Microsatellite analysis of childhood leukemia: Correlation of 9p and 12p chromosome abnormalities with expression of related genes

被引:4
作者
Nishimura, R [1 ]
Niida, Y [1 ]
Saikawa, Y [1 ]
Goto, Y [1 ]
Noguchi, T [1 ]
Ichihara, T [1 ]
Koizumi, S [1 ]
机构
[1] Kanazawa Univ, Fac Med, Dept Pediat, Kanazawa, Ishikawa 9208641, Japan
关键词
microsatellite; p16; p27/(KIP1); replication error; TEL;
D O I
10.1046/j.1442-200x.1999.01088.x
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background: Loss of heterozygosity (LOH) and DNA replication error (RER) have been thought to be involved in carcinogenesis, but have not been investigated in childhood leukemia and lymphoma. Methods: Eighty samples from 65 patients with childhood leukemia and lymphoma were examined using seven different microsatellite markers for RER analysis. Additionally, LOH in two chromosome regions (9p and 12p) was investigated. Furthermore, expression of the TEL, TEL/AML1 and p27(KIP1) genes on 12p and the p16 gene on 9p were detected by reverse transcriptase polymerase chain reaction. Results: Replication errors were detected in 5/65 patients (7.7%). Most (4/5 patients) RER were preferentially located in the 9p and 12p regions. There were two patients who had DNA abnormalities in both 9p and 12p. one with common acute lymphoblastic leukemia (ALL) showed 9p LOH and the TEL/AML1 fusion gene on 12p and the other with common ALL and 12p RER had diminished expression of both the p27(KIP1) gene on 12p and the p16 gene on 9p. Conclusions: Combined DNA alterations on 9p and 12p, involving LOH, RER and/or gene mutation and chromosomal translocation, were found in childhood acute leukemia, especially in common ALL.
引用
收藏
页码:346 / 352
页数:7
相关论文
共 30 条
  • [1] CLUES TO THE PATHOGENESIS OF FAMILIAL COLORECTAL-CANCER
    AALTONEN, LA
    PELTOMAKI, P
    LEACH, FS
    SISTONEN, P
    PYLKKANEN, L
    MECKLIN, JP
    JARVINEN, H
    POWELL, SM
    JEN, J
    HAMILTON, SR
    PETERSEN, GM
    KINZLER, KW
    VOGELSTEIN, B
    DELACHAPELLE, A
    [J]. SCIENCE, 1993, 260 (5109) : 812 - 816
  • [2] Allelic loss in childhood acute lymphoblastic leukemia
    Baccichet, A
    Qualman, SK
    Sinnett, D
    [J]. LEUKEMIA RESEARCH, 1997, 21 (09) : 817 - 823
  • [3] Cave H, 1996, LEUKEMIA, V10, P1486
  • [4] CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
  • [5] Gartenhaus R, 1996, BLOOD, V87, P38
  • [6] FUSION OF THE TEL GENE ON 12P13 TO THE AML1 GENE ON 21Q22 IN ACUTE LYMPHOBLASTIC-LEUKEMIA
    GOLUB, TR
    BARKER, GF
    BOHLANDER, SK
    HIEBERT, SW
    WARD, DC
    BRAYWARD, P
    MORGAN, E
    RAIMONDI, SC
    ROWLEY, JD
    GILLILAND, DG
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (11) : 4917 - 4921
  • [7] Mutations and loss of expression of a mismatch repair gene, hMLH1, in leukemia and lymphoma cell lines
    Hangaishi, A
    Ogawa, S
    Mitani, K
    Hosoya, N
    Chiba, S
    Yazaki, Y
    Hirai, H
    [J]. BLOOD, 1997, 89 (05) : 1740 - 1747
  • [8] CANDIDATE TUMOR-SUPPRESSOR GENES MTS1 (P16(INK4A)) AND MTS2 (P15(INK4B)) DISPLAY FREQUENT HOMOZYGOUS DELETIONS IN PRIMARY-CELLS FROM T-CELL BUT NOT FROM B-CELL LINEAGE ACUTE LYMPHOBLASTIC LEUKEMIAS
    HEBERT, J
    CAYUELA, JM
    BERKELEY, J
    SIGAUX, F
    [J]. BLOOD, 1994, 84 (12) : 4038 - 4044
  • [9] UBIQUITOUS SOMATIC MUTATIONS IN SIMPLE REPEATED SEQUENCES REVEAL A NEW MECHANISM FOR COLONIC CARCINOGENESIS
    IONOV, Y
    PEINADO, MA
    MALKHOSYAN, S
    SHIBATA, D
    PERUCHO, M
    [J]. NATURE, 1993, 363 (6429) : 558 - 561
  • [10] Kaneko H, 1996, LEUKEMIA, V10, P1696