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基于加权基因共表达网络分析的子宫内膜腺癌个体化医学中临床特征相关小 RNA 生物标志物的鉴定。

Identification of clinical trait-related small RNA biomarkers with weighted gene co-expression network analysis for personalized medicine in endocervical adenocarcinoma.

机构信息

Obstetrics and Gynecology Hospital, Fudan University, Shanghai 200011, China.

Shanghai Key Laboratory of Female Reproductive Endocrine Related Diseases, Institute of Metabolism and Integrative Biology, Institutes of Biomedical Sciences, Fudan University, Shanghai 200433, China.

出版信息

Aging (Albany NY). 2021 Sep 20;13(18):22361-22374. doi: 10.18632/aging.203543.

Abstract

Endocervical adenocarcinoma (EAC) is an aggressive type of endocervical cancer. At present, molecular research on EAC mainly focuses on the genome and mRNA transcriptome, the investigation of small RNAs in EAC has not been fully described. Here, we systematically explored small RNAs in 14 EAC patients with different subtypes using small RNA sequencing. MiRNAs and tRNA-derived RNAs (tDRs) accounted for the majority of mapped reads and the total number of miRNAs and tDRs maintained a relative balance. To explore the correlations between small RNAs expression and EAC with different clinical characteristics, we performed the weighted gene co-expression network analysis (WGCNA) and screened for hub small RNAs. From the key modules, we identified 9 small RNAs that were significantly related to clinical characteristics in EAC patients. Gene ontology and pathway analyses revealed that these molecules were involved in the pathogenesis of EAC. Our work provided new insights into EAC pathogenesis and successfully identified several small RNAs as candidate biomarkers for diagnosis and prognosis of EAC.

摘要

宫颈内膜腺癌(EAC)是一种侵袭性的宫颈内膜癌。目前,EAC 的分子研究主要集中在基因组和 mRNA 转录组上,对 EAC 中小 RNA 的研究尚未充分描述。在这里,我们使用小 RNA 测序系统地研究了 14 例具有不同亚型的 EAC 患者中的小 RNA。miRNAs 和 tRNA 衍生的 RNA(tDRs)占映射读数的大部分,miRNAs 和 tDRs 的总数保持相对平衡。为了探讨小 RNA 表达与不同临床特征的 EAC 之间的相关性,我们进行了加权基因共表达网络分析(WGCNA),并筛选出了枢纽小 RNA。从关键模块中,我们鉴定了 9 个与 EAC 患者临床特征显著相关的小 RNA。基因本体论和通路分析表明,这些分子参与了 EAC 的发病机制。我们的工作为 EAC 的发病机制提供了新的见解,并成功鉴定了几个小 RNA 作为 EAC 诊断和预后的候选生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d440/8507262/d2378a8edd8f/aging-13-203543-g001.jpg

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