P53 IN CHRONIC MYELOGENOUS LEUKEMIA IN ACUTE PHASE

被引:212
作者
FEINSTEIN, E
CIMINO, G
GALE, RP
ALIMENA, G
BERTHIER, R
KISHI, K
GOLDMAN, J
ZACCARIA, A
BERREBI, A
CANAANI, E
机构
[1] WEIZMANN INST SCI,DEPT CHEM IMMUNOL,IL-76100 REHOVOT,ISRAEL
[2] UNIV CALIF LOS ANGELES,MED CTR,DEPT MED,LOS ANGELES,CA 90024
[3] LA SPAIENZA UNIV,HEMATOL DEPT HUMAN BIOPATHOL,I-00161 ROME,ITALY
[4] CEN,INSERM,U217,F-38041 GRENOBLE,FRANCE
[5] NIIGATA UNIV,DEPT INTERNAL MED,NIIGATA 951,JAPAN
[6] ROYAL POST GRAD SCH,LEUKEMIA UNIT,LONDON W12 OHS,ENGLAND
[7] UNIV BOLOGNA,INST HEMATOL,I-40138 BOLOGNA,ITALY
[8] KAPLAN HOSP,HEMATOL SECT,IL-76100 REHOVOT,ISRAEL
关键词
BLAST CRISIS; SUPPRESSOR GENES; ALLELE LOSS;
D O I
10.1073/pnas.88.14.6293
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
All patients with chronic myelogenous leukemia (CML) undergo clinical transition from chronic to acute phase. This transition is often associated with deletion of the short arm of chromosome 17 in the form of the i(17q) aberration. Since the p53 gene is a suppressor gene and is located on 17p13, we examined the possibility that it is inactivated during progression of CML. Therefore, we studied the structure and expression of p53 in the leukemic cells of a large number of CML patients in acute phase. We found that although the gene is rarely rearranged, one p53 allele is completely deleted in patients with the i(17q) aberration as well as in some patients who do not show karyotypic changes. In all of these patients the remaining allele is inactivated through loss of expression, rearrangement, or point mutation. Detailed analysis of some patients who carry both p53 alleles indicated neither loss of expression nor structural alterations. It appears that p53 loss of function is associated with progression of around 25% of CML patients.
引用
收藏
页码:6293 / 6297
页数:5
相关论文
共 39 条
  • [31] NEW CONSISTENT CHROMOSOMAL ABNORMALITY IN CHRONIC MYELOGENOUS LEUKEMIA IDENTIFIED BY QUINACRINE FLUORESCENCE AND GIEMSA STAINING
    ROWLEY, JD
    [J]. NATURE, 1973, 243 (5405) : 290 - 293
  • [32] CHROMOSOME-ABNORMALITIES IN MALIGNANT HEMATOLOGIC DISEASES
    ROWLEY, JD
    TESTA, JR
    [J]. ADVANCES IN CANCER RESEARCH, 1982, 36 : 103 - 148
  • [33] SHTIVELMAN E, 1987, BLOOD, V69, P971
  • [34] FUSED TRANSCRIPT OF ABL AND BCR GENES IN CHRONIC MYELOGENOUS LEUKEMIA
    SHTIVELMAN, E
    LIFSHITZ, B
    GALE, RP
    CANAANI, E
    [J]. NATURE, 1985, 315 (6020) : 550 - 554
  • [35] FORMATION OF A STABLE TRIPLEX FROM A SINGLE DNA STRAND
    SKLENAR, V
    FEIGON, J
    [J]. NATURE, 1990, 345 (6278) : 836 - 838
  • [36] SOUSSI T, 1990, ONCOGENE, V5, P945
  • [37] P53 - A FREQUENT TARGET FOR GENETIC ABNORMALITIES IN LUNG-CANCER
    TAKAHASHI, T
    NAU, MM
    CHIBA, I
    BIRRER, MJ
    ROSENBERG, RK
    VINOCOUR, M
    LEVITT, M
    PASS, H
    GAZDAR, AF
    MINNA, JD
    [J]. SCIENCE, 1989, 246 (4929) : 491 - 494
  • [38] IMMUNOPHENOTYPE OF BLAST CELLS IN CHRONIC MYELOID-LEUKEMIA
    VALIRON, O
    CLEMANCEYMARCILLE, G
    TROESCH, A
    SCHWEITZER, A
    PRENANT, M
    HOLLARD, D
    BERTHIER, R
    [J]. LEUKEMIA RESEARCH, 1988, 12 (10) : 861 - +
  • [39] ZAKUTHOURI R, 1985, EMBO J, V4, P1751