PH-POSITIVE LEUKEMIA - A TRANSGENIC MOUSE MODEL

被引:8
|
作者
GROFFEN, J
VONCKEN, JW
KAARTINEN, V
MORRIS, C
HEISTERKAMP, N
机构
[1] Section of Molecular Diagnosis, Department of Pathology, Children's Hospital of Los Angeles, Los Angeles
[2] Cytogenetic and Molecular Oncology Unit, Christchurch Hospital, Christchurch
关键词
LEUKEMIA; BCR/ABL; MOUSE MODEL; TRANSGENIC;
D O I
10.3109/10428199309047857
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The presence of the BCR/ABL chimeric gene is the hallmark of defined types of human leukemia. To increase our knowledge of the oncogenic processes and to develop a model for this type of leukemia we generated a BCR/ABL (P190) transgenic mouse line. Over 95% of mice of this line die of leukemia or leukemia/lymphoma within 35-200 days of age. Karyotypically visible genetic alterations were absent from the early stages of BCR/ABL generated leukemia. A high frequency of aneuploidy was found in advanced leukemia indicating a primary and pivotal role for BCR/ABL in leukemogenesis. Moreover, the data suggest that BCR/ABL has a destabilizing effect on the regulation of the cell cycle. BCR/ABL expression was also found in tissues other than hematopoietic cells. However, this did not result in the development of solid tumors, strongly suggesting that the oncogenicity of BCR/ABL is limited to the hematopoietic lineage.
引用
收藏
页码:19 / 24
页数:6
相关论文
共 50 条
  • [21] Quinacrine Depletes BCR-ABL and Suppresses Ph-Positive Leukemia Cells
    Lei, Hu
    Tu, Yaoyao
    Yang, Li
    Jin, Jin
    Luo, Hao
    Xu, Hanzhang
    Kang, Jingwu
    Zhou, Li
    Wu, Yingli
    CANCER INVESTIGATION, 2019, 37 (06) : 242 - 252
  • [22] INTENSIVE TREATMENT IN ORDER TO MINIMIZE THE PH-POSITIVE CLONE IN CHRONIC MYELOGENIC LEUKEMIA
    SIMONSSON, B
    OBERG, G
    BJOREMAN, M
    BJORKHOLM, M
    GAHRTON, G
    HAST, R
    KILLANDER, A
    TURESSON, I
    UDEN, AM
    VIKROT, O
    VILEN, L
    WAHLIN, A
    CARNESKOG, J
    WESTLIN, J
    LEUKEMIA & LYMPHOMA, 1992, 7 : 55 - 57
  • [23] INTENSIVE TREATMENT IN ORDER TO MINIMIZE THE PH-POSITIVE CLONE IN CHRONIC MYELOGENIC LEUKEMIA
    SIMONSSON, B
    OBERG, G
    KILLANDER, A
    BJOREMAN, M
    BJORKHOLM, M
    GAHRTON, G
    HAST, R
    TURESSON, I
    UDEN, AM
    MALM, C
    VILEN, L
    WAHLIN, A
    LOFVENBERG, E
    CARNESKOG, J
    WESTIN, J
    STEM CELLS, 1993, 11 : 73 - 76
  • [24] EFFICACY OF ALPHA-INTERFERON TREATMENT IN AN UNUSUAL CASE OF PH-POSITIVE LEUKEMIA
    HAAS, OA
    MOR, W
    BARTRAM, C
    AMBROS, P
    GASTL, G
    GADNER, H
    BLUT, 1987, 55 (04): : 295 - 295
  • [25] 2 UNUSUAL COMPLEX TRANSLOCATIONS IN PH-POSITIVE CHRONIC MYELOID-LEUKEMIA
    PINKERTON, PH
    LONDON, B
    COWAN, DH
    SENN, JS
    CANCER GENETICS AND CYTOGENETICS, 1987, 27 (02) : 375 - 377
  • [26] PH-POSITIVE CHRONIC MYELOGENOUS LEUKEMIA EVOLVING AFTER POLYCYTHEMIA-VERA
    JANTUNEN, E
    NOUSIAINEN, T
    AMERICAN JOURNAL OF HEMATOLOGY, 1991, 37 (03) : 212 - 212
  • [27] A cryptic chromosome 19 abnormality in a patient with Ph-positive acute lymphoblastic leukemia
    Berger, R
    Busson, M
    Romana, SP
    CANCER GENETICS AND CYTOGENETICS, 2006, 165 (01) : 79 - 80
  • [28] Strategy of present-day therapy of Ph-positive chronic myeloid leukemia
    Khoroshko, ND
    Turkina, AG
    Zhuravlev, VS
    Sokolova, MA
    Mikhailova, IN
    Zakharova, AV
    Domracheva, EV
    Semenova, EA
    TERAPEVTICHESKII ARKHIV, 1996, 68 (07) : 22 - 27
  • [29] CHEMOTHERAPY FOR PATIENTS IN THE BLASTIC PHASE OF PH-POSITIVE CHRONIC MYELOID-LEUKEMIA
    SADAMORI, N
    ACTA HAEMATOLOGICA JAPONICA, 1990, 53 (08): : 1594 - 1601
  • [30] FURTHER CYTOGENETIC EVIDENCE FOR A MULTISTEP PATHOGENESIS OF PH-POSITIVE CHRONIC MYELOGENOUS LEUKEMIA
    BARBIERI, D
    FERRARESI, P
    CASTOLDI, G
    CANCER GENETICS AND CYTOGENETICS, 1985, 14 (1-2) : 111 - 117