Evidence map›Paper›PMID 34295698›Full record

ArticleCardiovascular diagnosis and therapy2021

LncRNA XIST serves as a diagnostic biomarker in gestational diabetes mellitus and its regulatory effect on trophoblast cell via miR-497-5p/FOXO1 axis.

Yanchuan Li, Xiaohua Yuan, Ziyun Shi, Haili Wang, Duomei Ren, Ya Zhang, Yangyang Fan, Yanfeng Liu, Zhangxia Cui

Open access · diamondAbstract read
In one paragraph

Article in Cardiovascular diagnosis and therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

18 citing papers in PubMed, 30 citations in OpenAlex.

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  17. Knockdown of lncRNA XIST Ameliorates IL-1Cardiovascular therapeutics · 2022
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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

9 authors at 5 institutions in 1 country.

Yanchuan LiDepartment of Obstetrics, Shaanxi Provincial People's Hospital, Xi'an, China.
Xiaohua YuanDepartment of Obstetrics and Gynecology, Shaanxi Provincial People's Hospital, Xi'an, China.
Ziyun ShiDepartment of Obstetrics, Shaanxi Provincial People's Hospital, Xi'an, China.
Haili WangDepartment of Obstetrics, Shaanxi Provincial People's Hospital, Xi'an, China.
Duomei RenDepartment of Obstetrics, Shaanxi Provincial People's Hospital, Xi'an, China.
Ya ZhangDepartment of Obstetrics, Shaanxi Provincial People's Hospital, Xi'an, China.
Yangyang FanDepartment of Obstetrics, Shaanxi Provincial People's Hospital, Xi'an, China.
Yanfeng LiuDepartment of General Surgery, The Second Affiliated Hospital, Xi'an Medical University, Xi'an, China.
Zhangxia CuiDepartment of Obstetrics, The Second Affiliated Hospital of Shaanxi University of Chinese Medicine (Xi Xian Central Hospital), Xianyang, China.
Shanxi Medical University · CNShaanxi Provincial People's Hospital · CNAffiliated Hospital of Shaanxi University of Chinese Medicine · CNShaanxi Provincial People's Hospital · CNXi'an Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGestational diabetes mellitus (GDM) is increasingly common in pregnancy. This study's purpose was to identify the expression of XIST and manifest the potential mechanism of XIST in GDM.

methodsNinety-three patients with GDM and 93 normal pregnant women were included in this investigation. qRT-PCR was conducted to evaluate the expression of miR-497-5p and XIST and the relationship between XIST and fasting blood glucose (FBG) was explored by Pearson assay. The clinical diagnosis of XIST on GDM patients was validated by the receiver operator characteristic (ROC) curve. Cell counting kit-8 (CCK-8) was applied to elucidate cell viability. Luciferase reporter assay was performed to document the relationship among XIST, miR-497-5p, and FOXO1.

resultsThe expression of XIST was increased in GDM patients and HTR-8/SVneo cell models caused by high glucose (HG). The expression of XIST was associated with the FBG levels and appeared to be a feasible indicator in discriminating GDM patients. The expression of miR-497-5p was prominently reduced in GDM patients and cell models. Inhibition of XIST might alleviate the adverse function of HG on cell viability via sponging miR-497-5p. FOXO1 was proved to be a downstream target gene of miR-497-5p.

conclusionsOverexpression of XIST and downregulation of miR-497-5p were indicated in this publication. XIST might serve as a promising diagnostic marker for GDM patients. XIST/miR-497-5p/FOXO1 axis played a critical role in the regulation of trophoblast cells.

Indexed as

cell viabilitydiagnosisgestational diabetes mellitus (GDM)XIST/miR-497-5p/FOXO1

Identifiers

PMID34295698
PMCPMC8261738
OpenAlexW3157079243

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.