Conditions associated with antibodies against the tumor-associated antigen MUC1 and their relationship to risk for ovarian cancer

被引:100
作者
Cramer, DW
Titus-Ernstoff, L
McKolanis, JR
Welch, WR
Vitonis, AF
Berkowitz, RS
Finn, OJ
机构
[1] Brigham & Womens Hosp, Ob Gyn Epiemiol Ctr, Dept Pathol, Womens & Perinatal Pathol Div, Boston, MA 02115 USA
[2] Brigham & Womens Hosp, Ob Gyn Epiemiol Ctr, Dept Obstet & Gynecol, Div Gynecol Oncol, Boston, MA 02115 USA
[3] Dartmouth Hitchcock Med Ctr, Norris Cotton Canc Ctr, Lebanon, NH 03766 USA
[4] Univ Pittsburgh, Sch Med, Dept Immunol, Pittsburgh, PA USA
关键词
D O I
10.1158/1055-9965.EPI-05-0035
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Many cancers, including ovarian, overexpress epithelial mucin (MUC1) and promote anti-MUC1 antibodies that may correlate with more favorable prognosis. By extension, risk for ovarian cancer might be reduced by preexisting MUC1-specific immunity. We measured anti-MUC1 antibodies in 705 control women, identified events predicting antibodies, and estimated ovarian cancer risk by comparing profiles of events generating antibodies in controls with those in 668 ovarian cancer cases. Factors predicting antibodies included oral contraceptive use, breast mastitis, bone fracture or osteoporosis, pelvic surgeries, nonuse of talc in genital hygiene, and to a lesser extent intrauterine device use and current smoking. There was a significant increase in the likelihood of having anti-MUC1 antibodies from 24.2% in women with 0 or 1 condition, to 51.4% in those with five or more conditions. By the same index of events, the risk for ovarian cancer was inversely associated with number of conditions predisposing to anti-MUC1 antibodies. Compared with having experienced 0 or 1 event, the adjusted risk for ovarian cancer decreased progressively with relative risks (and 95% confidence limits) of 0.69 (0.52-0.92), 0.64 (0.47-0.88), 0.49 (0.34-0.72), and 0.31 (0.16-0.61), respectively for women with two, three, four, and five or more events related to the presence of antibodies (P-trend < 0.0001.) We conclude that several traditional and new risk factors for ovarian cancer may be explained by their ability to induce MUC1 immunity through exposure of MUC1 to immune recognition in the context of inflammatory or hormonal processes in various MUC1-positive tissues.
引用
收藏
页码:1125 / 1131
页数:7
相关论文
共 48 条
  • [1] AGRAWAL B, 1995, CANCER RES, V55, P2257
  • [2] Agrawal B, 1996, J IMMUNOL, V157, P2089
  • [3] Maternal serum CA125 and CA15-3 antigen levels in normal and pathological pregnancy
    Bon, GG
    Kenemans, P
    Verstraeten, AA
    Go, S
    Philipi, PA
    van Kamp, GJ
    van Geijn, HP
    van Vugt, JMG
    [J]. FETAL DIAGNOSIS AND THERAPY, 2001, 16 (03) : 166 - 172
  • [4] CIGARETTE-SMOKING AND THE RISK OF ENDOMETRIAL CANCER
    BRINTON, LA
    BARRETT, RJ
    BERMAN, ML
    MORTEL, R
    TWIGGS, LB
    WILBANKS, GD
    [J]. AMERICAN JOURNAL OF EPIDEMIOLOGY, 1993, 137 (03) : 281 - 291
  • [5] Expression of MUC-1 epitopes on normal bone marrow:: Implications for the detection of micrometastatic tumor cells
    Brugger, W
    Bühring, HJ
    Grünebach, F
    Vogel, W
    Kaul, S
    Müller, R
    Brümmendorf, TH
    Ziegler, BL
    Rappold, I
    Brossart, P
    Scheding, S
    Kanz, L
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (05) : 1535 - 1544
  • [6] CRAMER DE, 1983, NATL CANC I, V1, P717
  • [7] Cramer DW, 1999, INT J CANCER, V81, P351, DOI 10.1002/(SICI)1097-0215(19990505)81:3<351::AID-IJC7>3.0.CO
  • [8] 2-M
  • [9] Detection of circulating mammary mucin (MUC1) and MUC1 immune complexes (MUC1-CIC) in healthy women
    Croce, MV
    Isla-Larrain, MT
    Price, MR
    Segal-Eiras, A
    [J]. INTERNATIONAL JOURNAL OF BIOLOGICAL MARKERS, 2001, 16 (02) : 112 - 120
  • [10] Matrix metalloproteinases production in malignant pleural effusions after talc pleurodesis
    D'Agostino, P
    Camemi, AR
    Caruso, R
    Arcoleo, F
    Cascio, A
    Dolce, A
    Sacco, E
    Cangemi, G
    Di Rosa, T
    Moceo, P
    Cillari, E
    [J]. CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2003, 134 (01) : 138 - 142