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长链非编码 RNA 结直肠肿瘤差异表达与哮喘患儿中的 miR-33a 和 miR-495 呈负相关,与炎症细胞因子呈正相关。

Long non-coding RNA colorectal neoplasia differentially expressed correlates negatively with miR-33a and miR-495 and positively with inflammatory cytokines in asthmatic children.

机构信息

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

出版信息

Clin Respir J. 2021 Nov;15(11):1175-1184. doi: 10.1111/crj.13424. Epub 2021 Aug 22.

Abstract

OBJECTIVES

It is reported that long non-coding RNA (lncRNA) colorectal neoplasia differentially expressed (CRNDE) targets microRNA (miR)-33a, miR-181a and miR-495 to regulate inflammation process, while few studies report their clinical application for paediatric asthma management. Therefore, this study aimed to explore the interaction of lncRNA CRNDE with miR-33a, miR-181a and miR-495, as well as their correlation with inflammation, exacerbation risk and severity in paediatric patients with asthma.

METHODS

Asthmatic exacerbation children (N = 65), asthmatic controlled children (N = 65) and controls (N = 65) were recruited. LncRNA CRNDE, miR-33a, miR-181a and miR-495 expressions in peripheral blood mononuclear cells were detected by RT-qPCR. Besides, serum inflammatory cytokines (including TNF-α, IL-1β, IL-6 and IL-17) were determined by enzyme-linked immunosorbent assay (ELISA).

RESULTS

LncRNA CRNDE, miR-33a and miR-495 expressions were different, while miR-181a expression was similar among asthmatic exacerbation children, asthmatic controlled children and controls. Moreover, lncRNA CRNDE negatively correlated with miR-33a and miR-495 in asthmatic exacerbation children and asthmatic controlled children, but not in controls. Further analyses showed that lncRNA CRNDE positively correlated with TNF-α, IL-1β, IL-17 and exacerbation severity, while it negatively correlated with FEV /FVC in asthmatic exacerbation children. Meanwhile, miR-33a, miR-181a and miR-495 all negatively correlated with some individual inflammatory cytokines, while only miR-33a negatively correlated with exacerbation severity in asthmatic exacerbation children.

CONCLUSION

LncRNA CRNDE correlates negatively with miR-33a and miR-495 and positively with inflammatory cytokines in asthmatic children.

摘要

目的

据报道,长链非编码 RNA(lncRNA)结直肠肿瘤差异表达(CRNDE)靶向 microRNA(miR)-33a、miR-181a 和 miR-495 来调节炎症过程,尽管很少有研究报告其在儿科哮喘管理中的临床应用。因此,本研究旨在探讨 lncRNA CRNDE 与 miR-33a、miR-181a 和 miR-495 的相互作用,以及它们与儿科哮喘患者炎症、加重风险和严重程度的相关性。

方法

招募哮喘加重儿童(N=65)、哮喘控制儿童(N=65)和对照者(N=65)。通过 RT-qPCR 检测外周血单个核细胞中 lncRNA CRNDE、miR-33a、miR-181a 和 miR-495 的表达。此外,通过酶联免疫吸附试验(ELISA)测定血清炎症细胞因子(包括 TNF-α、IL-1β、IL-6 和 IL-17)。

结果

lncRNA CRNDE、miR-33a 和 miR-495 的表达不同,而 miR-181a 的表达在哮喘加重儿童、哮喘控制儿童和对照者之间相似。此外,lncRNA CRNDE 在哮喘加重儿童和哮喘控制儿童中与 miR-33a 和 miR-495 呈负相关,但在对照者中无相关性。进一步分析显示,lncRNA CRNDE 与哮喘加重儿童的 TNF-α、IL-1β、IL-17 和加重严重程度呈正相关,而与 FEV/FVC 呈负相关。同时,miR-33a、miR-181a 和 miR-495 均与个别炎症细胞因子呈负相关,而仅 miR-33a 与哮喘加重儿童的加重严重程度呈负相关。

结论

lncRNA CRNDE 与哮喘儿童的 miR-33a 和 miR-495 呈负相关,与炎症细胞因子呈正相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c83/9291623/352afae4e7df/CRJ-15-1175-g003.jpg

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