AC077690.1、AL049874.3和AP001037.1 lncrna在前列腺癌中的差异表达

Pub Date : 2022-01-01 DOI:10.2298/abs221025034l
Hexin Li, Xiaokun Tang, Gaoyuan Sun, Siyuan Xu, Luyao Wang, Lanxin Zhang, Ya-qun Zhang, Fei Su, Lili Zhang, Wei Zhang
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引用次数: 0

摘要

前列腺癌(PCa)是世界范围内常见的一种癌症。前列腺癌的发病率随着年龄的增长而增加,是男性最常见的恶性肿瘤。组织活检和血清前列腺特异性抗原仍是诊断疑似前列腺癌的标准。长链非编码RNA (lncRNA)通过招募转录调控因子来促进前列腺癌的进展。我们利用高通量测序数据和生物信息学分析鉴定了PCa中特异性表达的lncrna,并筛选出三个特异性lncrna进行进一步分析:AC077690.1, AL049874.3和AP001037.1。我们构建了一个lncRNA调控网络,并使用差异表达的mRNA相互作用来预测所选lncRNA的功能。对这三个lncrna的功能富集分析和PCR验证表明,它们与众所周知的PI3K-AktmTOR和参与PCa的叉头盒蛋白(FOXO)信号通路密切相关。通过了解这些分子和信号通路之间的相关相互作用,lncrna可能成为PCa治疗靶点的潜在候选者。
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Differentially expressed AC077690.1, AL049874.3 and AP001037.1 lncRNAs in prostate cancer
Prostate cancer (PCa) is a common type of cancer worldwide. The incidence of PCa increases with age and it is the most common malignant tumor in men. Tissue biopsy and the serum prostatespecific antigen are still the standards for diagnosing suspected PCa. Long non-coding RNA (lncRNA) contributes to the progression of PCa by recruiting transcriptional regulators. We utilized highthroughput sequencing data and bioinformatics analysis to identify specifically expressed lncRNAs in PCa and filtered out three specific lncRNAs for further analysis: AC077690.1, AL049874.3 and AP001037.1. We constructed a lncRNA regulatory network and used differentially expressed mRNA interactions to predict the functions of the selected lncRNAs. Functional enrichment analysis and PCR verification of these three lncRNAs revealed that they were closely related to well-known PI3K-AktmTOR and the forkhead box protein (FOXO) signaling pathways involved in PCa. By understanding the related interactions between these molecules and signaling pathways, the lncRNAs could be potential candidates for therapeutic targets in PCa.
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