INDUCTION OF CHRONIC MYELOGENOUS LEUKEMIA IN MICE BY THE P210BCR/ABL GENE OF THE PHILADELPHIA-CHROMOSOME

被引:1862
作者
DALEY, GQ
VANETTEN, RA
BALTIMORE, D
机构
[1] BRIGHAM & WOMENS HOSP, DIV HEMATOL, BOSTON, MA 02115 USA
[2] BRIGHAM & WOMENS HOSP, DEPT MED, BOSTON, MA 02115 USA
[3] MIT, DEPT BIOL, CAMBRIDGE, MA 02142 USA
[4] HARVARD UNIV, SCH MED, BOSTON, MA 02115 USA
关键词
D O I
10.1126/science.2406902
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In tumor cells from virtually all patients with chronic myelogenous leukemia, the Philadelphia chromosome, a fusion of chromosomes 9 and 22, directs the synthesis of the P210bcr/abl protein. The protein-tyrosine kinase activity and hybrid structure of P210bcr/abl are similar to the oncogene product of the Abelson murine leukemia virus, P160 gag/v-abl, which induces acute lymphomas. To determine whether P210bcr/abl can induce chronic myelogenous leukemia, murine bone marrow was infected with a retrovirus encoding P210bcr/abl and transplanted into irradiated syngeneic recipients. Transplant recipients developed several hematologic malignancies; prominent among them was a myeloproliferative syndrome closely resembling the chronic phase of human chronic myelogenous leukemia. Tumor tissue from diseased mice harbored the provirus encoding P210bcr/abl. These results demonstrate that P210bcr/abl expression can induce chronic myelogenous leukemia. Retrovirus-mediated expression of the protein provides a murine model system for further analysis of the disease.
引用
收藏
页码:824 / 830
页数:7
相关论文
共 38 条
[31]   FUSED TRANSCRIPT OF ABL AND BCR GENES IN CHRONIC MYELOGENOUS LEUKEMIA [J].
SHTIVELMAN, E ;
LIFSHITZ, B ;
GALE, RP ;
CANAANI, E .
NATURE, 1985, 315 (6020) :550-554
[32]   PURIFICATION AND CHARACTERIZATION OF MOUSE HEMATOPOIETIC STEM-CELLS [J].
SPANGRUDE, GJ ;
HEIMFELD, S ;
WEISSMAN, IL .
SCIENCE, 1988, 241 (4861) :58-62
[33]   LONG TERMINAL REPEAT SEQUENCES IMPART HEMATOPOIETIC TRANSFORMATION PROPERTIES TO THE MYELOPROLIFERATIVE SARCOMA-VIRUS [J].
STOCKING, C ;
KOLLEK, R ;
BERGHOLZ, U ;
OSTERTAG, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (17) :5746-5750
[34]   IDENTIFICATION OF A NOVEL BONE MARROW-DERIVED B-CELL PROGENITOR POPULATION THAT COEXPRESSES B220 AND THY-1 AND IS HIGHLY ENRICHED FOR ABELSON LEUKEMIA-VIRUS TARGETS [J].
TIDMARSH, GF ;
HEIMFELD, S ;
WHITLOCK, CA ;
WEISSMAN, IL ;
MULLERSIEBURG, CE .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (06) :2665-2671
[35]  
VANETTEN R, UNPUB
[36]   THE MOUSE TYPE-IV C-ABL GENE-PRODUCT IS A NUCLEAR-PROTEIN, AND ACTIVATION OF TRANSFORMING ABILITY IS ASSOCIATED WITH CYTOPLASMIC LOCALIZATION [J].
VANETTEN, RA ;
JACKSON, P ;
BALTIMORE, D .
CELL, 1989, 58 (04) :669-678
[37]   RETROVIRUS-MEDIATED TRANSFER AND EXPRESSION OF THE INTERLEUKIN-3 GENE IN MOUSE HEMATOPOIETIC-CELLS RESULT IN A MYELOPROLIFERATIVE DISORDER [J].
WONG, PMC ;
CHUNG, SW ;
DUNBAR, CE ;
BODINE, DM ;
RUSCETTI, S ;
NIENHUIS, AW .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (02) :798-808
[38]   SELECTIVE TRANSFORMATION OF PRIMITIVE LYMPHOID-CELLS BY THE BCR ABL ONCOGENE EXPRESSED IN LONG-TERM LYMPHOID OR MYELOID CULTURES [J].
YOUNG, JC ;
WITTE, ON .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (10) :4079-4087