Erasmus MC Cancer Institute and Cancer Genomics Netherlands, University Medical Center Rotterdam, Department of Medical Oncology, 3015GD Rotterdam, the Netherlands.
Wellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, United Kingdom.
Genome Res. 2019 Mar;29(3):356-366. doi: 10.1101/gr.238121.118. Epub 2019 Jan 28.
Circular RNAs (circRNAs) are a class of RNAs that is under increasing scrutiny, although their functional roles are debated. We analyzed RNA-seq data of 348 primary breast cancers and developed a method to identify circRNAs that does not rely on unmapped reads or known splice junctions. We identified 95,843 circRNAs, of which 20,441 were found recurrently. Of the circRNAs that match exon boundaries of the same gene, 668 showed a poor or even negative ( < 0.2) correlation with the expression level of the linear gene. In silico analysis showed only a minority (8.5%) of circRNAs could be explained by known splicing events. Both these observations suggest that specific regulatory processes for circRNAs exist. We confirmed the presence of circRNAs of , , and in an independent pool of primary breast cancers. We identified circRNA profiles associated with subgroups of breast cancers and with biological and clinical features, such as amount of tumor lymphocytic infiltrate and proliferation index. siRNA-mediated knockdown of was shown to significantly reduce viability of the breast cancer cell lines MCF-7 and BT-474, further underlining the biological relevance of circRNAs. Furthermore, we found that circular, and not linear, levels are predictive for progression-free survival time to aromatase inhibitor (AI) therapy in advanced breast cancer patients, and found that is detectable in cell-free RNA from plasma. We showed that circRNAs are abundantly present, show characteristics of being specifically regulated, are associated with clinical and biological properties, and thus are relevant in breast cancer.
环状 RNA(circRNAs)是一类受到越来越多关注的 RNA,尽管它们的功能作用仍存在争议。我们分析了 348 例原发性乳腺癌的 RNA-seq 数据,并开发了一种不依赖未映射读数或已知剪接接头来识别 circRNAs 的方法。我们鉴定了 95843 个 circRNAs,其中 20441 个是反复出现的。在与同一基因外显子边界匹配的 circRNAs 中,有 668 个与线性基因的表达水平呈较差甚至负相关(<0.2)。计算机分析表明,只有少数(8.5%)circRNAs可以用已知的剪接事件来解释。这两种观察结果都表明,circRNAs 存在特定的调控过程。我们在独立的原发性乳腺癌样本中证实了 circRNAs 、 、和 的存在。我们鉴定了与乳腺癌亚组以及生物学和临床特征相关的 circRNA 谱,如肿瘤淋巴细胞浸润程度和增殖指数。siRNA 介导的 敲低显著降低了乳腺癌细胞系 MCF-7 和 BT-474 的活力,进一步强调了 circRNAs 的生物学相关性。此外,我们发现循环而非线性 水平可预测晚期乳腺癌患者接受芳香化酶抑制剂(AI)治疗的无进展生存时间,并且发现来自血浆的无细胞 RNA 中可检测到 。我们表明 circRNAs 大量存在,具有受特定调控的特征,与临床和生物学特性相关,因此在乳腺癌中具有相关性。