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Volumn 93, Issue 5, 2008, Pages 646-648

Molecular basis of thrombocytosis

Author keywords

[No Author keywords available]

Indexed keywords

JANUS KINASE 2; THROMBOPOIETIN;

EID: 43449115112     PISSN: 03906078     EISSN: None     Source Type: Journal    
DOI: 10.3324/haematol.13194     Document Type: Editorial
Times cited : (12)

References (36)
  • 1
    • 38949153807 scopus 로고    scopus 로고
    • Historical review: Megakaryopoiesis and thrombopoiesis
    • Kaushansky K. Historical review: megakaryopoiesis and thrombopoiesis. Blood 2008;111:981-6.
    • (2008) Blood , vol.111 , pp. 981-986
    • Kaushansky, K.1
  • 2
    • 31044443970 scopus 로고    scopus 로고
    • The biogenesis of platelets from megakaryocyte proplatelets
    • Patel SR, Hartwig JH, Italiano JE, Jr. The biogenesis of platelets from megakaryocyte proplatelets. J Clin Invest 2005;115:3348-54.
    • (2005) J Clin Invest , vol.115 , pp. 3348-3354
    • Patel, S.R.1    Hartwig, J.H.2    Italiano Jr., J.E.3
  • 3
    • 0023906446 scopus 로고
    • Human megakaryocytopoiesis: In vitro regulation and characterization of megakaryocytic precursor cells by differentiation markers
    • Vainchenker W, Kieffer N. Human megakaryocytopoiesis: in vitro regulation and characterization of megakaryocytic precursor cells by differentiation markers. Blood Rev 1988; 2:102-7.
    • (1988) Blood Rev , vol.2 , pp. 102-107
    • Vainchenker, W.1    Kieffer, N.2
  • 4
    • 34147179036 scopus 로고    scopus 로고
    • Interrelation between polyploidization and megakaryocyte differentiation: A gene profiling approach
    • Raslova H, Kauffmann A, Sekkai D, Ripoche H, Larbret F, Robert T, et al. Interrelation between polyploidization and megakaryocyte differentiation: a gene profiling approach. Blood 2007;109:3225-34.
    • (2007) Blood , vol.109 , pp. 3225-3234
    • Raslova, H.1    Kauffmann, A.2    Sekkai, D.3    Ripoche, H.4    Larbret, F.5    Robert, T.6
  • 5
    • 0028909690 scopus 로고
    • Thrombopoietin (c-mpl ligand) acts synergistically with erythropoietin, stem cell factor, and interleukin-11 to enhance murine megakaryocyte colony growth and increases megakaryocyte ploidy in vitro
    • Broudy VC, Lin NL, Kaushansky K. Thrombopoietin (c-mpl ligand) acts synergistically with erythropoietin, stem cell factor, and interleukin-11 to enhance murine megakaryocyte colony growth and increases megakaryocyte ploidy in vitro. Blood 1995;85:1719-26.
    • (1995) Blood , vol.85 , pp. 1719-1726
    • Broudy, V.C.1    Lin, N.L.2    Kaushansky, K.3
  • 6
    • 11144356721 scopus 로고    scopus 로고
    • Chemokine-mediated interaction of hematopoietic progenitors with the bone marrow vascular niche is required for thrombopoiesis
    • Avecilla ST, Hattori K, Heissig B, Tejada R, Liao F, Shido K, et al. Chemokine-mediated interaction of hematopoietic progenitors with the bone marrow vascular niche is required for thrombopoiesis. Nat Med 2004;10:64-71.
    • (2004) Nat Med , vol.10 , pp. 64-71
    • Avecilla, S.T.1    Hattori, K.2    Heissig, B.3    Tejada, R.4    Liao, F.5    Shido, K.6
  • 8
    • 0032400867 scopus 로고    scopus 로고
    • Thrombopoietin production is inhibited by a translational mechanism
    • Ghilardi N, Wiestner A, Skoda RC. Thrombopoietin production is inhibited by a translational mechanism. Blood 1998;92:4023-30.
    • (1998) Blood , vol.92 , pp. 4023-4030
    • Ghilardi, N.1    Wiestner, A.2    Skoda, R.C.3
  • 9
    • 1542615163 scopus 로고    scopus 로고
    • Thrombocytosis
    • Schafer AI. Thrombocytosis. N Engl J Med 2004;350:1211-9.
    • (2004) N Engl J Med , vol.350 , pp. 1211-1219
    • Schafer, A.I.1
  • 10
    • 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
  • 11
    • 0032529663 scopus 로고    scopus 로고
    • Familial essential thrombocythemia associated with one-base deletion in the 5′-untranslated region of the thrombopoietin gene
