Wang Jian, Yang Jing, Zou Ying, Huang Guo-Liang, He Zhi-Wei
Sino-American Cancer Research Institute, Key Laboratory for Medical Molecular Diagnostics of Guangdong Province, Guangdong Medical College, Dongguan, China.
Asian Pac J Cancer Prev. 2013;14(3):2023-8. doi: 10.7314/apjcp.2013.14.3.2023.
A number of studies have indicated that Nurr1, which belongs to a novel class of orphan nuclear receptors (the NR4A family), is important for carcinogenesis. Here we investigated expression of Nurr1 protein in benign and malignant human prostate tissues and association with clinicopathologic features using immunohistochemical techniques. Moreover, we also investigated the ability of Nurr1 to influence proliferation, migration, invasion and apoptosis of human prostate cancer cells using small interfering RNA silencing. Immunohistochemical analysis revealed that the expression of Nurr1 protein was higher in prostate cancer tissues than in benign prostate tissue (P < 0.001), levels being positively correlated with tumor T classification (P = 0.003), N classification (P = 0.017), M classification (P = 0.011) and the Gleason score (P = 0.020) of prostate cancer patients. In vitro, silencing of endogenous Nurr1 attenuated cell proliferation, migration and invasion, and induced apoptosis of prostate cancer cells. These results suggest that Nurr1 may be used as an indicator for prostate cancer progression and be useful for novel potential therapeutic strategies.
多项研究表明,属于一类新型孤儿核受体(NR4A家族)的Nurr1在致癌过程中起重要作用。在此,我们采用免疫组织化学技术研究了Nurr1蛋白在人前列腺良恶性组织中的表达情况及其与临床病理特征的相关性。此外,我们还利用小干扰RNA沉默技术研究了Nurr1影响人前列腺癌细胞增殖、迁移、侵袭和凋亡的能力。免疫组织化学分析显示,Nurr1蛋白在前列腺癌组织中的表达高于良性前列腺组织(P < 0.001),其表达水平与前列腺癌患者的肿瘤T分期(P = 0.003)、N分期(P = 0.017)、M分期(P = 0.011)及Gleason评分(P = 0.020)呈正相关。在体外,内源性Nurr1的沉默减弱了前列腺癌细胞的增殖、迁移和侵袭,并诱导了细胞凋亡。这些结果表明,Nurr1可能作为前列腺癌进展的一个指标,并且对新的潜在治疗策略具有重要意义。