Lu Lingeng, Katsaros Dionyssios, Shaverdashvili Khvaramze, Qian Biyun, Wu Yixing, de la Longrais Irene A Rigault, Preti Mario, Menato Guido, Yu Herbert
Department of Epidemiology and Public Health, Yale Cancer Center, Yale University School of Medicine, 60 College Street, New Haven, CT 06520-8034, USA.
Eur J Cancer. 2009 Aug;45(12):2212-8. doi: 10.1016/j.ejca.2009.05.003. Epub 2009 May 26.
Lin-28 and lin-28B are RNA-binding proteins which can block microRNA let-7 maturation and affect the differentiation and proliferation of embryonic stem cells. Lin-28 may also regulate the expression of insulin-like growth factor II (IGF-II). As one of the pluripotent factors involved in making induced pluripotent stem cells (iPS), lin-28 is considered a potential therapeutic target for cancer treatment. To further understand the role of lin-28 in cancer, we analysed the expression of lin-28 and its homologue lin-28B in tumour samples, and evaluated their associations with let-7a maturation, IGF-II expression, disease features and outcomes in 211 patients with primary epithelial ovarian cancer. The analysis showed that both lin-28 and lin-28B were positively correlated with primary and pre-let-7a-3; lin-28B, not lin-28, was inversely correlated with mature let-7a. A positive correlation was also observed between lin-28B and IGF-II expression, while no association was found between lin-28B and IGF-I or IGFBP-3. The study further demonstrated that lin-28B expression was associated with the risk of disease progression and death; patients with high lin-28B had shorter progression-free and overall survival than those with low lin-28B. These results seem to support the findings of recent in vitro experiments, showing that lin-28 blocks the process of let-7a maturation. Our study also suggests that lin-28B may promote ovarian cancer progression and serve as an unfavourable prognostic marker for the disease. The correlation between lin-28B and IGF-II indicates that the growth factor may mediate the effect of lin-28B on tumour growth.
Lin-28和lin-28B是RNA结合蛋白,它们可以阻断微小RNA let-7的成熟,并影响胚胎干细胞的分化和增殖。Lin-28也可能调节胰岛素样生长因子II(IGF-II)的表达。作为参与诱导多能干细胞(iPS)形成的多能因子之一,lin-28被认为是癌症治疗的潜在靶点。为了进一步了解lin-28在癌症中的作用,我们分析了lin-28及其同源物lin-28B在肿瘤样本中的表达,并评估了它们与211例原发性上皮性卵巢癌患者中let-7a成熟、IGF-II表达、疾病特征及预后的相关性。分析表明,lin-28和lin-28B均与初级和前体let-7a-3呈正相关;与lin-28不同,lin-28B与成熟let-7a呈负相关。lin-28B与IGF-II表达之间也存在正相关,而lin-28B与IGF-I或IGFBP-3之间未发现相关性。该研究进一步证明,lin-28B的表达与疾病进展和死亡风险相关;lin-28B高表达的患者无进展生存期和总生存期均短于lin-28B低表达的患者。这些结果似乎支持了最近的体外实验结果,表明lin-28阻断了let-7a的成熟过程。我们的研究还表明,lin-28B可能促进卵巢癌进展,并可作为该疾病的不良预后标志物。lin-28B与IGF-II之间的相关性表明,生长因子可能介导lin-28B对肿瘤生长的影响。