    • Kondo T, Okabe M, Sanada M, Kurosawa M, Suzuki S, Kobayashi M, et al. Familial essential thrombocythemia associated with one-base deletion in the 5′-untranslated region of the thrombopoietin gene. Blood 1998;92:1091-6.
    • (1998) Blood , vol.92 , pp. 1091-1096
    • Kondo, T.1    Okabe, M.2    Sanada, M.3    Kurosawa, M.4    Suzuki, S.5    Kobayashi, M.6
  • 12
    • 0032757997 scopus 로고    scopus 로고
    • Hereditary thrombocythaemia in a Japanese family is caused by a novel point mutation in the thrombopoietin gene
    • Ghilardi N, Wiestner A, Kikuchi M, Ohsaka A, Skoda RC. Hereditary thrombocythaemia in a Japanese family is caused by a novel point mutation in the thrombopoietin gene. Br J Haematol 1999;107:310-6.
    • (1999) Br J Haematol , vol.107 , pp. 310-316
    • Ghilardi, N.1    Wiestner, A.2    Kikuchi, M.3    Ohsaka, A.4    Skoda, R.C.5
  • 13
    • 0033566796 scopus 로고    scopus 로고
    • A single-base deletion in the thrombopoietin (TPO) gene causes familial essential thrombocythemia through a mechanism of more efficient translation of TPO mRNA
    • Ghilardi N, Skoda RC. A single-base deletion in the thrombopoietin (TPO) gene causes familial essential thrombocythemia through a mechanism of more efficient translation of TPO mRNA. Blood 1999;94:1480-2.
    • (1999) Blood , vol.94 , pp. 1480-1482
    • Ghilardi, N.1    Skoda, R.C.2
  • 14
    • 43449085540 scopus 로고    scopus 로고
    • A de novo splice donor mutation in the thrombopoietin gene causes hereditary thrombocythemia in a Polish family
    • Liu K, Kralovics R, Rudzki Z, Grabowska B, Buser AS, Olcaydu D, et al. A de novo splice donor mutation in the thrombopoietin gene causes hereditary thrombocythemia in a Polish family. Haematologica 2008;93:706-14.
    • (2008) Haematologica , vol.93 , pp. 706-714
    • Liu, K.1    Kralovics, R.2    Rudzki, Z.3    Grabowska, B.4    Buser, A.S.5    Olcaydu, D.6
  • 15
    • 2542502506 scopus 로고    scopus 로고
    • Familial essential thrombocythemia associated with a dominant-positive activating mutation of the c-MPL gene, which encodes for the receptor for thrombopoietin
    • Ding J, Komatsu H, Wakita A, Kato-Uranishi M, Ito M, Satoh A, et al. Familial essential thrombocythemia associated with a dominant-positive activating mutation of the c-MPL gene, which encodes for the receptor for thrombopoietin. Blood 2004;103:4198-200.
    • (2004) Blood , vol.103 , pp. 4198-4200
    • Ding, J.1    Komatsu, H.2    Wakita, A.3    Kato-Uranishi, M.4    Ito, M.5    Satoh, A.6
  • 16
    • 34047236618 scopus 로고    scopus 로고
    • Markers of myeloproliferative diseases in childhood polycythemia vera and essential thrombocythemia
    • Teofili L, Giona F, Martini M, Cenci T, Guidi F, Torti L, et al. Markers of myeloproliferative diseases in childhood polycythemia vera and essential thrombocythemia. J Clin Oncol 2007;25:1048-53.
    • (2007) J Clin Oncol , vol.25 , pp. 1048-1053
    • Teofili, L.1    Giona, F.2    Martini, M.3    Cenci, T.4    Guidi, F.5    Torti, L.6
  • 18
    • 28244442441 scopus 로고    scopus 로고
    • Definition of subtypes of essential thrombocythaemia and relation to polycythaemia vera based on JAK2 V617F mutation status: A prospective study
    • Campbell PJ, Scott LM, Buck G, Wheatley K, East CL, Marsden JT, et al. Definition of subtypes of essential thrombocythaemia and relation to polycythaemia vera based on JAK2 V617F mutation status: a prospective study. Lancet 2005;366:1945-53.
    • (2005) Lancet , vol.366 , pp. 1945-1953
    • Campbell, P.J.1    Scott, L.M.2    Buck, G.3    Wheatley, K.4    East, C.L.5    Marsden, J.T.6
  • 19
    • 33746437130 scopus 로고    scopus 로고
    • MPLW515L is a novel somatic activating mutation in myelofibrosis with myeloid metaplasia
    • Pikman Y, Lee BH, Mercher T, McDowell E, Ebert BL, Gozo M, et al. MPLW515L is a novel somatic activating mutation in myelofibrosis with myeloid metaplasia. PLoS Med 2006;3:e270.
