Fernandez Nicolas, Chavarriaga Julian, Ayala Paola, Pedraza Adriana, Bolivar John, Prada Juan Guillermo, Cataño Juan Guillermo, García-Perdomo Herney Andres, Villanueva Juliana, Varela Daniela, Zarante Ignacio
Division of Urology Seattle Children's Hospital, University of Washington, Seattle, WA, USA.
Division of Urology, Clínica Imbanaco - Quiron Salud, Cali, Colombia.
Res Rep Urol. 2022 Mar 1;14:63-70. doi: 10.2147/RRU.S332578. eCollection 2022.
To identify micro-RNAs (miRNAs) expression profiles in peripheral blood plasma that could play a role as potential biomarkers in patients who progressed to castration-resistant prostate cancer (CRPC). Liquid biopsy analysis of miRNAs is a fast-developing field with a considerable likelihood to predict tumor progression and metastasis by targeting genes involved in oncogenesis.
Differential expression analysis of miRNAs profile in CRPC patients was performed by creating small RNA libraries of circulating miRNAs using HiSeq2500 Illumina platform. A secondary analysis of aligned reads with miRNA identification and quantification was performed using miARmaSeq. Using the Bowtie algorithm, the selected variants were compared to reference nucleotide sequence GRCh38 and miRbase. Novel miRNA sequences were structurally analyzed using mirDeep2.
A total of 16 patients with CRPC were included for analysis. Identified circulating miRNAs were hsa-miR-885-3p, hsa-miR-4467, hsa-miR-4686, hsa-miR-146a-3p, hsa-miR-6514-5p. Genes identified as regulated by these miRNAs were , and .
We explored the miRNA expression profile in patients with CRPC, identifying five miRNAs implicated in the regulation of genes involved in prostate cancer (PCa) oncogenesis and progression. We also found miRNA 855-3p in peripheral blood for the first time, which has a critical role in tumor growth mechanisms and higher expression profile than in healthy individuals.
确定外周血血浆中的微小RNA(miRNA)表达谱,这些miRNA可能作为去势抵抗性前列腺癌(CRPC)进展患者的潜在生物标志物。对miRNA进行液体活检分析是一个快速发展的领域,极有可能通过靶向参与肿瘤发生的基因来预测肿瘤进展和转移。
利用Illumina HiSeq2500平台创建循环miRNA的小RNA文库,对CRPC患者的miRNA谱进行差异表达分析。使用miARmaSeq对与miRNA鉴定和定量的比对读数进行二次分析。使用Bowtie算法,将选定的变体与参考核苷酸序列GRCh38和miRbase进行比较。使用mirDeep2对新的miRNA序列进行结构分析。
共纳入16例CRPC患者进行分析。鉴定出的循环miRNA为hsa-miR-885-3p、hsa-miR-4467、hsa-miR-4686、hsa-miR-146a-3p、hsa-miR-6514-5p。被这些miRNA调控的基因分别为 、 和 。
我们探索了CRPC患者的miRNA表达谱,鉴定出5种与前列腺癌(PCa)发生和进展相关基因调控有关的miRNA。我们还首次在外周血中发现了miRNA 855-3p,它在肿瘤生长机制中起关键作用,且表达谱高于健康个体。