Pathogenesis of polycythaemia vera

被引:25
作者
Hinshelwood, S [1 ]
Bench, AJ [1 ]
Green, AR [1 ]
机构
[1] Univ Cambridge, Ctr Mrc, Dept Haematol, Cambridge CB2 2QH, England
关键词
D O I
10.1016/S0268-960X(97)90021-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Polycythaemia vera (PV) is thought to result from clonal expansion of a transformed multipotent stem cell, Progenitors from patients with PV display abnormal responses to several growth factors, suggesting the presence of a defect in a signalling pathway common to different growth factors, A number of approaches are now focused on defining the molecular lesion or lesions, Identification of causal genes will be of considerable interest both to clinicians, who currently lack a specific and sensitive diagnostic test, and to scientists interested in fundamental issues of stem cell behaviour.
引用
收藏
页码:224 / 232
页数:9
相关论文
共 75 条
  • [1] POLYCYTHEMIA-VERA - FURTHER INVITRO STUDIES OF HEMATOPOIETIC REGULATION
    ADAMSON, JW
    SINGER, JW
    CATALANO, P
    MURPHY, S
    LIN, N
    STEINMANN, L
    ERNST, C
    FIALKOW, PJ
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1980, 66 (06) : 1363 - 1368
  • [2] POLYCYTHEMIA-VERA - STEM-CELL AND PROBABLE CLONAL ORIGIN OF DISEASE
    ADAMSON, JW
    FIALKOW, PJ
    MURPHY, S
    PRCHAL, JF
    STEINMANN, L
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1976, 295 (17) : 913 - 916
  • [3] ANGER B, 1990, LEUKEMIA, V4, P258
  • [4] Asimakopoulos FA, 1996, BRIT J HAEMATOL, V95, P219
  • [5] The gene encoding hematopoietic cell phosphatase (SHP-1) is structurally and transcriptionally intact in polycythemia vera
    Asimakopoulos, FA
    Hinshelwood, S
    Gilbert, JGR
    Delibrias, CC
    Gottgens, B
    Fearon, DT
    Green, AR
    [J]. ONCOGENE, 1997, 14 (10) : 1215 - 1222
  • [6] MOLECULAR ANALYSIS OF CHROMOSOME 20Q DELETIONS ASSOCIATED WITH MYELOPROLIFERATIVE DISORDERS AND MYELODYSPLASTIC SYNDROMES
    ASIMAKOPOULOS, FA
    WHITE, NJ
    NACHEVA, E
    GREEN, AR
    [J]. BLOOD, 1994, 84 (09) : 3086 - 3094
  • [7] Detection of chromosome 20q deletions in bone marrow metaphases but not peripheral blood granulocytes in patients with myeloproliferative disorders or myelodysplastic syndromes
    Asimakopoulos, FA
    Holloway, TL
    Nacheva, EP
    Scott, MA
    Fenaux, P
    Green, AR
    [J]. BLOOD, 1996, 87 (04) : 1561 - 1570
  • [8] Interstitial deletion constitutes the major mechanism for loss of heterozygosity on chromosome 20q in polycythemia vera
    Asimakopoulos, FA
    Gilbert, JGR
    Aldred, MA
    Pearson, TC
    Green, AR
    [J]. BLOOD, 1996, 88 (07) : 2690 - 2698
  • [9] BENCH AJ, UNPUB CONSTRUCTION D
  • [10] Busque L, 1996, BLOOD, V88, P59