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Volumn 17, Issue 5, 2003, Pages 1151-1158

Classification and molecular biology of polycythemias (erythrocytoses) and thrombocytosis

Author keywords

[No Author keywords available]

Indexed keywords

2,3 DIPHOSPHOGLYCERIC ACID; CYTOKINE; DIPEPTIDYL CARBOXYPEPTIDASE INHIBITOR; ERYTHROPOIETIN; HEMOGLOBIN; HYPOXIA INDUCIBLE FACTOR 1; LOSARTAN; MESSENGER RNA; VASCULOTROPIN;

EID: 0141730223     PISSN: 08898588     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0889-8588(03)00090-X     Document Type: Review
Times cited : (31)

References (43)
  • 1
    • 0035574894 scopus 로고    scopus 로고
    • Lessons to better understanding of hypoxia sensing: Acquired and congenital mutations resulting in polycythemia
    • Prchal JT, Divoky V. Lessons to better understanding of hypoxia sensing: acquired and congenital mutations resulting in polycythemia. Adv Exp Med Biol 2001;502:189-205.
    • (2001) Adv Exp Med Biol , vol.502 , pp. 189-205
    • Prchal, J.T.1    Divoky, V.2
  • 3
    • 0016793754 scopus 로고
    • Diagnosis and classification of polycythemias
    • Berlin NI. Diagnosis and classification of polycythemias. Semin Hematol 1975;12:339-51.
    • (1975) Semin Hematol , vol.12 , pp. 339-351
    • Berlin, N.I.1
  • 4
    • 0017119808 scopus 로고
    • Human erythroid colony formation in vitro: Evidence for clonal origin
    • Prchal JF, Adamson JW, Steinmann L, Fialkow PJ. Human erythroid colony formation in vitro: evidence for clonal origin. J Cell Physiol 1976;89:489-92.
    • (1976) J Cell Physiol , vol.89 , pp. 489-492
    • Prchal, J.F.1    Adamson, J.W.2    Steinmann, L.3    Fialkow, P.J.4
  • 5
    • 0016391236 scopus 로고
    • Bone-marrow responses in polycythemia vera
    • Prchal JF, Axelrad AA. Bone-marrow responses in polycythemia vera [letter]. N Engl J Med 1974;290:1382.
    • (1974) N Engl J Med , vol.290 , pp. 1382
    • Prchal, J.F.1    Axelrad, A.A.2
  • 6
    • 0028146159 scopus 로고
    • Anti-erythropoietin (EPO) receptor monoclonal antibodies distinguish EPO-dependent and EPO-independent erythroid progenitors in polycythemia vera
    • Fisher MJ, Prchal JF, Prchal JT, D'Andrea AD. Anti-erythropoietin (EPO) receptor monoclonal antibodies distinguish EPO-dependent and EPO-independent erythroid progenitors in polycythemia vera. Blood 1994;84:1982-91.
    • (1994) Blood , vol.84 , pp. 1982-1991
    • Fisher, M.J.1    Prchal, J.F.2    Prchal, J.T.3    D'Andrea, A.D.4
  • 7
    • 2642609475 scopus 로고    scopus 로고
    • Impaired expression of the thrombopoietin receptor by platelets from patients with polycythemia vera
    • Moliterno AR, Hankins WD, Spivak JL. Impaired expression of the thrombopoietin receptor by platelets from patients with polycythemia vera. N Engl J Med 1998;338:572-80.
    • (1998) N Engl J Med , vol.338 , pp. 572-580
    • Moliterno, A.R.1    Hankins, W.D.2    Spivak, J.L.3
  • 9
    • 0036786364 scopus 로고    scopus 로고
    • Biochemical characterization of PRV-1, a novel hematopoietic cell surface receptor, which is overexpressed in polycythemia rubra vera
    • Klippel S, Strunck E, Busse CE, Behringer D, Pahl HL. Biochemical characterization of PRV-1, a novel hematopoietic cell surface receptor, which is overexpressed in polycythemia rubra vera. Blood 2002;100:2441-8.
    • (2002) Blood , vol.100 , pp. 2441-2448
    • Klippel, S.1    Strunck, E.2    Busse, C.E.3    Behringer, D.4    Pahl, H.L.5
  • 11
    • 0035383807 scopus 로고    scopus 로고
    • Increased expression of INK4a/ARF locus in polycythemia vera
    • Dai C, Krantz B. Increased expression of INK4a/ARF locus in polycythemia vera. Blood 2001;97:3424-32.
    • (2001) Blood , vol.97 , pp. 3424-3432
    • Dai, C.1    Krantz, B.2
  • 12
