Cited by 24MicroRNA in disease regulationSepsis Diagnosis and TreatmentRespiratory Support and Mechanisms

miRNA-23a has effects to improve lung injury induced by sepsis in vitro and vivo study

Yang, Jing, Mao, Min, Zhen, Yuan-yuan·2018·Biomedicine & Pharmacotherapy

Abstract

Aim The aim of this study is to explain the effects and mechanism of miRNA-23a in lung injury which were induced by sepsis in vitro and vivo. Methods In the vitro study, The BEAS-2B cells were divided into 4 groups: NC, MC, miRNA and miRNA + PTEN agonist groups. The cell proliferation and apoptosis of difference groups were measured by MTT and flow cytometry, the relative proteins expression of difference groups were measured by WB assay. In the vivo study, the rats were also divided into 4 groups: NC, MC, miRNA and miRNA + PTEN agonist groups. The miRNA-23a expression of difference groups were evaluated by ISH in lung tissues of rats. The cell apoptosis of difference groups were evaluated by TUNEL assay in lung tissues; the relative proteins expression of difference groups were evaluated by IHC assay. Results Compared with NC group, the cell apoptosis rate of MC groups were significantly increased in vitro and vivo studies (P < 0.05, respectively). The relative proteins (PTEN, PI3K, AKT and P53) expressions of MC group were significantly differences (P < 0.05, respectively) compared with those of NC groups in vitro and vivo studies. However, with miRNA-23a infection, the cell apoptosis of miRNA group were significantly suppressed compared with MC groups, and the relative proteins (PTEN, PI3K, AKT and P53) of miRNA group were also significantly differences compared with MC groups in vitro and vivo studies (P < 0.05, respectively). Conclusion The miRNA-23a has improved lung in…

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Crossref · 10.1016/j.biopha.2018.07.097

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  • miR-23a can improve sepsis-induced lung injury through the PTEN/PI3K/AKT/P53 pathway.

    “Functional studies both in vivo and in vitro have implied that miR-23a can also improve sepsis-induced lung injury through the PTEN/PI3K/AKT/P53 pathway [36].”

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References 27 · Cited by 24

Authors
Yang, J., Mao, M., & Zhen, Y.-Y.
Affiliations
Qilu Hospital of Shandong University (CN)
Corresponding author
Yang, Jing
Venue
Biomedicine & Pharmacotherapy
Publisher
Elsevier BV
Published
2018-11
Volume
107
Pages
81-89
ISSN
0753-3322 (ISSN-L)
OpenAlex
W2887589341
Cited by
24
References
27
Citations by year
2025: 2 · 2024: 3 · 2023: 2 · 2022: 4 · 2021: 8 · 2020: 2 · 2019: 3
FWCI
0.98
Type
journal article
Language
en
Open access
closed
Locations
  • Biomedicine & Pharmacotherapy (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › MicroRNA in disease regulation
  • Health Sciences › Medicine › Epidemiology › Sepsis Diagnosis and Treatment
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Respiratory Support and Mechanisms
Keywords
sepsis-induced lung injury, PTEN, PI3K/Akt signaling, p53, apoptosis, BEAS-2B cells, miRNA-based therapy
MeSH terms
Animals, Cell Cycle, Cell Line, Humans, Male, Tumor Suppressor Protein p53, Rats, Wistar, Apoptosis, Sepsis, Phosphatidylinositol 3-Kinases, MicroRNAs, Cell Proliferation, Proto-Oncogene Proteins c-akt, Lung Injury

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