Department of Medicine, Faculty of Medicine and Sciences of Health, University of Sherbrooke, Sherbrooke, Quebec, Canada.
Am J Pathol. 2013 Jul;183(1):266-76. doi: 10.1016/j.ajpath.2013.03.021. Epub 2013 May 13.
Colorectal cancer is the second leading cause of death from cancer. Osteopontin (OPN) is a component of tumor extracellular matrix identified as a key marker of cancer progression. The estrogen-related receptor α (ERRα) has been implicated in endocrine-related cancer development and progression, possibly through modulation of cellular energy metabolism. Previous reports that ERRα regulates OPN expression in bone prompted us to investigate whether ERRα controls OPN expression in human colorectal cancer. Using a tissue microarray containing 83 tumor-normal tissue pairs of colorectal cancer samples, we found that tumor epithelial cells displayed higher staining for ERRα than normal mucosa, in correlation with elevated OPN expression. In addition, knocking down endogenous ERRα led to reduced OPN expression in HT29 colon cancer cells. Promoter analysis, inhibition of ERRα activity, and expression and mutation of potential ERRα response elements in the proximal promoter of human OPN showed that ERRα and its obligate co-activator, peroxisome proliferator-activated receptor γ co-activator-1 α, positively control human OPN promoter activity. Furthermore, chromatin immunoprecipitation experiments confirmed in vivo occupancy of the OPN promoter by ERRα in HT29 cells, suggesting that OPN is a direct target of ERRα in colorectal cancer. These findings suggest an additional mechanism by which ERRα participates in the development and progression of colorectal cancer, further supporting the relevance of targeting ERRα with antagonists as anticancer agents.
结直肠癌是癌症死亡的第二大主要原因。骨桥蛋白 (OPN) 是肿瘤细胞外基质的组成部分,被确定为癌症进展的关键标志物。雌激素相关受体 α (ERRα) 与内分泌相关的癌症发展和进展有关,可能通过调节细胞能量代谢。先前的报告表明 ERRα 调节骨中的 OPN 表达,这促使我们研究 ERRα 是否控制人结直肠癌中的 OPN 表达。使用包含 83 对结直肠癌样本的肿瘤-正常组织的组织微阵列,我们发现肿瘤上皮细胞中 ERRα 的染色高于正常粘膜,与 OPN 表达升高相关。此外,敲低内源性 ERRα 导致 HT29 结肠癌细胞中的 OPN 表达减少。启动子分析、ERRα 活性抑制以及人 OPN 近端启动子中潜在 ERRα 反应元件的表达和突变表明,ERRα 和其必需的共激活剂过氧化物酶体增殖物激活受体 γ 共激活剂 1α 正向控制人 OPN 启动子活性。此外,染色质免疫沉淀实验证实 ERRα 在 HT29 细胞中体内占据 OPN 启动子,表明 OPN 是结直肠癌中 ERRα 的直接靶标。这些发现表明 ERRα 参与结直肠癌发生和发展的另一种机制,进一步支持用拮抗剂作为抗癌剂靶向 ERRα。