Evidence map›Paper›PMID 25317587›Full record

ArticleThe Biochemical journal2015

Modulation by miR-29b of intestinal epithelium homoeostasis through the repression of menin translation.

Miao Ouyang, Weijie Su, Lan Xiao, Jaladanki N Rao, Liping Jiang, Yanwu Li, Douglas J Turner, Myriam Gorospe, Jian-Ying Wang

RetractedOpen access · hybridAbstract readRetracted Publication
In one paragraph

Article in The Biochemical journal, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.0field-weighted citation impact, top 25% 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, 26 citations in OpenAlex.

  1. Review
  2. Posttranscriptional Regulation of Intestinal Mucosal Growth and Adaptation by Noncoding RNAs in Critical Surgical Disorders.Journal of investigative surgery : the official journal of the Academy of Surgical Research · 2024
    Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. TRPC1-mediated CaPhysiological reports · 2021
    Article
  9. Arginine Metabolism and Its Potential in Treatment of Colorectal Cancer.Frontiers in cell and developmental biology · 2021
    Review
  10. Article
  11. Article
  12. Article
  13. Epigenetic regulation by the menin pathway.Endocrine-related cancer · 2017
    Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Miao Ouyang*Cell Biology Group, Department of Surgery, University of Maryland School of Medicine, Baltimore, MD, U.S.A.
Weijie Su*Cell Biology Group, Department of Surgery, University of Maryland School of Medicine, Baltimore, MD, U.S.A.
Lan Xiao*Cell Biology Group, Department of Surgery, University of Maryland School of Medicine, Baltimore, MD, U.S.A.
Jaladanki N Rao*Cell Biology Group, Department of Surgery, University of Maryland School of Medicine, Baltimore, MD, U.S.A.
Liping Jiang*Cell Biology Group, Department of Surgery, University of Maryland School of Medicine, Baltimore, MD, U.S.A.
Yanwu Li*Cell Biology Group, Department of Surgery, University of Maryland School of Medicine, Baltimore, MD, U.S.A.
Douglas J Turner*Cell Biology Group, Department of Surgery, University of Maryland School of Medicine, Baltimore, MD, U.S.A.
Myriam Gorospe‡Laboratory of Genetics, National Institute on Aging-IRP, National Institutes of Health, Baltimore, MD, U.S.A.
Jian-Ying Wang*Cell Biology Group, Department of Surgery, University of Maryland School of Medicine, Baltimore, MD, U.S.A.
University of Maryland, Baltimore · USInstitute on Aging · US

Funding

Post-transcriptional Regulation Of Proliferative and Stress Response GenesZIAAG000511 · NIA · NATIONAL INSTITUTE ON AGING · PI GOROSPE, MYRIAM · 2009 to 2025
$25.4M
Intestinal Mucosal Growth in Health & Surgical DiseasesR01DK057819 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI Jian-Ying Wang · 2000 to 2026
$7.4M
Surgical Studies of Gut PermeabilityR01DK068491 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI Jian-Ying Wang · 2004 to 2026
$7.0M
Mucosal Repair in Gut Surgical DisordersR01DK061972 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI WANG, JIAN-YING · 2002 to 2023
$6.7M
Barrier Dysfunction in Severe Surgical DiseasesI01BX000113 · VA · BALTIMORE VA MEDICAL CENTER · PI TURNER, DOUGLAS J · 2009 to 2024
–
REGULATION OF INTESTINAL EPITHELIAL RESTITUTIONI01BX000332 · VA · BALTIMORE VA MEDICAL CENTER · PI Jian-Ying Wang · 2009 to 2026
–
BLRD VA I01 BX000113BLRD VA I01 BX000332Intramural NIH HHSNIDDK NIH HHS DK57819NIDDK NIH HHS DK61972NIDDK NIH HHS DK68491NIDDK NIH HHS R01 DK057819NIDDK NIH HHS R01 DK061972NIDDK NIH HHS R01 DK068491
6 · The paper itself

Abstract

Menin regulates distinct cellular functions by regulating gene transcription through its interaction with partner transcription factors, but the exact mechanisms that control menin levels remain largely unknown. In the present study we report that Men1 mRNA, encoding menin, is a novel target of miR-29b and that miR-29b/Men1 mRNA association regulates menin expression post-transcriptionally in rat intestinal epithelial cells (IECs). Overexpression of a miR-29b precursor lowered the levels of Men1 mRNA modestly, but reduced new synthesis of menin robustly; conversely, antagonism of miR-29b enhanced menin protein synthesis and steady-state levels. The repressive effect of miR-29b on menin expression was mediated through a single binding site in the coding region of Men1 mRNA, because point mutation of this site prevented miR-29b-induced repression of menin translation. Increasing cellular polyamines due to overexpression of ornithine decarboxylase (ODC) enhanced menin translation by reducing miR-29b, whereas polyamine depletion by inhibiting ODC increased it, thus suppressing menin expression. Moreover, an increase in menin abundance in an miR-29b-silenced population of IECs led to increased sensitivity to apoptosis, which was prevented by silencing menin. These findings indicate that miR-29b represses translation of Men1 mRNA, in turn affecting intestinal epithelial homoeostasis by altering IEC apoptosis.

Indexed as

AnimalsApoptosisBiogenic PolyaminesCell LineGene Expression RegulationGene SilencingIntestinal MucosaMicroRNAsOrnithine DecarboxylaseProtein BiosynthesisRatsRNA, MessengerTranscription FactorsBiogenic PolyaminesMen1 protein, ratMicroRNAsMIRN29 microRNA, ratOrnithine DecarboxylaseRNA, MessengerTranscription Factors

Identifiers

PMID25317587
PMCPMC4286465
OpenAlexW2005896584

What OpenQuestion holds

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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.