TRANSCRIPTS OF THE NPM-ALK FUSION GENE IN ANAPLASTIC LARGE-CELL LYMPHOMA, HODGKINS-DISEASE, AND REACTIVE LYMPHOID LESIONS

被引:62
作者
ELMBERGER, PG
LOZANO, MD
WEISENBURGER, DD
SANGER, W
CHAN, WC
机构
[1] UNIV NEBRASKA,MED CTR,DEPT PATHOL & MICROBIOL,OMAHA,NE 68198
[2] UNIV NEBRASKA,MED CTR,DEPT PEDIAT,OMAHA,NE 68198
[3] KAROLINSKA HOSP & INST,DIV CLIN CYTOL,STOCKHOLM,SWEDEN
[4] KAROLINSKA HOSP & INST,DEPT PATHOL & CYTOL,STOCKHOLM,SWEDEN
关键词
D O I
10.1182/blood.V86.9.3517.bloodjournal8693517
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Anaplastic large cell lymphoma (ALCL) and Hodgkin's disease (HD) have some pathologic and immunohistochemical similarities, and a histogenetic relationship between them has been suggested by some investigators. By cytogenetic study, the t(2;5)(p23;q35) translocation appears to be unique for ALCL. The breakpoints of the t(2;5)(p23;q35) have recently been cloned and are reported to involve a novel tyrosine kinase gene, anaplastic lymphoma kinase (alk), on chromosome 2 and the nucleophosmin gene (npm) on chromosome 5. Therefore, we studied the frequency of npm-alk translocation in ALCL using a reverse transcriptase-polymerase chain reaction (RT-PCR) assay. We also studied HD and a variety of reactive lymphoid lesions since there is contradictory information in the literature on the occurrence of the npm-alk rearrangement in HD. We detected npm-alk hybrid mRNA in 8 of 22 cases of ALCL (36%), but none of the 21 cases of HD or the 11 cases with reactive lesions contained amplifiable template. All positive ALCL had the T or indeterminate phenotype and occurred in young adults or children. There was very good correlation between a cytogenetically detectable t(2;5) and a positive signal by RT-PCR. Our results indicate a selective but relatively infrequent association between the t(2;5) and ALCL of T or indeterminate phenotype, not shared with HD or reactive hyperplasia. (C) 1995 by The American Society of Hematology.
引用
收藏
页码:3517 / 3521
页数:5
相关论文
共 25 条
  • [1] KI-1 POSITIVE LARGE CELL LYMPHOMA - A MORPHOLOGIC AND IMMUNOLOGICAL STUDY OF 19 CASES
    AGNARSSON, BA
    KADIN, ME
    [J]. AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1988, 12 (04) : 264 - 274
  • [2] BENZLEMOINE E, 1988, BLOOD, V72, P1045
  • [3] BULLRICH F, 1994, CANCER RES, V54, P2873
  • [4] DELSOL G, 1988, AM J PATHOL, V130, P59
  • [5] MOLECULAR-DETECTION OF THE (2-5) TRANSLOCATION OF NON-HODGKINS-LYMPHOMA BY REVERSE TRANSCRIPTASE-POLYMERASE CHAIN-REACTION
    DOWNING, JR
    SHURTLEFF, SA
    ZIELENSKA, M
    CURCIOBRINT, AM
    BEHM, FG
    HEAD, DR
    SANDLUND, JT
    WEISENBURGER, DD
    KOSSAKOWSKA, AE
    THORNER, P
    LORENZANA, A
    LADANYI, M
    MORRIS, SW
    [J]. BLOOD, 1995, 85 (12) : 3416 - 3422
  • [6] IMMUNOHISTOCHEMICAL, MOLECULAR, AND CYTOGENETIC ANALYSIS OF A CONSECUTIVE SERIES OF 20 PERIPHERAL T-CELL LYMPHOMAS AND LYMPHOMAS OF UNCERTAIN LINEAGE, INCLUDING 12 KI-L POSITIVE LYMPHOMAS
    EBRAHIM, SAD
    LADANYI, M
    DESAI, SB
    OFFIT, K
    JHANWAR, SC
    FILIPPA, DA
    LIEBERMAN, PH
    CHAGANTI, RSK
    [J]. GENES CHROMOSOMES & CANCER, 1990, 2 (01) : 27 - 35
  • [7] ERCOLANI L, 1988, J BIOL CHEM, V263, P15225
  • [8] FRIZZERA G, 1992, SEMIN DIAGN PATHOL, V9, P291
  • [9] IMMUNOGLOBULIN AND T-CELL RECEPTOR GENE REARRANGEMENTS IN HODGKINS-DISEASE AND KI-1-POSITIVE ANAPLASTIC LARGE CELL LYMPHOMA - DISSOCIATION BETWEEN PHENOTYPE AND GENOTYPE
    HERBST, H
    TIPPELMANN, G
    ANAGNOSTOPOULOS, I
    GERDES, J
    SCHWARTING, R
    BOEHM, T
    PILERI, S
    JONES, DB
    STEIN, H
    [J]. LEUKEMIA RESEARCH, 1989, 13 (02) : 103 - +
  • [10] KADIN ME, 1986, BLOOD, V68, P1042