Evidence map›Paper›PMID 33421511›Full record

ArticleGastroenterology2021

miR-10b-5p Rescues Diabetes and Gastrointestinal Dysmotility.

Rajan Singh, Se Eun Ha, Lai Wei, Byungchang Jin, Hannah Zogg, Sandra M Poudrier, Brian G Jorgensen, Chanjae Park, Charles F Ronkon, Allison Bartlett and 9 more

Open access · greenAbstract read
In one paragraph

Article in Gastroenterology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
7.3field-weighted citation impact, top 2% 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

55 citing papers in PubMed, 81 citations in OpenAlex.

  1. Article
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  18. miR-10a/b-5p-NCOR2 Regulates Insulin-Resistant Diabetes in Female Mice.International journal of molecular sciences · 2024
    Article
  19. MicroRNAs in diabetic macroangiopathy.Cardiovascular diabetology · 2024
    Review
  20. Oligonucleotide therapies for nonalcoholic steatohepatitis.Molecular therapy. Nucleic acids · 2024
    Review
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

19 authors at 3 institutions in 2 countries.

Rajan SinghDepartment of Physiology and Cell Biology, School of Medicine, University of Nevada, Reno, Nevada.
Se Eun HaDepartment of Physiology and Cell Biology, School of Medicine, University of Nevada, Reno, Nevada.
Lai WeiDepartment of Physiology and Cell Biology, School of Medicine, University of Nevada, Reno, Nevada.
Byungchang JinDepartment of Physiology and Cell Biology, School of Medicine, University of Nevada, Reno, Nevada.
Hannah ZoggDepartment of Physiology and Cell Biology, School of Medicine, University of Nevada, Reno, Nevada.
Sandra M PoudrierDepartment of Physiology and Cell Biology, School of Medicine, University of Nevada, Reno, Nevada.
Brian G JorgensenDepartment of Physiology and Cell Biology, School of Medicine, University of Nevada, Reno, Nevada.
Chanjae ParkDepartment of Physiology and Cell Biology, School of Medicine, University of Nevada, Reno, Nevada.
Charles F RonkonDepartment of Physiology and Cell Biology, School of Medicine, University of Nevada, Reno, Nevada.
Allison BartlettDepartment of Physiology and Cell Biology, School of Medicine, University of Nevada, Reno, Nevada.
Sung ChoDepartment of Physiology and Cell Biology, School of Medicine, University of Nevada, Reno, Nevada.
Addison MoralesDepartment of Physiology and Cell Biology, School of Medicine, University of Nevada, Reno, Nevada.
Yu Heon ChungDivision of Biological Sciences, Wonkwang University, Iksan, Chonbuk, Korea.
Moon Young LeeDepartment of Physiology and Cell Biology, School of Medicine, University of Nevada, Reno, Nevada; Department of Physiology, Wonkwang Digestive Disease Research Institute and Institute of Wonkwang Medical Science, School of Medicine, Wonkwang University, Iksan, Chonbuk, Korea.
Jong Kun ParkDivision of Biological Sciences, Wonkwang University, Iksan, Chonbuk, Korea.
Andrés Gottfried-BlackmoreDivision of Gastroenterology and Hepatology, Stanford University School of Medicine, Stanford, California.
Linda NguyenDivision of Gastroenterology and Hepatology, Stanford University School of Medicine, Stanford, California.
Kenton M SandersDepartment of Physiology and Cell Biology, School of Medicine, University of Nevada, Reno, Nevada.
Seungil RoDepartment of Physiology and Cell Biology, School of Medicine, University of Nevada, Reno, Nevada. Electronic address: sro@med.unr.edu.
University of Nevada, Reno · USStanford University · USWonkwang University · KR

Funding

Tissue, Cell and Tissue Culture CoreP01DK041315 · NIDDK · UNIVERSITY OF NEVADA RENO · PI SANDERS, KENTON M · 1989 to 2018
$26.3M
Single Cell Molecular ExpressionP30GM110767 · NIGMS · UNIVERSITY OF NEVADA RENO · PI SANDERS, KENTON M · 2014 to 2018
$5.4M
Stanford TRANSFORM I2T ProgramR25AI147369 · NIAID · STANFORD UNIVERSITY · PI CHERTOW, GLENN MATTHEW, SINGH, UPINDER · 2019 to 2023
$1.8M
Roles of DNA methylation in gastrointestinal smooth muscle cellsR01DK094886 · NIDDK · UNIVERSITY OF NEVADA RENO · PI RO, SEUNGIL · 2012 to 2016
$1.5M
Engineering of functional smooth muscle cells from gastrointestinal myofibroblastR01DK103055 · NIDDK · UNIVERSITY OF NEVADA RENO · PI RO, SEUNGIL · 2015 to 2018
$1.3M
microRNAs targeting Kit inhibit the development and maintenance of ICCR21DK091725 · NIDDK · UNIVERSITY OF NEVADA RENO · PI RO, SEUNGIL · 2011 to 2012
$388k
NIAID NIH HHS R25 AI147369NIDDK NIH HHS P01 DK041315NIDDK NIH HHS R01 DK094886NIDDK NIH HHS R01 DK103055NIDDK NIH HHS R21 DK091725NIGMS NIH HHS P30 GM110767
6 · The paper itself

Abstract

BACKGROUND &

aimsInterstitial cells of Cajal (ICCs) and pancreatic β cells require receptor tyrosine kinase (KIT) to develop and function properly. Degeneration of ICCs is linked to diabetic gastroparesis. The mechanisms linking diabetes and gastroparesis are unclear, but may involve microRNA (miRNA)-mediated post-transcriptional gene silencing in KIT

methodsWe performed miRNA-sequencing analysis from isolated ICCs in diabetic mice and plasma from patients with idiopathic and diabetic gastroparesis. miR-10b-5p target genes were identified and validated in mouse and human cell lines. For loss-of-function studies, we used KIT

resultsmiR-10b-5p is highly expressed in ICCs from healthy mice, but drastically depleted in ICCs from diabetic mice. A conditional knockout of mir-10b in KIT

conclusionsmiR-10b-5p is a key regulator in diabetes and gastrointestinal dysmotility via the KLF11-KIT pathway. Restoration of miR-10b-5p may provide therapeutic benefits for these disorders.

Indexed as

Gastric EmptyingGastrointestinal TransitAdultAgedAnimalsApoptosis Regulatory ProteinsBlood GlucoseDiabetes MellitusDisease Models, AnimalFemaleGastroparesisHEK293 CellsHumansInsulin-Secreting CellsInterstitial Cells of CajalMaleApoptosis Regulatory ProteinsBlood GlucoseKIT protein, humanKit protein, mouseKLF11 protein, humanKLF11 protein, mouseMicroRNAsMIRN10 microRNA, humanMIRN10 microRNA, mouseProto-Oncogene Proteins c-kitRepressor ProteinsDiabetic GastroparesisGastrointestinal DysmotilityInterstitial Cells of CajalMicroRNAsPancreatic β Cells

Identifiers

PMID33421511
PMCPMC8532043
OpenAlexW3120915673

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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 Socratic graph.