Huang Chen-Tsung, Oyang Yen-Jen, Huang Hsuan-Cheng, Juan Hsueh-Fen
Graduate Institute of Biomedical Electronics and Bioinformatics, National Taiwan University, Taipei, Taiwan.
Institute of Biomedical Informatics and Center for Systems and Synthetic Biology, National Yang-Ming University, Taipei, Taiwan.
Sci Rep. 2014 Sep 29;4:6495. doi: 10.1038/srep06495.
Papillary thyroid carcinoma (PTC) is a common endocrine malignancy with low death rate but increased incidence and recurrence in recent years. MicroRNAs (miRNAs) are small non-coding RNAs with diverse regulatory capacities in eukaryotes and have been frequently implied in human cancer. Despite current progress, however, a panoramic overview concerning miRNA regulatory networks in PTC is still lacking. Here, we analyzed the expression datasets of PTC from The Cancer Genome Atlas (TCGA) Data Portal and demonstrate for the first time that immune responses are significantly enriched and under specific regulation in the direct miRNA--target network among distinctive PTC variants to different extents. Additionally, considering the unconventional properties of miRNAs, we explore the protein-coding competing endogenous RNA (ceRNA) and the modulatory networks in PTC and unexpectedly disclose concerted regulation of immune responses from these networks. Interestingly, miRNAs from these conventional and unconventional networks share general similarities and differences but tend to be disparate as regulatory activities increase, coordinately tuning the immune responses that in part account for PTC tumor biology. Together, our systematic results uncover the intensive regulation of immune responses underlain by miRNA-mediated networks in PTC, opening up new avenues in the management of thyroid cancer.
甲状腺乳头状癌(PTC)是一种常见的内分泌恶性肿瘤,死亡率较低,但近年来发病率和复发率有所上升。微小RNA(miRNA)是真核生物中具有多种调控能力的小型非编码RNA,经常与人类癌症相关。然而,尽管目前取得了进展,但仍缺乏关于PTC中miRNA调控网络的全景概述。在这里,我们分析了来自癌症基因组图谱(TCGA)数据门户的PTC表达数据集,并首次证明在不同程度的独特PTC变体之间的直接miRNA-靶标网络中,免疫反应显著富集且受到特定调控。此外,考虑到miRNA的非常规特性,我们探索了PTC中的蛋白质编码竞争性内源RNA(ceRNA)和调控网络,并意外地揭示了这些网络对免疫反应的协同调控。有趣的是,来自这些常规和非常规网络的miRNA具有一般的相似性和差异,但随着调控活性的增加往往会有所不同,共同协调免疫反应,这在一定程度上解释了PTC的肿瘤生物学特性。总之,我们的系统结果揭示了PTC中miRNA介导的网络对免疫反应的密集调控,为甲状腺癌的治疗开辟了新途径。