    • 0036191941 scopus 로고    scopus 로고
    • Acquired uniparental disomy of chromosome 9p is a frequent stem cell defect inpolycythemia vera
    • Kralovics R, Guan Y, Prchal JT. Acquired uniparental disomy of chromosome 9p is a frequent stem cell defect inpolycythemia vera. Exp Hematol 2002;30:229-36.
    • (2002) Exp Hematol , vol.30 , pp. 229-236
    • Kralovics, R.1    Guan, Y.2    Prchal, J.T.3
  • 13
    • 0036439588 scopus 로고    scopus 로고
    • Exploring polycythaemia vera with fluorescence in situ hybridization: Additional cryptic 9p is the most frequent abnormality detected
    • Najfeld V, Montella L, Scalise A, Fruchtman S. Exploring polycythaemia vera with fluorescence in situ hybridization: additional cryptic 9p is the most frequent abnormality detected. Br J Haematol 2002;119:558-66.
    • (2002) Br J Haematol , vol.119 , pp. 558-566
    • Najfeld, V.1    Montella, L.2    Scalise, A.3    Fruchtman, S.4
  • 15
    • 0035970090 scopus 로고    scopus 로고
    • Mouse model of congenital polycythemia: Homologous replacement of murine gene by mutant human erythropoietin receptor gene
    • Divoky V, Liu Z, Ryan TM, Prchal JF, Townes TM, Prchal JT. Mouse model of congenital polycythemia: homologous replacement of murine gene by mutant human erythropoietin receptor gene. Proc Natl Acad Sci U S A 2001;98:986-91.
    • (2001) Proc Natl Acad Sci U S A , vol.98 , pp. 986-991
    • Divoky, V.1    Liu, Z.2    Ryan, T.M.3    Prchal, J.F.4    Townes, T.M.5    Prchal, J.T.6
  • 16
    • 0034839931 scopus 로고    scopus 로고
    • Genetic heterogeneity of primary familial and congenital polycythemia
    • Kralovics R, Prchal JT. Genetic heterogeneity of primary familial and congenital polycythemia. Am J Hematol 2001;68:115-21.
    • (2001) Am J Hematol , vol.68 , pp. 115-121
    • Kralovics, R.1    Prchal, J.T.2
  • 17
    • 0003023429 scopus 로고    scopus 로고
    • Cytochrome b5 reductase deficiency and enzymopenic hereditary methemoglobinemia
    • Scriver C, Beaudet A, Sly W, Valle D, editors. New York: McGraw-Hill
    • Weatherall DJ, Clegg JB, Higgs DR, Wood WG. Cytochrome b5 reductase deficiency and enzymopenic hereditary methemoglobinemia. In: Scriver C, Beaudet A, Sly W, Valle D, editors. The metabolic and molecular basis of inherited disease. 8th edition. New York: McGraw-Hill; 2001. p. 4571-636.
    • (2001) The Metabolic and Molecular Basis of Inherited Disease. 8th Edition , pp. 4571-4636
    • Weatherall, D.J.1    Clegg, J.B.2    Higgs, D.R.3    Wood, W.G.4
  • 18
    • 0017144203 scopus 로고
    • Detection of mutant hemoglobins with altered affinity for oxygen: A simplified technique
    • Lichtman MA, Murphy MS, Adamson JW. Detection of mutant hemoglobins with altered affinity for oxygen: a simplified technique. Ann Intern Med 1976;84:517-20.
    • (1976) Ann Intern Med , vol.84 , pp. 517-520
    • Lichtman, M.A.1    Murphy, M.S.2    Adamson, J.W.3
  • 20
    • 0005746215 scopus 로고    scopus 로고
    • Red cell enzymopathies
    • Hoffman R, editor. Philadelphia: WB Saunders
    • Prchal JT, Gregg X. Red cell enzymopathies. In: Hoffman R, editor. Hematology. 3rd edition. Philadelphia: WB Saunders; 1999. p. 561-76.
    • (1999) Hematology. 3rd Edition , pp. 561-576
    • Prchal, J.T.1    Gregg, X.2
  • 21
    • 0034663989 scopus 로고    scopus 로고
    • HIF-1 and human disease: One highly involved factor
    • Semenza GL. HIF-1 and human disease: one highly involved factor. Genes Dev 2000;14:1983-91.
    • (2000) Genes Dev , vol.14 , pp. 1983-1991
    • Semenza, G.L.1
  • 22
    • 0033587146 scopus 로고    scopus 로고
    • The tumour suppressor protein VHL targets hypoxia-inducible factors for oxygen-dependent proteolysis
