Circulating Inflammation Markers and Risk of Epithelial Ovarian Cancer

被引:96
作者
Clendenen, Tess V. [1 ]
Lundin, Eva [4 ,5 ]
Zeleniuch-Jacquotte, Anne [3 ]
Koenig, Karen L.
Berrino, Franco [9 ]
Lukanova, Annekatrin [2 ,10 ]
Lokshin, Anna E. [11 ,12 ,13 ]
Idahl, Annika [6 ,7 ]
Ohlson, Nina [4 ,5 ]
Hallmans, Goran [8 ]
Krogh, Vittorio
Sieri, Sabina
Muti, Paola [14 ]
Marrangoni, Adele [11 ]
Nolen, Brian M. [11 ]
Liu, Mengling
Shore, Roy E. [15 ]
Arslan, Alan A. [2 ,3 ]
机构
[1] NYU, Sch Med, Div Epidemiol, Dept Environm Med, New York, NY 10003 USA
[2] NYU, Sch Med, Dept Obstet & Gynecol, New York, NY USA
[3] NYU, Sch Med, New York Univ Canc Inst, New York, NY USA
[4] Umea Univ, Dept Med Biosci, Umea, Sweden
[5] Umea Univ, Dept Pathol, S-90187 Umea, Sweden
[6] Umea Univ, Dept Clin Sci, Umea, Sweden
[7] Umea Univ, Dept Obstet & Gynecol, Umea, Sweden
[8] Umea Univ, Dept Publ Hlth & Clin Med Nutrit Res, Umea, Sweden
[9] Natl Canc Inst, Etiol & Prevent Epidemiol Unit, I-20133 Milan, Italy
[10] German Canc Res Ctr, Div Canc Epidemiol, Heidelberg, Germany
[11] Univ Pittsburgh, Dept Med, Univ Pittsburgh Canc Inst, Div Canc Prevent & Populat Sci, Pittsburgh, PA USA
[12] Univ Pittsburgh, Dept Pathol, Pittsburgh, PA USA
[13] Univ Pittsburgh, Dept Ob Gyn Reprod Sci, Pittsburgh, PA USA
[14] Natl Canc Inst, Nutr Epidemiol Unit, I-20133 Milan, Italy
[15] Radiat Effects Res Fdn, Hiroshima, Japan
关键词
NORMAL MENSTRUAL-CYCLE; SOLUBLE CYTOKINE RECEPTORS; SEX-HORMONE LEVELS; BREAST-CANCER; DIFFERENTIAL EXPRESSION; UTERINE ARTERIES; LEVELS CORRELATE; BLOOD-FLOW; IN-VIVO; INTERLEUKIN-6;
D O I
10.1158/1055-9965.EPI-10-1180
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Background: Factors contributing to chronic inflammation appear to be associated with increased risk of ovarian cancer. The purpose of this study was to assess the association between circulating levels of inflammation mediators and subsequent risk of ovarian cancer. Methods: We conducted a case-control study of 230 cases and 432 individually matched controls nested within three prospective cohorts to evaluate the association of prediagnostic circulating levels of inflammation-related biomarkers (IL-1 beta, IL-2, IL-4, IL-5, IL-6, IL-10, IL-12p40, IL-12p70, IL-13, TNF alpha, IL-1Ra, sIL-1RII, sIL-2Ra, sIL-4R, sIL-6R, sTNF-R1, and sTNF-R2) measured using Luminex xMap technology with risk of ovarian cancer. Results: We observed a trend across quartiles for IL-2 (ORQ4 vs. Q1: 1.57, 95% CI: 0.98-2.52, P = 0.07), IL-4 (ORQ4 vs. Q1: 1.50, 95% CI: 0.95-2.38, P = 0.06), IL-6 (ORQ4 vs. Q1: 1.63, 95% CI: 1.03-2.58, P = 0.03), IL-12p40 (ORQ4 vs. Q1: 1.60, 95% CI: 1.02-2.51, P = 0.06), and IL-13 (ORQ4 vs. Q1: 1.42, 95% CI: 0.90-2.26, P = 0.11). Trends were also observed when cytokines were modeled on the continuous scale for IL-4 (P trend = 0.01), IL-6 (P trend = 0.01), IL-12p40 (P trend = 0.01), and IL-13 (P trend = 0.04). ORs were not materially different after excluding cases diagnosed less than 5 years after blood donation or when limited to serous tumors. Conclusions and Impact: This study provides the first direct evidence that multiple inflammation markers, specifically IL-2, IL-4, IL-6, IL-12, and IL-13, may be associated with risk of epithelial ovarian cancer, and adds to the evidence that inflammation is involved in the development of this disease. Cancer Epidemiol Biomarkers Prev; 20(5); 799-810. (C)2011 AACR.
引用
收藏
页码:799 / 810
页数:12
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