Consistent amounts of acute leukemia-associated P190BCR/ABL transcripts are expressed by chronic myelogenous leukemia patients at diagnosis

被引:99
作者
Saglio, G
Pane, F
Gottardi, E
Frigeri, F
Buonaiuto, MR
Guerrasio, A
DeMicheli, D
Parziale, A
Fornaci, MN
Martinelli, G
Salvatore, F
机构
[1] CEINGE,BIOTECNOL AVANZATE,NAPLES,ITALY
[2] UNIV NAPLES FEDERICO II,DIPARTIMENTO BIOCHIM & BIOTECNOL MED,NAPLES,ITALY
[3] UNIV BOLOGNA,IST EMATOL L&A SERAGNOLI,BOLOGNA,ITALY
关键词
D O I
10.1182/blood.V87.3.1075.bloodjournal8731075
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In chronic myelogenous leukemia (CML), the Philadelphia (Ph) chromosome translocation results in the formation of BCR/ABL genes, normally transcribed in two types of hybrid transcripts with a b2a2 or b3a2 BCR/ABL junction, which give origin to 210-kD fusion proteins (P210). A third type of BCR/ABL (with e1a2 type of junction) has been identified in approximately 50% of the Ph-positive acute lymphoblastic leukemia (Ph+ALL) cases and results in the production of a BCR/ABL protein of 190 kD (P190). The presence of this transcript has been associated almost exclusively with the presence of an acute leukemia phenotype. By contrast, here we describe that in addition to transcripts with the b2a2 and b3a2 types of junction corresponding to the P210 proteins, virtually all CMLs at diagnosis bear also BCR/ABL transcripts showing the e1a2 type of junction, which correspond to the acute leukemia-associated P190 protein, With a quantitative polymerase chain reaction assay we found that the amount of the e1a2 mRNA present in CMLs in chronic phase, although in absolute amount much lower than that present in Ph+ALLs, represents in most cases approximately 20% to 30% of the total BCR/ABL transcripts. Moreover, using a novel and very sensitive Western blot technique, we detected relevant amounts of P190 protein in addition to P210 from peripheral cells of two of the patients. (C) 1996 by The American Society of Hematology.
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页码:1075 / 1080
页数:6
相关论文
共 19 条
[1]   UNIQUE FORMS OF THE ABL TYROSINE KINASE DISTINGUISH PH1-POSITIVE CML FROM PH1-POSITIVE ALL [J].
CLARK, SS ;
MCLAUGHLIN, J ;
CRIST, WM ;
CHAMPLIN, R ;
WITTE, ON .
SCIENCE, 1987, 235 (4784) :85-88
[2]  
CROSS NCP, 1993, BLOOD, V82, P1929
[3]  
DHINGRA K, 1991, LEUKEMIA, V5, P191
[4]   PHILADELPHIA CHROMOSOMAL BREAKPOINTS ARE CLUSTERED WITHIN A LIMITED REGION, BCR, ON CHROMOSOME-22 [J].
GROFFEN, J ;
STEPHENSON, JR ;
HEISTERKAMP, N ;
DEKLEIN, A ;
BARTRAM, CR ;
GROSVELD, G .
CELL, 1984, 36 (01) :93-99
[5]  
GUERRASIO A, 1992, LEUKEMIA, V6, P507
[6]   UNIQUE FUSION OF BCR AND C-ABL GENES IN PHILADELPHIA-CHROMOSOME POSITIVE ACUTE LYMPHOBLASTIC-LEUKEMIA [J].
HERMANS, A ;
HEISTERKAMP, N ;
VONLINDERN, M ;
VANBAAL, S ;
MEIJER, D ;
VANDERPLAS, D ;
WIEDEMANN, LM ;
GROFFEN, J ;
BOOTSMA, D ;
GROSVELD, G .
CELL, 1987, 51 (01) :33-40
[7]   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
[8]   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
[9]  
KURZROCK R, 1988, NEW ENGL J MED, V319, P990
[10]  
KUWAO F, 1993, LEUKEMIA, V7, P1168