[7]   POSSIBLE CORRELATION OF B3-A2-TYPE BCR-ABL MESSENGER-RNA DEFINED BY SEMIQUANTITATIVE RT-PCR TO PLATELET AND MEGAKARYOCYTE COUNTS IN PHILADELPHIA-POSITIVE CHRONIC MYELOGENOUS LEUKEMIA [J].
INOKUCHI, K ;
FUTAKI, M ;
DAN, K ;
NOMURA, T .
INTERNAL MEDICINE, 1994, 33 (04) :189-192
[8]   SIGNIFICANCE OF THE P210 VERSUS P190 MOLECULAR ABNORMALITIES IN ADULTS WITH PHILADELPHIA CHROMOSOME-POSITIVE ACUTE-LEUKEMIA [J].
KANTARJIAN, HM ;
TALPAZ, M ;
DHINGRA, K ;
ESTEY, E ;
KEATING, MJ ;
KU, S ;
TRUJILLO, J ;
HUH, Y ;
STASS, S ;
KURZROCK, R .
BLOOD, 1991, 78 (09) :2411-2418
[9]   DIFFERENCES IN ONCOGENIC POTENCY BUT NOT TARGET-CELL SPECIFICITY DISTINGUISH THE 2 FORMS OF THE BCR/ABL ONCOGENE [J].
KELLIHER, M ;
KNOTT, A ;
MCLAUGHLIN, J ;
WITTE, ON ;
ROSENBERG, N .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (09) :4710-4716
[10]  
KURZROCK R, 1988, NEW ENGL J MED, V319, P990