    • Maxwell PH, Wiesener MS, Chang GW, et al. The tumour suppressor protein VHL targets hypoxia-inducible factors for oxygen-dependent proteolysis. Nature 1999;399:271-5.
    • (1999) Nature , vol.399 , pp. 271-275
    • Maxwell, P.H.1    Wiesener, M.S.2    Chang, G.W.3
  • 23
    • 0033407456 scopus 로고    scopus 로고
    • Von Hippel-Lindau syndrome: A pleomorphic condition
    • Friedrich CA. Von Hippel-Lindau syndrome: a pleomorphic condition. Cancer 1999;86:2478-82.
    • (1999) Cancer , vol.86 , pp. 2478-2482
    • Friedrich, C.A.1
  • 24
    • 0016118725 scopus 로고
    • Familial erythrocytosis among the residents of the Chuvash ASSR
    • Poliakova LA. Familial erythrocytosis among the residents of the Chuvash ASSR. Probl Gematol Pereliv Krovi 1974;19:30-3.
    • (1974) Probl Gematol Pereliv Krovi , vol.19 , pp. 30-33
    • Poliakova, L.A.1
  • 26
    • 0036111623 scopus 로고    scopus 로고
    • Endemic polycythemia in Russia: Mutation in the VHL gene
    • Ang SO, Chen H, Gordeuk VR, et al. Endemic polycythemia in Russia: mutation in the VHL gene. Blood Cells Mol Dis 2002;28:57-62.
    • (2002) Blood Cells Mol Dis , vol.28 , pp. 57-62
    • Ang, S.O.1    Chen, H.2    Gordeuk, V.R.3
  • 27
    • 18744373593 scopus 로고    scopus 로고
    • Congenital Chuvash polycythemia: Altered oxygen homeostasis due to homozygosity for a hypomorphic VHL allele
    • Ang SO, Chen H, Hirota K, et al. Congenital Chuvash polycythemia: altered oxygen homeostasis due to homozygosity for a hypomorphic VHL allele. Nat Genet 2002;32:614-21.
    • (2002) Nat Genet , vol.32 , pp. 614-621
    • Ang, S.O.1    Chen, H.2    Hirota, K.3
  • 29
    • 0037441601 scopus 로고    scopus 로고
    • Mutations in the VHL gene in sporadic apparently congenital polycythemia
    • Pastore YD, Jelinek J, Ang S, et al. Mutations in the VHL gene in sporadic apparently congenital polycythemia. Blood 2003;101:1591-5.
    • (2003) Blood , vol.101 , pp. 1591-1595
    • Pastore, Y.D.1    Jelinek, J.2    Ang, S.3
  • 30
    • 0042744741 scopus 로고    scopus 로고
    • Chuvash-type congenital polycythemia in 4 families of Asian and Western European ancestry
    • in press
    • Percy MJ, McMullin MF, Jowitt SN, Potter M, Treacy M, Watson WH, et al. Chuvash-type congenital polycythemia in 4 families of Asian and Western European ancestry. Blood 2003; in press.
    • (2003) Blood
    • Percy, M.J.1    McMullin, M.F.2    Jowitt, S.N.3    Potter, M.4    Treacy, M.5    Watson, W.H.6
  • 32
    • 0031778819 scopus 로고    scopus 로고
    • Losartan, an angiotensin II type 1 receptor antagonist, lowers hematocrit in posttransplant erythrocytosis
    • Julian BA, Brantley Jr RR, Barker CV, et al. Losartan, an angiotensin II type 1 receptor antagonist, lowers hematocrit in posttransplant erythrocytosis. J Am Soc Nephrol 1998;9:1104-8.
    • (1998) J Am Soc Nephrol , vol.9 , pp. 1104-1108
    • Julian, B.A.1    Brantley R.R., Jr.2    Barker, C.V.3
  • 33
    • 0000191789 scopus 로고    scopus 로고
    • Angiotensin II facilitates erythropoietin mediated proliferation of normal early erythroid progenitors
    • Mrug M, Stopka T, Julian BA, Prchal JF, Prchal JT. Angiotensin II facilitates erythropoietin mediated proliferation of normal early erythroid progenitors. J Clin Invest 1997;115:508-22.
    • (1997) J Clin Invest , vol.115 , pp. 508-522
    • Mrug, M.1    Stopka, T.2    Julian, B.A.3    Prchal, J.F.4    Prchal, J.T.5
  • 34
    • 0028278002 scopus 로고
    • Clinical evaluation of erythrocytosis in patients with hepatocellular carcinoma
    • Hwang SJ, Lee SD, Wu JC, et al. Clinical evaluation of erythrocytosis in patients with hepatocellular carcinoma. Chung Hua I Hsueh Tsa Chih 1994;53:262-9.
    • (1994) Chung Hua I Hsueh Tsa Chih , vol.53 , pp. 262-269
    • Hwang, S.J.1    Lee, S.D.2    Wu, J.C.3
  • 35
    • 0035735611 scopus 로고    scopus 로고
