Evidence map›Paper›PMID 33299380›Full record

ArticleMediators of inflammation2020

Total Glucosides of Paeony Alleviate Cell Apoptosis and Inflammation by Targeting the Long Noncoding RNA XIST/MicroRNA-124-3p/ITGB1 Axis in Renal Ischemia/Reperfusion Injury.

Fang Chen, Yi Hu, Yuetao Xie, Zonghui Zhao, Lin Ma, Zhili Li, Wanlong Tan

Open access · goldAbstract read
In one paragraph

Article in Mediators of inflammation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.4field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 33 citations in OpenAlex.

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  15. Non-Coding RNAs in Kidney Diseases: The Long and Short of Them.International journal of molecular sciences · 2021
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Fang ChenDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong 510515, China.ORCID https://orcid.org/0000-0002-7681-6917
Yi HuDepartment of Anesthesiology, Shenzhen Children's Hospital, Shenzhen, Guangdong 518038, China.ORCID https://orcid.org/0000-0003-0643-5825
Yuetao XieDepartment of Anesthesiology, Shenzhen Children's Hospital, Shenzhen, Guangdong 518038, China.ORCID https://orcid.org/0000-0002-7773-6919
Zonghui ZhaoDepartment of Anesthesiology, Shenzhen Children's Hospital, Shenzhen, Guangdong 518038, China.ORCID https://orcid.org/0000-0002-6721-6223
Lin MaDepartment of Anesthesiology, Shenzhen Children's Hospital, Shenzhen, Guangdong 518038, China.ORCID https://orcid.org/0000-0001-6745-2990
Zhili LiDepartment of Anesthesiology, Shenzhen Children's Hospital, Shenzhen, Guangdong 518038, China.ORCID https://orcid.org/0000-0002-8583-0112
Wanlong TanDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong 510515, China.ORCID https://orcid.org/0000-0001-6732-3267
Shenzhen Children's Hospital · CNNanfang Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveRenal ischemia/reperfusion injury (RI/RI) is the main cause of acute kidney injury. Total glucosides of paeony (TGP) are a traditional Chinese medicine. This study was aimed at exploring the role of TGP in RI/RI and its underlying mechanism of action.

methodsRat RI/RI models were constructed by surgical operation. Serum creatinine (Scr) and blood urea nitrogen (BUN) were used to evaluate renal function. The levels of proinflammatory cytokines were detected by ELISA. RI/RI was simulated by hypoxia/reoxygenation (H/R) treatment in renal cells

resultsTGP improved renal function and inhibited inflammatory responses after RI/RI. XIST expression was highly expressed in rat RI/RI models and H/R-treated renal cells, whereas treatment with TGP downregulated the XIST expression. Additionally, TGP increased viability and attenuated apoptosis and inflammation of H/R-treated renal cells via inhibiting XIST. Moreover, XIST was competitively bound to miR-124-3p, and ITGB1 was a target of miR-124-3p. miR-124-3p overexpression or ITGB1 inhibition rescued the reduction effect on viability and mitigated the promoting effects on cell apoptosis and inflammation caused by XIST overexpression in H/R-treated renal cells.

conclusions

Indexed as

ApoptosisAcute Kidney InjuryAnimalsBlood Urea NitrogenCell ProliferationCell SurvivalCreatinineDrugs, Chinese HerbalEpithelial CellsGlucosidesInflammationIntegrin beta1KidneyMaleMedicine, Chinese TraditionalMicroRNAsCreatinineDrugs, Chinese HerbalGlucosidesIntegrin beta1MicroRNAsMIRN124 microRNA, ratRNA, Long NoncodingXIST non-coding RNA

Identifiers

PMID33299380
PMCPMC7710434
OpenAlexW3107885730

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.