Evidence map›Paper›PMID 34571853›Full record

ReviewCells2021

Role of MicroRNA in Inflammatory Bowel Disease: Clinical Evidence and the Development of Preclinical Animal Models.

Kanika Suri, Jason A Bubier, Michael V Wiles, Leonard D Shultz, Mansoor M Amiji, Vishnu Hosur

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

22 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
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  15. miRNA Molecules-Late Breaking Treatment for Inflammatory Bowel Diseases?International journal of molecular sciences · 2023
    Review
  16. MicroRNAs in Inflammatory Bowel Disease and Its Complications.International journal of molecular sciences · 2022
    Review
  17. Review
  18. Review
  19. Review
  20. 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

6 authors at 2 institutions in 1 country.

Kanika SuriDepartment of Bioengineering, Northeastern University, Boston, MA 02115, USA.
Jason A BubierThe Jackson Laboratory, Bar Harbor, ME 04609, USA.ORCID 0000-0001-5013-1234
Michael V WilesThe Jackson Laboratory, Bar Harbor, ME 04609, USA.
Leonard D ShultzThe Jackson Laboratory, Bar Harbor, ME 04609, USA.
Mansoor M AmijiDepartment of Pharmaceutical Sciences, Northeastern University, Boston, MA 02115, USA.
Vishnu HosurThe Jackson Laboratory, Bar Harbor, ME 04609, USA.
Jackson Laboratory · USNortheastern University · US

Funding

Shared Resource ManagementP30CA034196 · NCI · JACKSON LABORATORY · PI Paul Robson · 1985 to 2026
$61.9M
Humanized Mouse Avatars for T1DU01DK104218 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI BREHM, MICHAEL ALLEN, GREINER, DALE LESLIE · 2019 to 2023
$4.5M
Genetic Variation in Opioid Induced Respiratory Depression in MiceR01DA048890 · NIDA · JACKSON LABORATORY · PI BUBIER, JASON A · 2020 to 2024
$3.4M
Development and Validation of a Novel Cas13a and Nanoparticle Guide-RNA Delivery System that Allows Precise Ablation of Host Macrophage Populations in a Humanized Mouse ModelR21OD027052 · OD · JACKSON LABORATORY · PI WILES, MICHAEL VAN · 2019 to 2020
$480k
NCI NIH HHS CA034196
6 · The paper itself

Abstract

The dysregulation of microRNA (miRNA) is implicated in cancer, inflammation, cardiovascular disorders, drug resistance, and aging. While most researchers study miRNA's role as a biomarker, for example, to distinguish between various sub-forms or stages of a given disease of interest, research is also ongoing to utilize these small nucleic acids as therapeutics. An example of a common pleiotropic disease that could benefit from miRNA-based therapeutics is inflammatory bowel disease (IBD), which is characterized by chronic inflammation of the small and large intestines. Due to complex interactions between multiple factors in the etiology of IBD, development of therapies that effectively maintain remission for this disease is a significant challenge. In this review, we discuss the role of dysregulated miRNA expression in the context of clinical ulcerative colitis (UC) and Crohn's disease (CD)-the two main forms of IBD-and the various preclinical mouse models of IBD utilized to validate the therapeutic potential of targeting these miRNA. Additionally, we highlight advances in the development of genetically engineered animal models that recapitulate clinical miRNA expression and provide powerful preclinical models to assess the diagnostic and therapeutic promise of miRNA in IBD.

Indexed as

AnimalsBiomarkersColitis, UlcerativeCrohn DiseaseDisease Models, AnimalGene ExpressionGene Expression RegulationHumansInflammationInflammatory Bowel DiseasesMiceMicroRNAsBiomarkersMicroRNAscollaborative crossCrohn’s disease (CD)diversity outbredextracellular vesiclesgenetic diversityhumanized miceIBDmiRNAulcerative colitis (UC)

Identifiers

PMID34571853
PMCPMC8468560
OpenAlexW3193634919

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.