    • Thrombocytosis and thrombocythemia
    • Schafer AI. Thrombocytosis and thrombocythemia. Blood Rev 2001;15:159-66.
    • (2001) Blood Rev , vol.15 , pp. 159-166
    • Schafer, A.I.1
  • 36
    • 0028350733 scopus 로고
    • Occurrence, etiology, and clinical significance of extreme thrombocytosis: A study of 280 cases
    • Buss DH, Cashell QAW, Connor ML, Richards F. Occurrence, etiology, and clinical significance of extreme thrombocytosis: a study of 280 cases. Am J Med 1994;96:247-53.
    • (1994) Am J Med , vol.96 , pp. 247-253
    • Buss, D.H.1    Cashell, Q.A.W.2    Connor, M.L.3    Richards, F.4
  • 37
    • 0032322969 scopus 로고    scopus 로고
    • Clonality markers in polycythaemia and primary thrombocythaemia
    • Briere J, el-Kassar N. Clonality markers in polycythaemia and primary thrombocythaemia. Baillieres Clin Haematol 1998;11:787-801.
    • (1998) Baillieres Clin Haematol , vol.11 , pp. 787-801
    • Briere, J.1    El-Kassar, N.2
  • 38
    • 0033555392 scopus 로고    scopus 로고
    • A large proportion of patients with a diagnosis of essential thrombocythemia do not have a clonal disorder and may be at lower risk of thrombotic complications
    • Harrison CN, Gale RE, Machin SJ, Linch DC. A large proportion of patients with a diagnosis of essential thrombocythemia do not have a clonal disorder and may be at lower risk of thrombotic complications. Blood 1999;93:417-24.
    • (1999) Blood , vol.93 , pp. 417-424
    • Harrison, C.N.1    Gale, R.E.2    Machin, S.J.3    Linch, D.C.4
  • 39
    • 0034669997 scopus 로고    scopus 로고
    • Hypersensitivity of circulating progenitor cells to megakaryocyte growth and development factor (PEG-rHu MGDF) in essential thrombocythemia
    • Axelrad AA, Eskinazi D, Correa PN, Amato D. Hypersensitivity of circulating progenitor cells to megakaryocyte growth and development factor (PEG-rHu MGDF) in essential thrombocythemia. Blood 2000;96:3310-21.
    • (2000) Blood , vol.96 , pp. 3310-3321
    • Axelrad, A.A.1    Eskinazi, D.2    Correa, P.N.3    Amato, D.4
  • 40
    • 0031975482 scopus 로고    scopus 로고
    • An activating splice donor mutation in the thrombopoietin gene causes hereditary thrombocythaemia
    • Wiestner A, Schlemper RJ, van der Maas AP, Skoda RC. An activating splice donor mutation in the thrombopoietin gene causes hereditary thrombocythaemia. Nat Genet 1998;18:49-52.
    • (1998) Nat Genet , vol.18 , pp. 49-52
    • Wiestner, A.1    Schlemper, R.J.2    Van der Maas, A.P.3    Skoda, R.C.4
  • 41
    • 0035704766 scopus 로고    scopus 로고
    • Lack of pathogenic mutations in the 5′-untranslated region of the thrombopoietin gene in patients with non-familial essential thrombocythaemia
    • Allen AJ, Gale RE, Harrison CN, Machin SJ, Linch DC. Lack of pathogenic mutations in the 5′-untranslated region of the thrombopoietin gene in patients with non-familial essential thrombocythaemia. Eur J Haematol 2001;67:232-7.
    • (2001) Eur J Haematol , vol.67 , pp. 232-237
    • Allen, A.J.1    Gale, R.E.2    Harrison, C.N.3    Machin, S.J.4    Linch, D.C.5
  • 42
    • 0033897370 scopus 로고    scopus 로고
    • Hereditary thrombocythaemia is a genetically heterogeneous disorder: Exclusion of TPO and MPL in two families with hereditary thrombocythaemia
    • Wiestner A, Padosch SA, Ghilardi N, Cesar JM, Odriozola J, Shapiro A, Skoda RC. Hereditary thrombocythaemia is a genetically heterogeneous disorder: exclusion of TPO and MPL in two families with hereditary thrombocythaemia. Br J Haematol 2000;110:104-9.
    • (2000) Br J Haematol , vol.110 , pp. 104-109
    • Wiestner, A.1    Padosch, S.A.2    Ghilardi, N.3    Cesar, J.M.4    Odriozola, J.5    Shapiro, A.6    Skoda, R.C.7


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