Chen Danze, Hao Shijia, Xu Jianzhen
Computational Systems Biology Lab, Shantou University Medical College (SUMC), Shantou, China.
Guangdong Provincial Key Laboratory for Diagnosis and Treatment of Breast Cancer, Shantou University Medical College (SUMC), Shantou, China.
Front Cell Dev Biol. 2021 Mar 11;9:647197. doi: 10.3389/fcell.2021.647197. eCollection 2021.
Increasing evidence indicates an association between the incidence of Alzheimer's disease (AD) and cancer development. Despite advances being made by comparisons from epidemiological studies, common pathways and molecular mechanisms, little is known about the identities of the circular RNAs (circRNAs) involved in the development and progression of these two pathologies and their possible correlations. The aim of this study was to explore the circRNA relationship between AD and cancer.
In this investigation, circRNAs that were significantly dysregulated in AD or associated with AD diagnosis, clinical dementia severity, and neuropathological severity, were examined in a large panel of 28 cancer types. On the basis of shared abnormal circRNAs in AD and cancers, we constructed a circRNA-micro RNA (miRNA)-messenger RNA (mRNA) network by leveraging experimentally identified miRNA-circRNA and miRNA-mRNA interactions from crosslinking-immunoprecipitation sequencing data.
An inverse correlation of expression pattern was found in acute myeloid leukemia, juvenile myelomonocytic leukemia, renal cell carcinoma, and myelofibrosis. CircRNAs associated with AD diagnosis and clinical severity demonstrated negative correlation in more cancer types. Notably, differentially expressed candidate circRNAs in temporal lobe epilepsy were not associated with any cancers. Gene Ontology and KEGG pathway analysis suggested the circRNA-regulated genes are significantly associated with interleukin-12-mediated signaling and viral response. CircPICALM, circRTN4 and circMAN2A1 are the hub nodes in the circRNA-miRNA-target network.
Our results indicated the relevance of inflammation signaling as a common pathogenesis shared by cancer and AD and provided novel insight for therapeutics targeting circRNAs.
越来越多的证据表明阿尔茨海默病(AD)的发病率与癌症发展之间存在关联。尽管通过流行病学研究、共同途径和分子机制的比较取得了进展,但对于参与这两种病理过程的发展和进展的环状RNA(circRNA)的身份及其可能的相关性知之甚少。本研究的目的是探索AD与癌症之间的circRNA关系。
在本研究中,在28种癌症类型的大样本中检测了在AD中显著失调或与AD诊断、临床痴呆严重程度和神经病理严重程度相关的circRNA。基于AD和癌症中共享的异常circRNA,我们利用交联免疫沉淀测序数据中实验确定的miRNA-circRNA和miRNA-mRNA相互作用构建了一个circRNA-微小RNA(miRNA)-信使RNA(mRNA)网络。
在急性髓系白血病、青少年粒单核细胞白血病、肾细胞癌和骨髓纤维化中发现了表达模式的负相关。与AD诊断和临床严重程度相关的circRNA在更多癌症类型中表现出负相关。值得注意的是,颞叶癫痫中差异表达的候选circRNA与任何癌症均无关联。基因本体论和KEGG通路分析表明,circRNA调控的基因与白细胞介素-12介导的信号传导和病毒反应显著相关。CircPICALM、circRTN4和circMAN2A1是circRNA-miRNA-靶标网络中的枢纽节点。
我们的结果表明炎症信号作为癌症和AD共同的发病机制具有相关性,并为靶向circRNA的治疗提供了新的见解。