Rider Jennifer R, Fiorentino Michelangelo, Kelly Rachel, Gerke Travis, Jordahl Kristina, Sinnott Jennifer A, Giovannucci Edward L, Loda Massimo, Mucci Lorelei A, Finn Stephen
Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA,
Pathology Unit, Addarii Institute of Oncology, S. Orsola-Malphighi Hospital, 40126 Bologna, Italy.
Carcinogenesis. 2015 Jun;36(6):639-47. doi: 10.1093/carcin/bgv048. Epub 2015 Apr 11.
To investigate the role of adiponectin receptor 2 (AdipoR2) in aggressive prostate cancer we used immunohistochemistry to characterize AdipoR2 protein expression in tumor tissue for 866 men with prostate cancer from the Physicians' Health Study and the Health Professionals Follow-up Study. AdipoR2 tumor expression was not associated with measures of obesity, pathological tumor stage or prostate-specific antigen (PSA) at diagnosis. However, AdipoR2 expression was positively associated with proliferation as measured by Ki-67 expression quartiles (P-trend < 0.0001), with expression of fatty acid synthase (P-trend = 0.001), and with two measures of angiogenesis (P-trend < 0.1). An inverse association was observed with apoptosis as assessed by the TUNEL assay (P-trend = 0.006). Using Cox proportional hazards regression and controlling for age at diagnosis, Gleason score, year of diagnosis category, cohort and baseline BMI, we identified a statistically significant trend for the association between quartile of AdipoR2 expression and lethal prostate cancer (P-trend = 0.02). The hazard ratio for lethal prostate cancer for the two highest quartiles, as compared to the two lowest quartiles, of AdipoR2 expression was 1.9 (95% confidence interval [CI]: 1.2-3.0). Results were similar when additionally controlling for categories of PSA at diagnosis and Ki-67 expression quartiles. These results strengthen the evidence for the role of AdipoR2 in prostate cancer progression.
为了研究脂联素受体2(AdipoR2)在侵袭性前列腺癌中的作用,我们采用免疫组织化学方法,对来自医师健康研究和卫生专业人员随访研究的866例前列腺癌男性患者肿瘤组织中的AdipoR2蛋白表达进行了特征分析。AdipoR2在肿瘤中的表达与肥胖指标、病理肿瘤分期或诊断时的前列腺特异性抗原(PSA)无关。然而,AdipoR2的表达与通过Ki-67表达四分位数测量的增殖呈正相关(P趋势<0.0001),与脂肪酸合酶的表达呈正相关(P趋势=0.001),并与两种血管生成指标呈正相关(P趋势<0.1)。通过TUNEL检测评估,发现其与细胞凋亡呈负相关(P趋势=0.006)。使用Cox比例风险回归并控制诊断时的年龄、Gleason评分、诊断年份类别、队列和基线BMI,我们发现AdipoR2表达四分位数与致命性前列腺癌之间的关联具有统计学意义的趋势(P趋势=0.02)。与AdipoR2表达最低的两个四分位数相比,最高的两个四分位数发生致命性前列腺癌 的风险比为1.9(95%置信区间[CI]:1.2 - 3.0)。在额外控制诊断时的PSA类别和Ki-67表达四分位数后,结果相似。这些结果进一步证明了AdipoR2在前列腺癌进展中的作用。