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非裔美国人和白种人前列腺癌组织的表达差异表明,基质是侵袭性变化的部位。

Expression differences between African American and Caucasian prostate cancer tissue reveals that stroma is the site of aggressive changes.

机构信息

Department of Biology, San Diego State University, San Diego, CA.

出版信息

Int J Cancer. 2014 Jan 1;134(1):81-91. doi: 10.1002/ijc.28326. Epub 2013 Jul 13.

Abstract

In prostate cancer, race/ethnicity is the highest risk factor after adjusting for age. African Americans have more aggressive tumors at every clinical stage of the disease, resulting in poorer prognosis and increased mortality. A major barrier to identifying crucial gene activity differences is heterogeneity, including tissue composition variation intrinsic to the histology of prostate cancer. We hypothesized that differences in gene expression in specific tissue types would reveal mechanisms involved in the racial disparities of prostate cancer. We examined 17 pairs of arrays for AAs and Caucasians that were formed by closely matching the samples based on the known tissue type composition of the tumors. Using pair-wise t-test we found significantly altered gene expression between AAs and CAs. Independently, we performed multiple linear regression analyses to associate gene expression with race considering variation in percent tumor and stroma tissue. The majority of differentially expressed genes were associated with tumor-adjacent stroma rather than tumor tissue. Extracellular matrix, integrin family and signaling mediators of the epithelial-to-mesenchymal transition (EMT) pathways were all downregulated in stroma of AAs. Using MetaCore (GeneGo) analysis, we observed that 35% of significant (p < 10(-3)) pathways identified EMT and 25% identified immune response pathways especially for interleukins-2, -4, -5, -6, -7, -10, -13, -15 and -22 as the major changes. Our studies reveal that altered immune and EMT processes in tumor-adjacent stroma may be responsible for the aggressive nature of prostate cancer in AAs.

摘要

在前列腺癌中,种族/民族是调整年龄后的最高风险因素。非裔美国人在疾病的每个临床阶段都有更具侵袭性的肿瘤,导致预后较差和死亡率增加。确定关键基因活性差异的主要障碍是异质性,包括前列腺癌组织学固有的组织成分变化。我们假设特定组织类型中的基因表达差异将揭示与前列腺癌种族差异相关的机制。我们检查了 17 对来自非裔美国人和高加索人的数组,这些数组是通过根据肿瘤的已知组织类型组成密切匹配样本形成的。使用配对 t 检验,我们发现非裔美国人和高加索人之间的基因表达存在显著差异。独立地,我们进行了多元线性回归分析,考虑到肿瘤和基质组织的百分比变化,将基因表达与种族相关联。大多数差异表达的基因与肿瘤相邻的基质而不是肿瘤组织相关。细胞外基质、整合素家族和上皮间质转化 (EMT) 途径的信号转导介质在非裔美国人的基质中均下调。使用 MetaCore(GeneGo)分析,我们观察到 35%的显著(p < 10(-3))途径确定了 EMT,25%确定了免疫反应途径,特别是白细胞介素-2、-4、-5、-6、-7、-10、-13、-15 和 -22 作为主要变化。我们的研究表明,肿瘤相邻基质中改变的免疫和 EMT 过程可能是导致非裔美国人前列腺癌侵袭性的原因。

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