FREQUENT EXPRESSION OF FAS/APO-1 IN HODGKINS-DISEASE AND ANAPLASTIC LARGE-CELL LYMPHOMAS

被引:54
作者
XERRI, L
CARBUCCIA, N
PARC, P
HASSOUN, J
BIRG, F
机构
[1] INSERM,U119,F-13009 MARSEILLE,FRANCE
[2] INST J PAOLI I CALMETTES,ANAT PATHOL LAB,F-13009 MARSEILLE,FRANCE
关键词
FAS/APO-1; HODGKINS DISEASE; NON-HODGKINS LYMPHOMA;
D O I
10.1111/j.1365-2559.1995.tb00215.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
FAS/APO-1 (CD95) is a membrane glycoprotein belonging to the tumour necrosis factor/nerve growth factor receptor family, and which can trigger apoptosis in some lymphoid cell lines, Immunohistochemistry combined with Northern blotting allowed determination of the pattern of FAS/APO-1 expression in a series of Ki-1 [CD30] positive lymphoid malignancies, including 27 Hodgkin's disease and eight anaplastic large cell lymphomas. CD30 negative tumours used as controls included 27 B-cell non-Hodgkin's lymphomas, 14 T-cell non-Hodgkin's lymphomas, four reactive lymphadenitis, and non-lymphoid tissues, Immunohistochemistry, performed on frozen sections, revealed a strong FAS/APO-1 expression in 25 out of 27 (92%) Hodgkin's disease cases, predominantly in Reed Sternberg cells; 50 to 100% of the neoplastic cells in eight out of (100%) anaplastic large cell lymphoma cases were positive, In contrast, positive FAS/APO-1 immunostaining was observed only in 22 out of 41 (53%) CD30 negative non-Hodgkin's lymphomas, Northern blot analysis detected variable amounts of the FAS/APO-1 transcript in the immunohistochemistry-positive samples. These results suggest possible hyper-expression of FAS/APO-1 (CD95) in Hodgkin's disease and anaplastic large cell lymphomas.
引用
收藏
页码:235 / 241
页数:7
相关论文
共 38 条
  • [11] THE POLYPEPTIDE ENCODED BY THE CDNA FOR HUMAN CELL-SURFACE ANTIGEN FAS CAN MEDIATE APOPTOSIS
    ITOH, N
    YONEHARA, S
    ISHII, A
    YONEHARA, M
    MIZUSHIMA, S
    SAMESHIMA, M
    HASE, A
    SETO, Y
    NAGATA, S
    [J]. CELL, 1991, 66 (02) : 233 - 243
  • [12] EXPRESSION AND STRUCTURE OF THE HUMAN NGF RECEPTOR
    JOHNSON, D
    LANAHAN, A
    BUCK, CR
    SEHGAL, A
    MORGAN, C
    MERCER, E
    BOTHWELL, M
    CHAO, M
    [J]. CELL, 1986, 47 (04) : 545 - 554
  • [13] KONDO E, 1994, AM J PATHOL, V145, P330
  • [14] EXPRESSION OF FUNCTIONAL FAS ANTIGEN ON ADULT T-CELL LEUKEMIA
    KOTANI, T
    ARATAKE, Y
    KONDO, S
    TAMURA, K
    OHTAKI, S
    [J]. LEUKEMIA RESEARCH, 1994, 18 (04) : 305 - 310
  • [15] REGULATION OF APOPTOSIS IN THE IMMUNE-SYSTEM
    KRAMMER, PH
    BEHRMANN, I
    DANIEL, P
    DHEIN, J
    DEBATIN, KM
    [J]. CURRENT OPINION IN IMMUNOLOGY, 1994, 6 (02) : 279 - 289
  • [16] KRAMMER PH, 1992, CURR BIOL, V7, P383
  • [17] LEITHAUSER F, 1993, LAB INVEST, V69, P415
  • [18] THE HUMAN APO-1 (APT) ANTIGEN MAPS TO 10Q23, A REGION THAT IS SYNTENIC WITH MOUSE CHROMOSOME-19
    LICHTER, P
    WALCZAK, H
    WEITZ, S
    BEHRMANN, I
    KRAMMER, PH
    [J]. GENOMICS, 1992, 14 (01) : 179 - 180
  • [19] THE MOUSE FAS-LIGAND GENE IS MUTATED IN GLD MICE AND IS PART OF A TNF FAMILY GENE-CLUSTER
    LYNCH, DH
    WATSON, ML
    ALDERSON, MR
    BAUM, PR
    MILLER, RE
    TOUGH, T
    GIBSON, M
    DAVISSMITH, T
    SMITH, CA
    HUNTER, K
    BHAT, D
    DIN, W
    GOODWIN, RG
    SELDIN, MF
    [J]. IMMUNITY, 1994, 1 (02) : 131 - 136
  • [20] CHARACTERIZATION OF THE MRC OX40 ANTIGEN OF ACTIVATED CD4 POSITIVE LYMPHOCYTES-T - A MOLECULE RELATED TO NERVE GROWTH-FACTOR RECEPTOR
    MALLETT, S
    FOSSUM, S
    BARCLAY, AN
    [J]. EMBO JOURNAL, 1990, 9 (04) : 1063 - 1068