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A miRNA's insight into the regenerating heart: a concise descriptive analysis

机译:MiRNA对再生心脏的洞察力:简明的描述性分析

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摘要

Manipulation of microRNA (miRNA) expression has been shown to induce cardiac regeneration, consolidating their therapeutic potential. However, studies often validate only a few miRNA targets in each experiment and hold these targets entirely accountable for the miRNAs' action, ignoring the other potential molecular and cellular events involved. In this report, experimentally validated miRNAs are used as a window of discovery for the possible genes and signaling pathways that are implicated in cardiac regeneration. A thorough evidence search was conducted, and identified miRNAs were submitted for in silico dissection using reliable bioinformatics tools. A total of 46 miRNAs were retrieved from existing literature. Shared targets between miRNAs included well-recognized genes such as BCL-2, CCND1, and PTEN. Transcription factors that are possibly involved in the regeneration process such as SP1, CTCF, and ZNF263 were also identified. The analysis confirmed well-established signaling pathways involved in cardiac regeneration such as Hippo, MAPK, and AKT signaling, and revealed new pathways such as ECM-receptor interaction, and FoxO signaling on top of hormonal pathways such as thyroid, adrenergic, and estrogen signaling pathways. Additionally, a set of differentially expressed miRNAs were identified as potential future experimental candidates.
机译:调控microRNA(miRNA)表达已被证明能诱导心脏再生,巩固其治疗潜力。然而,研究往往只验证了每个实验中的几个miRNA靶点,并认为这些靶点对miRNA的作用完全负责,而忽略了涉及的其他潜在分子和细胞事件。在本报告中,实验验证的miRNA被用作发现心脏再生相关基因和信号通路的窗口。进行了彻底的证据搜索,并使用可靠的生物信息学工具提交了已鉴定的miRNA进行电子解剖。从现有文献中共检索到46个miRNA。miRNA之间的共同靶点包括公认的基因,如BCL-2、CCND1和PTEN。还发现了可能参与再生过程的转录因子,如SP1、CTCF和ZNF263。该分析证实了参与心脏再生的成熟信号通路,如Hippo、MAPK和AKT信号,并揭示了新的途径,如ECM受体相互作用和FoxO信号,以及激素途径,如甲状腺、肾上腺素和雌激素信号途径。此外,一组差异表达的miRNA被确定为未来潜在的实验候选基因。

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