Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT 06520, USA.
Oncogene. 2010 Mar 18;29(11):1580-7. doi: 10.1038/onc.2009.445. Epub 2009 Dec 7.
MicroRNAs (miRNAs) have recently emerged as an important new class of cellular regulators that control various cellular processes and are implicated in human diseases, including cancer. Here, we show that loss of let-7 function enhances lung tumor formation in vivo, strongly supporting the hypothesis that let-7 is a tumor suppressor. Moreover, we report that exogenous delivery of let-7 to established tumors in mouse models of non-small-cell lung cancer (NSCLC) significantly reduces the tumor burden. These results demonstrate the therapeutic potential of let-7 in NSCLC and point to miRNA replacement therapy as a promising approach in cancer treatment.
微小 RNA(miRNAs)最近被认为是一类重要的细胞调控因子,它们可以调控各种细胞过程,并与人类疾病(包括癌症)有关。在这里,我们证明了 let-7 功能的丧失会增强体内肺肿瘤的形成,这有力地支持了 let-7 是一种肿瘤抑制因子的假说。此外,我们报告说,外源性给予非小细胞肺癌(NSCLC)小鼠模型中已建立的肿瘤 let-7,可显著降低肿瘤负担。这些结果表明 let-7 在 NSCLC 中的治疗潜力,并指出 miRNA 替代疗法是癌症治疗中一种很有前途的方法。