THE RECEPTOR TYROSINE KINASE P185(HER2) IS EXPRESSED ON A SUBSET OF B-LYMPHOID BLASTS FROM PATIENTS WITH ACUTE LYMPHOBLASTIC-LEUKEMIA AND CHRONIC MYELOGENOUS LEUKEMIA

被引:39
作者
BUHRING, HJ
SURES, I
JALLAL, B
WEISS, FU
BUSCH, FW
LUDWIG, WD
HANDGRETINGER, R
WALLER, HD
ULLRICH, A
机构
[1] MAX PLANCK INST BIOCHEM,DEPT BIOL MOLEC,MARTINSRIED,GERMANY
[2] ROBERT BOSCH KRANKENHAUS,DEPT HEMATOL,STUTTGART,GERMANY
[3] ROBERT ROSSLE HOSP,DEPT MED ONCOL,BERLIN,GERMANY
[4] UNIV TUBINGEN,CHILDRENS HOSP,TUBINGEN,GERMANY
关键词
D O I
10.1182/blood.V86.5.1916.bloodjournal8651916
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The class I receptor tyrosine kinase (RTK) HER2 is an oncoprotein that is frequently involved in the pathogenesis of tumors of epithelial origin, Here we report mRNA expression in peripheral blood and bone marrow cells from healthy donors in hematopoietic cell lines acid leukemic blasts from patients with acute lymphoblastic leukemia (ALL), acute myeloblastic leukemia (AML), chronic lymphoblastic leukemia (CLL), and chronic myeloid leukemia (CML). However, cell surface expression of HER2 protein (p185(HER2)) was found exclusively on a subset of leukemic cells of the B-lymphoblastic lineage, p185(HER2) expression was found on blasts in 2 of 15 samples from infants, 9 of 19 samples from adult patients with C-ALL (CD19(+)CD10(+)), and 1 of 2 samples from patients with pro-B ALL (CD19(+)CD10(-)), whereas none of the leukemic cells from patients with AML (0/30), T-ALL (0/7), CLL (0/5) (CD19(+)CD5(+)), or CML in chronic and accelerated phase (0/ 5) or in blast crisis with myeloid differentiation (0/14) were positive for p185(HER2). However, cells from 3 of 4 patients with CML in B-lymphoid blast crisis (CD19(+)CD10(+)) expressed high levels of p185(HER2), which was also found on the surface of the CML-derived B-cell lines BV-173 and Nalm-1. Our study shows p185(HER2) expression on malignant cells of hematopoietic origin for the first time. Aberrant expression of this oncogenic receptor tyrosine kinase in hematopoietic cell types may be an oncogenic event contributing to the development of a subset of B-lymphoblastic leukemias. (C) 1995 by The American Society of Hematology.
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页码:1916 / 1923
页数:8
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