Prognostic significance of a combination of soluble Fas and soluble Fas ligand in the serum of patients with Ta bladder cancer

被引:22
作者
Mizutani, Y [1 ]
Yoshida, O
Ukimura, O
Kawauchi, A
Bonavida, B
Miki, T
机构
[1] Kyoto Prefectural Univ, Dept Urol, Kamigyo Ku, Kyoto 6028566, Japan
[2] Kyoto Univ, Grad Sch Med, Fac Med, Dept Urol, Kyoto 6068507, Japan
[3] Univ Calif Los Angeles, Sch Med, Dept Microbiol Immunol & Mol Genet, Los Angeles, CA 90095 USA
关键词
sFas; sFasL; Fas; FasL; bladder cancer; recurrence;
D O I
10.1089/108497802760804790
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Recurrence after transurethral resection is one of the major problems in the treatment of superficial bladder cancer. However, there are no potent prognostic markers for recurrence in superficial bladder cancer at present. As circulating soluble Fas (sFas) and soluble Fas ligand (sFasL) have been implicated in protection from Fas-mediated apoptosis against cancers and may interfere with immune surveillance against autologous cancers, sFas and sFasL in the serum of patients with Ta bladder cancer were evaluated as prognostic tumor markers for recurrence. The serum levels of sFas and sFasL were measured by an enzyme-linked immunosorbent assay. Patients with Ta bladder cancer with low serum levels of both sFas and sFasL had a significantly longer postoperative tumor free interval than those with high serum level of either sFas or sFasL in the 3-year follow-up. There was no correlation between the serum levels of sFas and sFasL. The present study has demonstrated that elevated serum sFas or sFasL predicts early recurrence in patients with Ta bladder cancer. These findings suggest that the serum levels of sFas and sFasL can be used as a prognostic indicator for recurrence in patients with Ta bladder cancer, and that sFas and sFasL may independently inhibit Fas-mediated apoptosis.
引用
收藏
页码:563 / 567
页数:5
相关论文
共 19 条
  • [1] FAS-MEDIATED CYTOTOXICITY BY FRESHLY ISOLATED NATURAL-KILLER-CELLS
    ARASE, H
    ARASE, N
    SAITO, T
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 181 (03) : 1235 - 1238
  • [2] Bellone G, 2000, CLIN CANCER RES, V6, P2448
  • [3] 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
  • [4] FAS AND PERFORIN PATHWAYS AS MAJOR MECHANISMS OF T-CELL-MEDIATED CYTOTOXICITY
    KAGI, D
    VIGNAUX, F
    LEDERMANN, B
    BURKI, K
    DEPRAETERE, V
    NAGATA, S
    HENGARTNER, H
    GOLSTEIN, P
    [J]. SCIENCE, 1994, 265 (5171) : 528 - 530
  • [5] METALLOPROTEINASE-MEDIATED RELEASE OF HUMAN FAS LIGAND
    KAYAGAKI, N
    KAWASAKI, A
    EBATA, T
    OHMOTO, H
    IKEDA, S
    INOUE, S
    YOSHINO, K
    OKUMURA, K
    YAGITA, H
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 182 (06) : 1777 - 1783
  • [6] Lamm D L, 1995, Int J Urol, V2 Suppl 2, P23, DOI 10.1111/j.1442-2042.1995.tb00476.x
  • [7] Prognostic significance of soluble Fas in the serum of patients with bladder cancer
    Mizutani, Y
    Yoshida, O
    Bonavida, B
    [J]. JOURNAL OF UROLOGY, 1998, 160 (02) : 571 - 576
  • [8] Mizutani Y, 2001, CANCER, V92, P287, DOI 10.1002/1097-0142(20010715)92:2<287::AID-CNCR1321>3.0.CO
  • [9] 2-4
  • [10] THE FAS DEATH FACTOR
    NAGATA, S
    GOLSTEIN, P
    [J]. SCIENCE, 1995, 267 (5203) : 1449 - 1456