Death-associated protein kinase loss of expression is a new marker for breast cancer prognosis

被引:27
作者
Lévy, D
Plu-Bureau, G
Decroix, Y
Hugol, D
Rostène, W
Kimchi, A
Gompel, A
机构
[1] Hop Hotel Dieu, Unite Gynecol Endocrinienne, F-75004 Paris, France
[2] Hop Hotel Dieu, Dept Pathol Anat, F-75004 Paris, France
[3] Hop St Antoine, INSERM, U339, F-75571 Paris, France
[4] Weizmann Inst Sci, Dept Mol Genet, IL-76100 Rehovot, Israel
关键词
D O I
10.1158/1078-0432.CCR-03-0213
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Death-associated protein (DAP)-kinase is a new Ser/Thr kinase involved in cell apoptosis and tumor suppression, the expression of which has been correlated to invasive potential and metastasis in several human neoplastic tissues. We analyzed the level of DAP-kinase expression in breast cancer specimens and its correlation with survival. Experimental Design: One hundred twenty-eight breast cancer specimens were analyzed by immunohistochemistry. Patient records were studied retrospectively for demographic characteristics, clinical data, hormonal treatment, outcome, and survival. DAP-kinase protein expression was also studied in normal breast cells primary cultures under estrogen and antiestrogen treatment. Results: Among the 128 patients, 30 showed a DAP-kinase staining less than or equal to 20%, whereas 98 had a staining over 20%. Mean follow-up time was 62 months. The association between tumor Scarff-Bloom and Richardson grade (P = 0.009), estrogen receptor and progesterone receptor expression (P = 0.002 and 0.001, respectively), tumor size (P = 0.05), Bcl-2 expression (P = 0.004), and DAP-kinase immu-nostaining in the ductal carcinoma group was highly significant. Overall (64 months) and disease-free (63 months) survival in the high DAP-kinase expression group were significantly longer compared with the women whose tumors showed a loss of DAP-kinase expression (51 and 43 months, respectively). DAP-kinase protein was strongly expressed in normal breast tissue and in human breast epithelial cells primary cultures. Estradiol decreased DAP-kinase expression in these cells, arguing for hormonal regulation of the protein. Conclusions: Loss of DAP-kinase expression negatively correlates to survival and positively correlates to the prob-ability of recurrence in a very significant manner. DAP-kinase thus constitutes a novel and independent prognosis marker for breast cancer.
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页码:3124 / 3130
页数:7
相关论文
共 22 条
  • [1] DAP-kinase: from functional gene cloning to establishment of its role in apoptosis and cancer
    Cohen, O
    Kimchi, A
    [J]. CELL DEATH AND DIFFERENTIATION, 2001, 8 (01) : 6 - 15
  • [2] DAP-kinase is a Ca2+ calmodulin-dependent, cytoskeletal-associated protein kinase, with cell death-inducing functions that depend on its catalytic activity
    Cohen, O
    Feinstein, E
    Kimchi, A
    [J]. EMBO JOURNAL, 1997, 16 (05) : 998 - 1008
  • [3] APOPTOSIS IN ANTITUMOR STRATEGIES - MODULATION OF CELL-CYCLE OR DIFFERENTIATION
    DARZYNKIEWICZ, Z
    [J]. JOURNAL OF CELLULAR BIOCHEMISTRY, 1995, 58 (02) : 151 - 159
  • [4] IDENTIFICATION OF A NOVEL SERINE THREONINE KINASE AND A NOVEL 15-KD PROTEIN AS POTENTIAL MEDIATORS OF THE GAMMA-INTERFERON-INDUCED CELL-DEATH
    DEISS, LP
    FEINSTEIN, E
    BERISSI, H
    COHEN, O
    KIMCHI, A
    [J]. GENES & DEVELOPMENT, 1995, 9 (01) : 15 - 30
  • [5] Falette N, 1998, CANCER RES, V58, P1451
  • [6] PROGESTIN EFFECT ON CELL-PROLIFERATION AND 17-BETA-HYDROXYSTEROID DEHYDROGENASE-ACTIVITY IN NORMAL HUMAN-BREAST CELLS IN CULTURE
    GOMPEL, A
    MALET, C
    SPRITZER, P
    LALARDRIE, JP
    KUTTENN, F
    MAUVAISJARVIS, P
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1986, 63 (05) : 1174 - 1180
  • [7] Hormonal regulation of apoptosis in breast cells and tissues
    Gompel, A
    Somai, S
    Chaouat, M
    Kazem, A
    Kloosterboer, HJ
    Beusman, I
    Forgez, P
    Mimoun, M
    Rostène, W
    [J]. STEROIDS, 2000, 65 (10-11) : 593 - 598
  • [8] DAP kinase links the control of apoptosis to metastasis
    Inbal, B
    Cohen, O
    PolakCharcon, S
    Kopolovic, J
    Vadai, E
    Eisenbach, L
    Kimchi, A
    [J]. NATURE, 1997, 390 (6656) : 180 - 184
  • [9] Kandouz M, 1996, INT J CANCER, V68, P120, DOI 10.1002/(SICI)1097-0215(19960927)68:1<120::AID-IJC21>3.0.CO
  • [10] 2-E