Channing Laboratory, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts 02115, USA.
Cancer Epidemiol Biomarkers Prev. 2010 Jun;19(6):1595-601. doi: 10.1158/1055-9965.EPI-10-0068. Epub 2010 May 25.
The surface epithelial glycoprotein MUC1 becomes overexpressed and hypoglycosylated in adenocarcinomas; similar changes occur during nonmalignant inflammatory events. Antibodies developed against tumor-like MUC1 in response to such events could be one way through which ovarian cancer risk factors operate.
We evaluated the association between anti-MUC1 antibodies and risk of ovarian cancer in a prospective nested case-control study in the Nurses' Health Studies. We used an ELISA to measure plasma anti-MUC1 antibodies in 117 ovarian cancer cases collected at least 3 years before diagnosis and 339 matched controls.
In controls, younger women (P-trend = 0.03), those with a tubal ligation (P = 0.03), and those with fewer ovulatory cycles (P-trend = 0.04) had higher antibody levels. In cases, women with late-stage disease (P = 0.04) and those whose specimen was >11 years remote from diagnosis (P = 0.01) had higher antibody levels. Overall, increasing anti-MUC1 antibody levels were associated with a nonsignificant trend for lower risk for ovarian cancer, but there was highly significant heterogeneity by age (P-heterogeneity = 0.005). In women <64 years, the antibody level in quartiles 2 to 4 versus quartile 1 were associated with reduced risk (relative risk = 0.53; 95% confidence interval, 0.31-0.93; P-trend = 0.03), whereas in women > or = 64 years, the corresponding relative risk was 2.11 (95% confidence interval, 0.73-6.04); P-trend = 0.05).
Anti-MUC1 antibodies evaluated several years before diagnosis may be associated with lower risk of subsequent ovarian cancer in women <64 years old at assessment.
Key elements of an "immune model" to explain ovarian cancer risk factors are confirmed and should be evaluated in larger prospective studies.
表面上皮糖蛋白 MUC1 在腺癌中过度表达和低聚糖化;在非恶性炎症事件中也会发生类似的变化。针对此类事件,针对肿瘤样 MUC1 产生的抗体可能是卵巢癌危险因素作用的一种方式。
我们在护士健康研究中的一项前瞻性巢式病例对照研究中评估了抗-MUC1 抗体与卵巢癌风险之间的关联。我们使用 ELISA 测量了至少在诊断前 3 年收集的 117 例卵巢癌病例和 339 例匹配对照者的血浆抗-MUC1 抗体。
在对照组中,年轻女性(P 趋势= 0.03)、接受输卵管结扎术的女性(P = 0.03)和排卵周期较少的女性(P 趋势= 0.04)的抗体水平较高。在病例组中,晚期疾病患者(P = 0.04)和标本距诊断 > 11 年的患者(P = 0.01)的抗体水平较高。总体而言,抗-MUC1 抗体水平升高与卵巢癌风险降低呈非显著趋势相关,但按年龄存在高度显著的异质性(P 异质性= 0.005)。在<64 岁的女性中,第 2 至 4 四分位与第 1 四分位相比,抗体水平与降低的风险相关(相对风险= 0.53;95%置信区间,0.31-0.93;P 趋势= 0.03),而在>或= 64 岁的女性中,相应的相对风险为 2.11(95%置信区间,0.73-6.04);P 趋势= 0.05)。
在评估时<64 岁的女性中,在诊断前数年评估的抗-MUC1 抗体可能与随后的卵巢癌风险降低相关。
解释卵巢癌危险因素的“免疫模型”的关键要素得到了证实,应在更大的前瞻性研究中进行评估。