Evidence map›Paper›PMID 31217548›Full record

ArticleScientific reports2019

Human endometriotic lesion expression of the miR-144-3p/miR-451a cluster, its correlation with markers of cell survival and origin of lesion content.

Warren B Nothnick, Kimberly Swan, Rebecca Flyckt, Tommaso Falcone, Amanda Graham

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

14 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
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  9. The Relationship and Expression ofInternational journal of molecular sciences · 2022
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  10. Article
  11. Review
  12. Review
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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

5 authors at 2 institutions in 1 country.

Warren B NothnickDepartment of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, KS, 66160, USA. wnothnic@kumc.edu.
Kimberly SwanDepartment of Obstetrics and Gynecology, University of Kansas Medical Center, Kansas City, KS, 66160, USA.
Rebecca FlycktDepartment of Obstetrics, Gynecology and Women's Health Institute, Cleveland Clinic, Cleveland, Ohio, 44195, USA.
Tommaso FalconeDepartment of Obstetrics, Gynecology and Women's Health Institute, Cleveland Clinic, Cleveland, Ohio, 44195, USA.
Amanda GrahamDepartment of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, KS, 66160, USA.
University of Kansas Medical Center · USCleveland Clinic · US

Funding

The Role of miR-451 in Endometriosis Pathophysiology and TreatmentR01HD069043 · NICHD · UNIVERSITY OF KANSAS MEDICAL CENTER · PI NOTHNICK, WARREN B · 2012 to 2016
$1.7M
Dissecting the functional role of miRNAs in decidualizationR21HD073733 · NICHD · UNIVERSITY OF KANSAS MEDICAL CENTER · PI NOTHNICK, WARREN B · 2013 to 2014
$410k
NICHD NIH HHS R01 HD069043NICHD NIH HHS R21 HD073733
6 · The paper itself

Abstract

Endometriosis is an inflammatory condition in which endometrial tissue grows in ectopic locations. Survival and growth of these ectopic lesions is associated with pain and infertility. MicroRNAs (miRNAs) have been postulated to play a role in the pathophysiology of the disease and we have previously demonstrated expression of miR-451 in human endometriotic lesion tissue. Here we report elevated expression of the miR-144-3p/miR-451a cluster in human endometriotic lesion tissue. Use of an endometriotic epithelial cell line (12Z) in which the miRNA processing enzyme, DROSHA, was knocked down resulted in an enrichment in the primary (pri) form of miR-144-3p but not that of pri-miR-451a. Using an experimental mouse model of endometriosis in which ectopic endometriotic lesions were deficient for both of these miRNAs revealed that miR-451a, but not miR-144-3p may be derived from exogenous sources such as the circulation/erythrocytes. Together, these data suggest that the miR-144-3p/miR-451a cluster is expressed in human endometriotic lesion tissue, the level of expression correlates with survival status of the lesion tissue and that miR-451a, but not miR-144-3p may be derived from exogenous sources such as erythrocytes.

Indexed as

Gene Expression RegulationAdultCell SurvivalEndometriumFemaleHumansMicroRNAsMiddle AgedRibonuclease IIIRNA, MessengerYoung AdultDROSHA protein, humanMicroRNAsMIRN144 microRNA, humanMIRN451 microRNA, humanRibonuclease IIIRNA, Messenger

Identifiers

PMID31217548
PMCPMC6584560
OpenAlexW2951684716

What OpenQuestion holds

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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.