Karan Dev, Wick Jo, Dubey Seema, Tawfik Ossama, Van Veldhuizen Peter
Department of Pathology, MCW Cancer Center and Prostate Cancer Center of Excellence, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI 53226, USA.
Department of Biostatistics and Data Science, University of Kansas Medical Center, Kansas City, KS 66160, USA.
Cancers (Basel). 2020 Oct 18;12(10):3033. doi: 10.3390/cancers12103033.
In this study, we investigated the potential of MIC-1 (macrophage inhibitory cytokine-1) on the severity of prostate cancer between African American men and Caucasians. Differences between the races were examined using Mann-Whitney tests for continuous variables and Fisher's exact tests for categorical variables. Pearson's correlation coefficient was used to identify associations between continuous measures across all samples and within each race. Analysis of variance, including clinical parameters, was used to identify differences in serum and urine MIC-1 levels between races. We found significant differences between the two races for age ( = 0.01), Gleason scores ( = 0.01), and stage of disease ( = 0.03). African American men in the study had higher Gleason scores (mean = 6.9) than Caucasians (mean = 6.5), during earlier stages of the disease. In Caucasian men with prostate cancer, serum MIC-1 expression was positively associated with age ( = 0.7, < 0.01). However, African American men had highly expressed MIC-1 and high Gleason scores ( = 0.16, = 0.3). Interestingly, the urine MIC-1 level was significantly higher in African American men with prostate cancer than in Caucasian patients. It appeared to be more sensitive and specific for African Americans (AUC = 0.85 vs. 0.56). Thus, high circulatory MIC-1 in prostate cancer patients may indicate MIC-1 as a potential biomarker to improve the diagnostic ability of an aggressive stage of prostate cancer in African American men. However, a larger cohort of sample analysis is required to validate these observations.
在本研究中,我们调查了巨噬细胞抑制细胞因子-1(MIC-1)在非裔美国男性和白种人前列腺癌严重程度方面的作用。对于连续变量,使用曼-惠特尼检验来检查种族之间的差异;对于分类变量,则使用费舍尔精确检验。皮尔逊相关系数用于确定所有样本以及每个种族内连续测量值之间的关联。方差分析(包括临床参数)用于确定种族之间血清和尿液中MIC-1水平的差异。我们发现两个种族在年龄(P = 0.01)、 Gleason评分(P = 0.01)和疾病分期(P = 0.03)方面存在显著差异。在疾病的早期阶段,本研究中的非裔美国男性的Gleason评分(平均 = 6.9)高于白种人(平均 = 6.5)。在患有前列腺癌的白种男性中,血清MIC-1表达与年龄呈正相关(r = 0.7,P < 0.01)。然而,非裔美国男性的MIC-1表达较高且Gleason评分也较高(r = 0.16,P = 0.3)。有趣的是,患有前列腺癌的非裔美国男性的尿液MIC-1水平显著高于白种患者。它对非裔美国人似乎更敏感且更具特异性(曲线下面积 = 0.85对0.56)。因此,前列腺癌患者中循环MIC-1水平较高可能表明MIC-1作为一种潜在的生物标志物,可提高对非裔美国男性侵袭性前列腺癌阶段的诊断能力。然而,需要更大规模的样本分析队列来验证这些观察结果。