Clonality analysis of hematopoiesis in essential thrombocythemia: Advantages of studying T lymphocytes and platelets

Blood

Volumn 89, Issue 1, 1997, Pages 128-134

  El Kassar, Nahed ^a   Hetet, Gilles ^b   Brière, Jean ^b   Grandchamp, Bernard ^b  

^a INSERM   (France)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; CLINICAL ARTICLE; CLONOGENESIS; CONTROLLED STUDY; DNA METHYLATION; FEMALE; HUMAN; HUMAN CELL; PRIORITY JOURNAL; T LYMPHOCYTE; THROMBOCYTE; THROMBOCYTHEMIA; THROMBOCYTOSIS; X CHROMOSOME INACTIVATION;

EID: 0031019581     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v89.1.128     Document Type: Article

References (28)

1. Murphy S, Hand H, Rosenthal D, Laszlo J: Essential thrombocythemia: An interim report from the Polycythemia Vera Study Group. Blood 23:177, 1986
2. Dudley JM, Messinezy M, Eridani M, Holland LJ, Lawrie A, Nunan TO, Sawyer B, Savidge GF, Pearson TC: Primary thrombocythemia: Diagnosis criteria and a simple scoring system for positive diagnosis. Br J Haematol 71:331, 1989
3. Han ZC, Brière J, Abgrall JF, Sensèbe L, Nedellec G, Parent D, Guern G: Spontaneous formation of megakaryocyte progenitors (CFU-MK) in primary thrombocythaemia. Acta Haematol 78:51, 1987
4. Pearson TC: Primary thrombocythemia: Diagnosis and management. Br J Haematol 78:145. 1991
5. Lyon MF: Gene action in the X chromosome of the mouse. Nature 190:372, 1961
6. Fialkow PJ, Faguet GB, Jacobson RJ, Vaidya K, Murphy S: Evidence that essential thrombocythemia is a clonal disorder with origin in a multipotent stem cell. Blood 58:916, 1981
7. Meditarranean subjects. Blood 59:76, 1982
8. Raskind WH, Jacobson R, Murphy S, Adamson JW, Fialkow PJ: Evidence for the involvement of B lymphoid cells in polycythemia vera and essential thrombocythemia. J Clin Invest 75:1388, 1985
9. Vogelstein B, Fearon ER, Hamilton SR, Feinberg AP: Use of restriction fragment length polymorphisms to determine the clonal origin of human tumors. Science 227:642, 1985
10. Gilliland DG, Blanchard KL, Levy J, Perrin S, Bunn HF: Clonality in myeloproliferative disorders. Proc Natl Acad Sci USA 88:6848, 1991
11. Jinnai I, Yoshida S, Toyoda A, Murohashi I, Bessho M, Hirashima K, Nagai K, Tomonaga M, Boyd Y: A clonal study of hematopoiesis using the M27 b probe: Abberant band patterns caused by incomplete digestion of a methyl-sensitive enzyme in the inactive X-chromosome. Leukemia 7:1432, 1993
12. Fey MF, Liechti-Gallati S, Von Rohr A, Borisch B, Theilkâs L, Schneider V, Oestreicher M, Nagel S, Ziemiecki A, Tobler A: Clonality and X-inactivation patterns in hematopoietic cell popula-tions detected by highly informative M27b DNA probe. Blood 83:931, 1994
13. Allen RC, Zoghbi HY, Moseley AB, Rosenblatt HM, Belmont JW: Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation. Am J Hum Genet 51:1229. 1992
14. El Kassar N, Hetet G, LI Y, Brière J, Grandchamp B: Clonal analysis of haematopoietic cells in essential thrombocythaemia. Br J Haematol 90:131. 1995
15. Ann K, Ito M, Misawa M, Ohe Y, Kai S, Kohsaki M, Hara H: Clonal analysis of peripheral blood and haemopoíetic colonies in patients with aplastic anaemia and refractory anaemia using the polymorphic short tandem repeat on the human androgen-receptor (HUMARA) gene. Br J Haematol 89:838. 1995
16. Lucas GS, Padua RA, Masters GS, Oscier DG, Jacobs A: The application of X-chromosome gene probes to the diagnosis of myeloproliferative disease. Br J Haematol 72:530. 1989
17. Anger B, Janssen JWG, Schrezenmeier H, Hehlmann R, Heimpel H, Bartram CR: Clonal analysis of chronic myeloproliferative disorders using X-linked DNA polymorphisms. Leukemia 4:258, 1990
18. Janssen JWG, Anger BR, Drexler HG, Bartram CR, Heimpel H: Essential thrombocythemia in two sisters originating from different stem cell levels. Blood 75:1633, 1990
19. Turhan AG, Cashman JD, Eaves CJ, Humphries RK, Eaves AC: Variable expression of features of normal and neoplastic stem cells in patients with thrombocytosis. Br J Haematol 82:50, 1992
20. Tsukamoto N, Morita K, Maehara T, Okamoto K, Sakai H: Clonality in chronic myeloproliferative disorders defined by X-chromosome linked probes: Demonstration of heterogeneity in lineage involvement. Br J Haematol 86:253, 1994
21. Prchal JT, Guan YL: A novel clonality assay based on transcriptional analysis of the active X-chromosome. Stem Cells 11:62, 1993
22. Prchal JT, Liu Y, Prchal JF, Hoffman R, Tushinski R: Are normal stem cells present in myeloproliferative syndrome? Blood 84:207, 1994 (abstr, suppl 1)
23. Bunge S, Steglich C, Zuther C, Beck M, Morris CP, Schwinger E, Schinzel A, Hopwood JH, Gal A: Iduronate-2-sulfatase gene mutations in 16 patients with mucopolysaccharidosis type II (Hunter syndrome). Hum Molec Genet 2:1871, 1993
24. Chomzynski P, Sacchi N: Single-step method of RNA isolation by acid guanidium thiocyanate-phenol-chloroform extraction. Anal Biochem 162:156, 1989
25. Delfau MH, Kerkaert JP, Collyn d'Hooghe G, Fenaux P, Lai JL, Jouet JP, Grandchamp B: Detection of minimal residual disease in chronic myeloid leukemia patients after bone marrow transplantation by polymerase chain reaction. Leukemia 4:1, 1990
26. Tan SS, Williams EA, Tam PPL: X-chromosome inactivation occurs at different times in different tissues of the post-implantation mouse embryon. Nature Genet 3:170, 1993
27. Gale R, Wheadon H, Boulos P, Linch DC: Tissue specificity of X-chromosome inactivation patterns. Blood 83:2899, 1994
28. Prchal JT, Prchal JF: Evolving understanding of cellular defect in polycythemia vera: Implications for its clinical diagnosis and molecular pathophysiology. Blood 83:1, 1994