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. Author manuscript; available in PMC: 2008 Apr 17.
Published in final edited form as: Leukemia. 2006 Jul 20;20(9):1572–1581. doi: 10.1038/sj.leu.2404317

Table 1.

Clinical features of pediatric ALL cases evaluated for c-Myc protein stabilization

Patient Age (years) Gender Diagnosis Outcome c-Myc half-life (min) FISH for c-myc
1 6 M Pre-B ALL CCR 91.2 IS
2 3 F Pre-B ALL BM Relapse→death 57.8 2, c-myc; 2 CEP8
3 2 F Pre-B ALL CCR 56.4 2–4, c-myc; 2–4 CEP8a
4 16 M T-cell ALL N/A 44.6 2, c-myc; 2 CEP8
5 2 M Pre-B ALL CCR 31.4 2, c-myc; 2 CEP8
6 4 M T-cell ALL CCR 17.6 IS
Control N/A N/A 19.6b IS

Abbreviations: ALL, acute lymphoblastic leukemia; BM relapse, bone marrow relapse; CCR, continuous complete remission; F, female; FISH, fluorescent in situ hybridization; IS, insufficient sample to perform FISH analysis; M, male; N/A, clinical information not available.

Notes: Age at diagnosis is listed in years. Immunophenotype was determined by flow cytometry at diagnosis for each patient. Measured c-Myc half-life is listed in minutes.

a

Twenty nine of the 100 cells had four signals for c-myc and four for CEP8, indicating tetrasomy 8, 10/100 cells showed trisomy 8 with three signals for c-myc and three for CEP8, 57/100 showed normal two c-myc, two CEP8 and 4/100 showed one c-myc and two CEP8.

b

Representative result of three samples tested (c-Myc half-life range: 17–21 min). (FISH) was performed on 100 interphase cells for each sample.

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