Backtracking of ALL to cord blood

Leukemia Research

Volumn 33, Issue 8, 2009, Pages

  Zuna, Jan ^a   Prouzova, Zuzana ^a   Kalina, Tomas ^a   Lizcova, Libuse ^a   Zemanova, Zuzana ^a   Muzikova, Katerina ^a   Rahmatova, Sarka ^b   Meijerink, Jules P P ^c   Trka, Jan ^a  

^a CHARLES UNIVERSITY   (Czech Republic)

^b INSTITUTE OF HEMATOLOGY AND BLOOD TRANSFUSION   (Czech Republic)

^c SOPHIA CHILDREN S HOSPITAL   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

NOTCH1 RECEPTOR;

ACUTE LYMPHOBLASTIC LEUKEMIA; BONE MARROW; CASE REPORT; CELL SELECTION; CHILD; CHROMOSOME; CLINICAL FEATURE; EXON; GENE MUTATION; HUMAN; IMMUNOGLOBULIN HEAVY CHAIN GENE; IMMUNOPHENOTYPING; LETTER; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; PRIORITY JOURNAL; RELAPSE; UMBILICAL CORD BLOOD;

CHILD, PRESCHOOL; FEMALE; FETAL BLOOD; FETAL DISEASES; HUMANS; MALE; NEOPLASM PROTEINS; NEOPLASTIC STEM CELLS; PRECURSOR B-CELL LYMPHOBLASTIC LEUKEMIA-LYMPHOMA;

EID: 67349214705     PISSN: 01452126     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.leukres.2009.01.013     Document Type: Letter

References (11)

1. Greaves M. In utero origins of childhood leukaemia. Early Hum Dev. 81 January (1) (2005) 123-129
2. Fischer S., Mann G., Konrad M., Metzler M., Ebetsberger G., Jones N., et al. Screening for leukemia- and clone-specific markers at birth in children with T-cell precursor ALL suggests a predominantly postnatal origin. Blood 110 October (8) (2007) 3036-3038
3. Gale K.B., Ford A.M., Repp R., Borkhardt A., Keller C., Eden O.B., et al. Backtracking leukemia to birth: identification of clonotypic gene fusion sequences in neonatal blood spots. Proc Natl Acad Sci USA 94 December (25) (1997) 13950-13954
4. Wiemels J.L., Cazzaniga G., Daniotti M., Eden O.B., Addison G.M., Masera G., et al. Prenatal origin of acute lymphoblastic leukaemia in children. Lancet 354 October (9189) (1999) 1499-1503
5. Wiemels J.L., Xiao Z., Buffler P.A., Maia A.T., Ma X., Dicks B.M., et al. In utero origin of t(8;21) AML1-ETO translocations in childhood acute myeloid leukemia. Blood 99 May (10) (2002) 3801-3805
6. Eguchi-Ishimae M., Eguchi M., Kempski H., and Greaves M. NOTCH1 mutation can be an early, prenatal genetic event in T-ALL. Blood 111 January (1) (2008) 376-378
7. Maia A.T., Tussiwand R., Cazzaniga G., Rebulla P., Colman S., Biondi A., et al. Identification of preleukemic precursors of hyperdiploid acute lymphoblastic leukemia in cord blood. Genes Chrom Cancer 40 1 (2004 May) 38-43
8. Moorman A.V., Richards S.M., Martineau M., Cheung K.L., Robinson H.M., Jalali G.R., et al. Outcome heterogeneity in childhood high-hyperdiploid acute lymphoblastic leukemia. Blood 102 October (8) (2003) 2756-2762
9. Gruhn B., Taub J.W., Ge Y., Beck J.F., Zell R., Hafer R., et al. Prenatal origin of childhood acute lymphoblastic leukemia, association with birth weight and hyperdiploidy. Leukemia 22 September (9) (2008) 1692-1697
10. Maia A.T., van der Velden V.H., Harrison C.J., Szczepanski T., Williams M.D., Griffiths M.J., et al. Prenatal origin of hyperdiploid acute lymphoblastic leukemia in identical twins. Leukemia 17 November (11) (2003) 2202-2206
11. Panzer-Grumayer E.R., Fasching K., Panzer S., Hettinger K., Schmitt K., Stockler-Ipsiroglu S., et al. Nondisjunction of chromosomes leading to hyperdiploid childhood B-cell precursor acute lymphoblastic leukemia is an early event during leukemogenesis. Blood 100 July (1) (2002) 347-349