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长链非编码 RNA OIP5-AS1 通过 miR-150-5p/PDCD4 轴在小儿重症社区获得性肺炎血液中的临床意义及潜在调控机制。

The Clinical Significance and the Potential Regulatory Mechanism of the LncRNA OIP5-AS1 in Paediatric Severe Community-Acquired Pneumonia Blood Through the MiR-150-5p/PDCD4 Axis.

机构信息

Department of Pediatrics, Xingtai People's Hospital, Xingtai, Hebei, China.

出版信息

Immunol Invest. 2024 May;53(4):541-558. doi: 10.1080/08820139.2024.2309557. Epub 2024 Jan 31.

Abstract

BACKGROUND

This study aimed to elucidate the clinical significance and regulatory mechanism of the long non-coding RNA OIP5-AS1 in severe community-acquired pneumonia (SCAP) among paediatric patients.

METHODS

qRT-PCR was used to assess the mRNA levels of OIP5-AS1. ROC curve analysis was used to assess the diagnostic significance of OIP5-AS1. Short-term prognostic significance was evaluated through Kaplan-Meier survival. An in vitro cell model was developed using LPS-induced MRC-5 cells. CCK-8, flow cytometry, and ELISA were conducted to measure cell viability, apoptosis, and inflammatory factor levels. The association between miR-150-5p and PDCD4 was confirmed through DLR assays.

RESULTS

Elevated OIP5-AS1 were observed in paediatric patients with SCAP, which enabled effective differentiation from healthy individuals. High expression of OIP5-AS1 correlated with reduced survival rates. OIP5-AS1 knockdown attenuated cell viability suppression and the promotion of apoptosis and inflammatory factors induced by LPS. However, this attenuation was reversed by reduced levels of miR-150-5p. miR-150-5p was identified as a target of PDCD4 and OIP5-AS1.

CONCLUSION

Increased OIP5-AS1 levels show potential as a valuable diagnostic and prognostic biomarker for paediatric patients with SCAP. This study illustrates its role in regulating cell viability, apoptosis, and the inflammatory response via the miR-150-5p/PDCD4 axis, acting as a ceRNA.

摘要

背景

本研究旨在阐明长链非编码 RNA OIP5-AS1 在儿科重症社区获得性肺炎(SCAP)中的临床意义和调控机制。

方法

采用 qRT-PCR 检测 OIP5-AS1 的 mRNA 水平。ROC 曲线分析评估 OIP5-AS1 的诊断意义。通过 Kaplan-Meier 生存分析评估短期预后意义。采用 LPS 诱导的 MRC-5 细胞建立体外细胞模型。CCK-8、流式细胞术和 ELISA 检测细胞活力、凋亡和炎症因子水平。通过 DLR 测定证实 miR-150-5p 与 PDCD4 的关联。

结果

在 SCAP 患儿中观察到 OIP5-AS1 水平升高,可有效区分健康个体。OIP5-AS1 高表达与生存率降低相关。OIP5-AS1 敲低可减轻 LPS 诱导的细胞活力抑制、促进细胞凋亡和炎症因子的产生。然而,miR-150-5p 水平降低可逆转这种抑制作用。miR-150-5p 被鉴定为 PDCD4 和 OIP5-AS1 的靶标。

结论

OIP5-AS1 水平升高可能成为 SCAP 患儿有价值的诊断和预后生物标志物。本研究表明其通过 miR-150-5p/PDCD4 轴调节细胞活力、凋亡和炎症反应,作为 ceRNA 发挥作用。

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