    • (2006) PLoS Med , vol.3
    • Pikman, Y.1    Lee, B.H.2    Mercher, T.3    McDowell, E.4    Ebert, B.L.5    Gozo, M.6
  • 20
    • 33750534561 scopus 로고    scopus 로고
    • MPL515 mutations in myeloproliferative and other myeloid disorders: A study of 1182 patients
    • Pardanani AD, Levine RL, Lasho T, Pikman Y, Mesa RA, Wadleigh M, et al. MPL515 mutations in myeloproliferative and other myeloid disorders: a study of 1182 patients. Blood 2006;108:3472-6.
    • (2006) Blood , vol.108 , pp. 3472-3476
    • Pardanani, A.D.1    Levine, R.L.2    Lasho, T.3    Pikman, Y.4    Mesa, R.A.5    Wadleigh, M.6
  • 21
    • 39749133771 scopus 로고    scopus 로고
    • Clinical significance of MPL mutations in essential thrombocythemia: Analysis of the PT-1 cohort [abstract]
    • Beer P, Campbell P, Erber W, Scott L, Bench A, Bareford D, et al. Clinical significance of MPL mutations in essential thrombocythemia: analysis of the PT-1 cohort [abstract]. Blood 2007;110:677.
    • (2007) Blood , vol.110 , pp. 677
    • Beer, P.1    Campbell, P.2    Erber, W.3    Scott, L.4    Bench, A.5    Bareford, D.6
  • 22
    • 43449087815 scopus 로고    scopus 로고
    • Relation between proportion of granulocyte JAK2 (V617F) mutant alleles, clinical phenotype and disease progression in chronic myeloproliferative disorders [abstract]
    • Passamonti F, Rumi E, Pietra D, Elena C, Della Porta M, Arcaini L, et al. Relation between proportion of granulocyte JAK2 (V617F) mutant alleles, clinical phenotype and disease progression in chronic myeloproliferative disorders [abstract]. Haematologica 2006;91 (suppl 1):350.
    • (2006) Haematologica , vol.91 , Issue.SUPPL. 1 , pp. 350
    • Passamonti, F.1    Rumi, E.2    Pietra, D.3    Elena, C.4    Della Porta, M.5    Arcaini, L.6
  • 23
    • 37049036160 scopus 로고    scopus 로고
    • Somatic mutations of JAK2 exon 12 as a molecular basis of erythrocytosis
    • Cazzola M. Somatic mutations of JAK2 exon 12 as a molecular basis of erythrocytosis. Haematologica 2007;92:1585-9.
    • (2007) Haematologica , vol.92 , pp. 1585-1589
    • Cazzola, M.1
  • 25
    • 38549087966 scopus 로고    scopus 로고
    • Myelodysplastic/myeloproliferative disorders
    • Malcovati L, Cazzola M. Myelodysplastic/myeloproliferative disorders. Haematologica 2008;93:4-6.
    • (2008) Haematologica , vol.93 , pp. 4-6
    • Malcovati, L.1    Cazzola, M.2
  • 26
    • 33744478891 scopus 로고    scopus 로고
    • Occurrence of the JAK2 V617F mutation in the WHO provisional entity: Myelodysplastic/myeloproliferative disease, unclassifiable-refractory anemia with ringed sideroblasts associated with marked thrombocytosis
    • Remacha AF, Nomdedeu JF, Puget G, Estivill C, Sarda MP, Canals C, et al. Occurrence of the JAK2 V617F mutation in the WHO provisional entity: myelodysplastic/myeloproliferative disease, unclassifiable-refractory anemia with ringed sideroblasts associated with marked thrombocytosis. Haematologica 2006;91:719-20.
    • (2006) Haematologica , vol.91 , pp. 719-720
    • Remacha, A.F.1    Nomdedeu, J.F.2    Puget, G.3    Estivill, C.4    Sarda, M.P.5    Canals, C.6
  • 27
    • 37749011577 scopus 로고    scopus 로고
    • MPL W515 and JAK2 V617 mutation analysis in patients with refractory anemia with ringed sideroblasts and an elevated platelet count
    • Steensma DP, Caudill JS, Pardanani A, McClure RF, Lasho TL, Tefferi A. MPL W515 and JAK2 V617 mutation analysis in patients with refractory anemia with ringed sideroblasts and an elevated platelet count. Haematologica 2006;91:ECR57.
    • (2006) Haematologica , vol.91
    • Steensma, D.P.1    Caudill, J.S.2    Pardanani, A.3    McClure, R.F.4    Lasho, T.L.5    Tefferi, A.6
  • 28
    • 38549176801 scopus 로고    scopus 로고
    • JAK2V617F mutation status identifies subtypes of refractory anemia with ringed sideroblasts associated with marked thrombocytosis
    • Schmitt-Graeff AH, Teo SS, Olschewski M, Schaub F, Haxelmans S, Kirn A, et al. JAK2V617F mutation status identifies subtypes of refractory anemia with ringed sideroblasts associated with marked thrombocytosis. Haematologica 2008;93:34-40.
    • (2008) Haematologica , vol.93 , pp. 34-40
    • Schmitt-Graeff, A.H.1    Teo, S.S.2    Olschewski, M.3    Schaub, F.4    Haxelmans, S.5    Kirn, A.6
  • 30
    • 0033039333 scopus 로고    scopus 로고
    • Aetiology and clinical significance of thrombocytosis: Analysis of 732 patients with an elevated platelet count
    • Griesshammer M, Bangerter M, Sauer T, Wennauer R, Bergmann L, Heimpel H. Aetiology and clinical significance of thrombocytosis: analysis of 732 patients with an elevated platelet count. J Intern Med 1999;245:295-300.
    • (1999) J Intern Med , vol.245 , pp. 295-300
    • Griesshammer, M.1    Bangerter, M.2    Sauer, T.3    Wennauer, R.4    Bergmann, L.5    Heimpel, H.6
  • 31
    • 0034210637 scopus 로고    scopus 로고
    • Translational pathophysiology: A novel molecular mechanism of human disease
    • Cazzola M, Skoda RC. Translational pathophysiology: a novel molecular mechanism of human disease. Blood 2000;95:3280-8.
    • (2000) Blood , vol.95 , pp. 3280-3288
    • Cazzola, M.1    Skoda, R.C.2
  • 32
    • 33644501833 scopus 로고    scopus 로고
    • Increased platelet and leukocyte activation as contributing mechanisms for thrombosis in essential thrombocythemia and correlation with the JAK2 mutational status
    • Arellano-Rodrigo E, Alvarez-Larran A, Reverter JC, Villamor N, Colomer D, Cervantes F. Increased platelet and leukocyte activation as contributing mechanisms for thrombosis in essential thrombocythemia and correlation with the JAK2 mutational status. Haematologica 2006; 91:169-75.
    • (2006) Haematologica , vol.91 , pp. 169-175
    • Arellano-Rodrigo, E.1    Alvarez-Larran, A.2    Reverter, J.C.3    Villamor, N.4    Colomer, D.5    Cervantes, F.6
  • 33
    • 0031668547 scopus 로고    scopus 로고
    • The activating splice mutation in intron 3 of the thrombopoietin gene is not found in patients with nonfamilial essential thrombocythaemia
    • Harrison CN, Gale RE, Wiestner AC, Skoda RC, Linch DC. The activating splice mutation in intron 3 of the thrombopoietin gene is not found in patients with nonfamilial essential thrombocythaemia. Br J Haematol 1998;102:1341-3.
    • (1998) Br J Haematol , vol.102 , pp. 1341-1343
    • Harrison, C.N.1    Gale, R.E.2    Wiestner, A.C.3    Skoda, R.C.4    Linch, D.C.5
  • 34
    • 25844453885 scopus 로고    scopus 로고
    • Lessons from familial myeloproliferative disorders
    • Skoda R, Prchal JT. Lessons from familial myeloproliferative disorders. Semin Hematol 2005;42:266-73.
    • (2005) Semin Hematol , vol.42 , pp. 266-273
    • Skoda, R.1    Prchal, J.T.2
  • 35
    • 37049034302 scopus 로고    scopus 로고
    • Familial chronic myeloproliferative disorders: Clinical phenotype and evidence of disease anticipation
    • Rumi E, Passamonti F, Della Porta MG, Elena C, Arcaini L, Vanelli L, et al. Familial chronic myeloproliferative disorders: clinical phenotype and evidence of disease anticipation. J Clin Oncol 2007;25:5630-5.
    • (2007) J Clin Oncol , vol.25 , pp. 5630-5635
    • Rumi, E.1    Passamonti, F.2    Della Porta, M.G.3    Elena, C.4    Arcaini, L.5    Vanelli, L.6
  • 36
    • 38949160429 scopus 로고    scopus 로고
    • Somatic mutations of JAK2 exon 12 in patients with JAK2 (V617F)-negative myeloproliferative disorders
    • Pietra D, Li S, Brisci A, Passamonti F, Rumi E, Theocharides A, et al. Somatic mutations of JAK2 exon 12 in patients with JAK2 (V617F)-negative myeloproliferative disorders. Blood 2008;111:1686-9.
    • (2008) Blood , vol.111 , pp. 1686-1689
    • Pietra, D.1    Li, S.2    Brisci, A.3    Passamonti, F.4    Rumi, E.5    Theocharides, A.6


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